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Redo att hitta din grej? Testa nytt, utbyt erfarenheter och upptäck vad du verkligen gillar att göra. Vi söker nu en medarbetare till sektionen Process Quality Engineering. Sektionen Process Quality ansvarar för att sätta krav och säkerställa efterlevnad av både externa och interna standarder inom sina specialistområden. Vi genomför industriella kvalificeringar, revisioner av speciella processer och driver kontinuerliga förbättringar kopplade till detta. Vidare ansvarar sektionen för teknikområden såsom oförstörande provning och svetsning samt tillhandahåller kompetens och resurser för vår mätutrustning på Saab. Din Roll I rollen kommer du att planera, genomföra och avsluta industriella kvalificeringar inom speciella processer, både hos leverantörer och inom Saabs egna produktionsenheter. Du blir en del av ett team tillsammans med våra Special Process Managers och Special Process Audit Leaders, där ni arbetar nära varandra och stöttar varandra i såväl strategiska som operativa frågor. Teamet präglas av samarbete, kunskapsdelning och en stark vilja att utvecklas tillsammans. Tillsammans har ni ett helhetsansvar för leveransen och bidrar med både teknisk kompetens och praktiskt genomförande. Rollen erbjuder även goda möjligheter att på sikt utvecklas mot att agera revisor inom specialprocesser. Du får en unik möjlighet att påverka och utveckla både ditt eget ansvarsområde och sektionens framtida arbetssätt. Rollen innebär många kontaktytor inom Aeronautics och Saab-koncernen samt samarbete med internationella leverantörer och verksamheter. Resor inom och utanför Europa ingår som en naturlig del av arbetet. Exempel på arbetsuppgifter: Planera industriella kvalificeringar i nära samarbete med bland annat Industrialisering, Inköp och Produktion. Genomföra kvalificeringar hos leverantörer och inom Saabs egna produktionsenheter samt driva uppföljning av identifierade åtgärder. Bidra till utveckling och förbättring av arbetssätt för planering, prioritering och genomförande. Utveckla och stärka samarbeten och gränssnitt inom Aeronautics och Saab Group. Bidra med specialistkunskap och stöd i frågor kopplade till speciella processer. Tillsammans skapar teamet en stark helhet där samarbete, kunskapsutbyte och gemensamt ansvar är avgörande för att nå framgång och säkerställa leverans. Din Profil Vi söker dig som trivs i en roll med många kontaktytor och som ser värdet i gott samarbete. Du är en lagspelare som gärna stöttar dina kollegor och som har lätt för att navigera mellan olika gränssnitt, både internt och externt. Eftersom rollen innebär samarbete med kollegor och leverantörer, både nationellt och internationellt, är du relationsskapande och bekväm i olika sammanhang. Rollen innebär resor till leverantörer samt deltagande i digitala möten, vilket ställer krav på att du är kommunikativ och trivs med att bygga och utveckla professionella relationer. Som person är du prestigelös, nyfiken och trygg i att samarbeta med erfarna specialister och experter. Du har hög integritet och en god förmåga att balansera ett konstruktivt samarbete med att säkerställa att krav, regelverk och processer efterlevs. Du är också tydlig i din kommunikation och kan på ett enkelt och pedagogiskt sätt presentera idéer, slutsatser och rekommendationer. Dessutom har du förmågan att självständigt skapa nya kontaktnät och bygga långsiktiga relationer. Vi tror att du har: Relevant arbetslivserfarenhet eller en akademisk examen inom ett för rollen passande område. Erfarenhet av produktionskvalitet eller speciella processer samt förståelse för tekniska krav, standarder och regelverk. God förmåga att samarbeta med både interna och externa intressenter. Goda kunskaper i svenska och engelska, i såväl tal som skrift. Det är meriterande om du har erfarenhet av revisionsverksamhet, men det är inget krav Befattningen kräver att du genomgår och godkänns enligt vid var tid gällande bestämmelser för säkerhetsskydd. För befattningar där Saab har krav på säkerhetsklassinplacering kan, i förekommande fall, medföra krav på visst medborgarskap. Vad du blir en del av Upptäck oändliga möjligheter. Anta utmaningar, skapa smarta innovationer och uppgradera dina förmågor. Det här är en plats för kluriga tänkare, modiga pionjärer och alla däremellan. Tillsammans uppnår vi det extraordinära, var och en tar med sitt unika perspektiv. Varje bidrag räknas. Saab är ett ledande försvars- och säkerhetsföretag med syfte att hjälpa nationer att skydda sin befolkning och bidra till trygghet för människor och samhällen. Med 28 000 talangfulla medarbetare utvecklar Saab teknik och lösningar för en säkrare och mer hållbar värld. Saab utvecklar, tillverkar och underhåller avancerade system inom flygteknik, vapen, ledningssystem, sensorer och undervattenssystem. Saab har sitt huvudkontor i Sverige men en global verksamhet där Saab är en del av många nationers försvarsförmåga. Läs mer om oss här. Med tanke på den kommande semesterperioden kan du förvänta dig återkoppling på din ansökan efter sommaren. Om du tycker att tjänsten låter intressant är du varmt välkommen att skicka in din ansökan redan idag!
Job Scope High level purpose of function. Responsible for the development, validation, and execution of the methods used for material analysis, including incoming material, intermediate, and finalized products for Research & Development and Production on a wide range of instruments. Strict adherence to the principles of Quality Assurance in Quality Control (QA/QC). Proven track record in statistical analysis and measurement system analysis (MSA). Key Responsibilities Overall areas of responsibilities and activities. Key responsibilities include (but are not limited to) Responsible for a set of instrumentation or measurement systems. This involves, but not limited to, coordinating maintenance and troubleshooting, writing support documentation, training and qualifying personnel, performing method development and validation. Understand and internalize QA/QC principles in everyday functions. Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples. Execute the Quality Control and testing plan of material and components. Maintaining instruments and measurement areas to a high standard, involving ownership of room(s)/area(s) to drive safety related topics, ensure 5S, maintain consumable inventory and standards/reference samples. Work across many parts of the organization, collaborating with R&D technical team, Process Quality Engineering, Process Engineering, Supply Chain, IT & automation. Drive operational excellence and investigations by being a key player in problem solving and process improvement exercises. Accountability/Authorization Budget responsibility: No Direct reports: No Work Environment responsibility: No All employees are accountable for complying with safety regulations and actively supporting a safe workplace. Requirements Educational background and previous experience required for the role. Qualifications and experience Minimum MSc degree or Bachelor’s degree with 5+ years of work experience in a laboratory, in Chemistry, Material or Mechanical Engineering. 3+ years of relevant work experience in relevant laboratory environment. Experience of laboratory work in relevant industries such as, e.g. Li-ion materials, Pharmaceutical, Food and Paper industries or automotive industries. Experience in developing methods, standards, procedures, and documentation in an efficient way. Familiarity with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma , Quality troubleshooting tools and problem-solving methodology. Specific skills & Knowledge Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. Knowledgeable in Laboratory Information Management System (LIMS), quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM). Project management skills and a successful track record of leading quality projects in a laboratory environment. Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams.
The European Spallation Source (ESS) will soon be the world’s most powerful source of neutrons, providing researchers with unique opportunities to explore the structure of materials at the atomic level. Neutron scattering at ESS will address critical questions in physics, chemistry, geology, materials science and life science. About the Role: ESS is at an exciting turning point, transitioning from a construction site to an operating facility. To help us achieve our goal of becoming the world’s most powerful neutron source, we are seeking a Process Engineer for the Plant & Process Engineering Function, part of the Design & Engineering Division. The team is responsible for maintaining state-of-the-art process activities across ESS. The group will first specify and design process systems such as cooling systems, instrument air and deionized water distribution, in accordance with PED, European harmonized codes, ESS rules and AFS regulations. They will then design the associated piping systems and mechanical supports to prepare for manufacturing, purchasing and installation phases. Finally, the group will help finalize the as-built documentation. Additional tasks include configuring and supporting the AVEVA tool suite, providing engineering review support, and offering technical advice. Day-to-Day you will: Perform system/project preliminary design based on design descriptions and requirements: Prepare specifications and reports, Review design projects, Prepare for and present at preliminary design reviews. Participate in critical process reviews, Document design and group development: Write and/or review process quality requirements, Write and/or review processing licensing requirements, Support standardization activities (components, best practices, and attributes), Propose and implement improvements to procedures, best practices, and policies. Follow up on post-design stages: Support manufacturing phases, Support installation and testing of equipment, Support as-built activities, Stay current with state-of-the-art technology. This is a full-time/permanent position based at the brand new https://www.youtube.com/watch?v=d5h4bIEfM5Q. About you: Required: Higher vocational education or university degree in engineering (e.g. a bachelor’s degree), or an equivalent combination of education and experience, Knowledge of components and system dimensioning for requirement and system/function descriptions, Proficiency in the AVEVA tool suite, Proficiency in written and spoken English. Desirable: Knowledge of normative constrained environments, Knowledge of EN harmonized codes, preferably EN 13445 and EN 13480, Knowledge of the Pressurized Equipment Directive (PED), Knowledge of fluid distribution system installation. We’re looking for someone who is self-motivated, has a problem-solving mindset, is structured, takes responsibility, and adheres to instructions and procedures. To apply: A career at ESS gives you the opportunity to contribute to the future discoveries within neutron science at a stunning, brand-new workplace filled with innovative minds and brilliant people from across the globe. We offer market competitive, individualised compensation which is differentiated according to role, responsibilities, individual skills, abilities and achievements as well as monthly pension contributions on top of your salary. If you see yourself in what we’re looking for, please provide your CV and motivation letter in English by clicking on “apply” and following the instructions. Please be aware that we can only accept direct applications made via the ESS website, so submit your application as soon as you can. The last date for receiving applications is 2026-07-26. For further information regarding the position, please contact Talent Acquisition Specialist Sofie Berg on mailto:sofie.berg@ess.eu or Hiring Manager Xavier Roy on mailto:xavier.roy@ess.eu Due to summer vacations questions will be answered after last application day, and first interviews will be conducted during week 34. This role requires enhanced security screening processes which will be performed during the recruitment and onboarding processes. For more information regarding the ESS recruitment process in general, please follow this link: https://europeanspallationsource.se/careers For trade union information, please contact Unionen representative Nerusha Naicker on mailto:Nerusha.Naicker@ess.eu or SACO/Swedish Association of Graduate Engineers representative Marc Kickulies at mailto:Marc.Kickulies@ess.eu
Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry. Assignment Description We are looking for a Senior Production Engineer What You Will Work On Develop and improve assembly processes and manufacturing methods Create and optimize work instructions and production standards Develop and maintain PFMEA (Process Failure Mode and Effects Analysis) Ensure production equipment, tools, and resources are available and properly utilized Support daily manufacturing operations together with operators and line technicians Drive production improvement initiatives and corrective actions Collaborate with line managers and cross-functional support teams Analyze production issues and implement sustainable solutions Improve productivity, quality, delivery performance, and workplace safety Support industrialization and process optimization activities Contribute to Lean Manufacturing and operational excellence initiatives Participate in continuous improvement and problem-solving activities Ensure manufacturing processes meet operational and business objectives What You Bring Minimum 5 years of experience as a Production Engineer Experience from manufacturing and industrial production environments Strong knowledge of assembly manufacturing processes Experience developing manufacturing methods and production workflows Experience working with PFMEA and process quality methodologies Knowledge of ERP systems Experience with production analysis and problem-solving Fluent Swedish and English, written and spoken
Location: Stockholm | Reports to: CFO | Employment type: Full-time Join Minnovation as our Senior Accountant Minnovation is looking for an experienced and hands-on Senior Accountant to join our finance team in Stockholm. This is a key role for someone who enjoys high-quality accounting, structured closing processes, statutory compliance and continuous improvement in an international and entrepreneurial environment. As Senior Accountant, you will take ownership of core accounting routines for Minnovation’s Swedish entities and support selected group accounting activities. You will work closely with the CFO and collaborate with colleagues, payroll providers, auditors, banks and external authorities to ensure accurate, timely and compliant financial reporting. About Minnovation Minnovation is an international HR consulting and business services company headquartered in Stockholm. We support companies and individuals across the Nordic region and wider European markets with services including staffing, recruitment, training, outsourcing, workforce administration and related business support. With a multicultural team and strong experience from Europe, the Nordic region and China, we help customers navigate employment, administration, finance and cross-border business requirements. About the role In this role, you will be responsible for accurate day-to-day accounting, monthly and year-end closing, balance sheet reconciliations, VAT and tax-related reporting, payroll accounting support, audit documentation and process quality. The role is operational and detail-oriented, but also offers the opportunity to improve routines, strengthen internal controls and contribute to better finance processes as the company continues to grow. Key responsibilities Own and maintain accurate accounting records for Minnovation’s Swedish entities. Lead monthly, quarterly and year-end closing activities, including journal entries, accruals, prepayments, cut-off checks and closing documentation. Prepare and document balance sheet reconciliations, including bank, AR, AP, tax, payroll-related and intercompany accounts. Prepare VAT, employer tax and other recurring statutory reports in line with Swedish requirements. Support payroll accounting by reconciling salary costs, employer contributions, vacation pay, pension-related costs and other personnel-related balances. Manage bank reconciliations, payment administration and cash-balance follow-up. Prepare accounting schedules, audit files and supporting documentation for external audits, annual accounts and tax reviews. Support group accounting routines, including intercompany reconciliations, basic consolidation input and reporting package preparation. Support budgeting, forecasting and cash-flow follow-up by providing accurate accounting data and explanations of key variances. Improve accounting routines, closing checklists, reconciliation standards and internal control procedures. Who we are looking for We are looking for a structured, accurate and self-driven accounting professional who enjoys taking ownership of recurring finance processes and improving how things are done. You are comfortable working hands-on with detailed accounting tasks while also understanding the bigger picture behind financial reporting, compliance and internal control. Qualifications and experience Bachelor’s or Master’s degree in Accounting, Finance, Business Administration or a related field. Minimum 5 years of qualified accounting experience, preferably including month-end and year-end closing in a Swedish company or group environment. Solid knowledge of Swedish accounting rules and statutory reporting requirements, including Swedish GAAP, K2/K3, the Swedish Annual Accounts Act, VAT, employer taxes and annual accounts. Experience with general ledger accounting, balance sheet reconciliations, accruals, prepayments, cut-off, AR/AP processes, bank reconciliations and audit preparation. Experience with payroll accounting, personnel cost reconciliations and cooperation with payroll providers is highly desirable. Experience from a group structure, international environment, service business, staffing, consulting, payroll or outsourcing/EOR-related operations is an advantage. Strong system skills, including accounting or ERP systems such as Visma or equivalent, and advanced Excel skills. Excellent written and spoken Swedish and English; Chinese or another relevant language is an advantage but not required. Personal skills Strong accounting judgement and ability to identify risks in balances, cut-off, accruals, tax reporting and payroll-related accounts. High attention to detail, accuracy and documentation quality. Structured and process-oriented, with the ability to improve routines, checklists and internal controls. Hands-on, self-driven and comfortable working independently. Analytical and able to explain accounting variances and financial issues clearly. High integrity and discretion when handling confidential financial, payroll, employee and customer-related information. Collaborative and service-minded, with the ability to work effectively with internal and external stakeholders. What we offer A key finance role in an international and growing HR consulting and business services company. Close collaboration with the CFO and exposure to both Swedish and international finance topics. A broad and hands-on accounting role with real ownership of closing quality, reconciliations and statutory compliance. The opportunity to improve finance routines, strengthen internal controls and contribute to more efficient processes. A multicultural working environment with colleagues and customers across several markets.
Are you an organized and detail-oriented professional looking to take the next step in your career? We are now looking for a Document Controller to join our client’s team! This is a great opportunity for you who want to work in a structured and coordinating role within an exciting and dynamic industry. Apply today – we work with ongoing selection! About the role As a Document Controller, you will play a key role in managing and organizing project documentation, ensuring compliance with company and regulatory standards. You will work closely with project managers, engineers, vendors, and contractors to ensure that all documentation is handled efficiently. You will be employed by Academic Work and work as a consultant at our client’s office. There are good opportunities for a long-term role and career development within the company. You are offered A role where you will be at the center of project execution, ensuring smooth documentation processes. The chance to work in a structured and international environment, collaborating with multiple departments. A dedicated Consultant Manager at Academic Work who will support you throughout your assignment. Work tasks Documentation Management & Organization – Handle collection, organization, categorization, and maintenance of all project documentation, ensuring compliance with company and regulatory standards. Version & Compliance Control – Track document versions, ensure adherence to company processes, regulatory requirements, and legal frameworks, including the Swedish Protective Security Act. Stakeholder & Vendor Coordination – Collaborate with project managers, engineers, vendors, and suppliers to facilitate smooth document flow and ensure the availability of necessary documentation. Process & Quality Assurance – Maintain and update document control procedures, manage transmittals, support users in adhering to document management processes, and ensure documentation quality. Project Handover & Technical Updates – Assist in project handover, oversee external documentation integration, estimate effort for future projects, and support engineering teams in updating technical standards. We are looking for Someone who has a degree in engineering, information management, or business administration. Previous experience in document control or a similar administrative role. Strong communication skills in Swedish and English. Strong communication skills to interact with various departments. Excellent organizational skills and attention to detail. Is proficient in document management software. This role is essential for maintaining the integrity and accessibility of project documentation, contributing to the overall success of engineering projects. If you have a keen eye for detail and excellent coordination skills, we encourage you to apply! To succeed in the role, your personal skills are: Trustful Supportive Social Respectful Our recruitment process This recruitment process is handled by Academic Work and it is our client’s wish that all questions regarding the position is directed to Academic Work. Our selection process is continuous and the advert may close before the recruitment process is completed if we have moved forward to the next phase. The process includes two tests: one personality test and one cognitive test. The tests are tools to find the right talent for the right position, to enable equality, diversity, and a fair process.
The opportunity We are looking for a Quality Specialist or Quality Engineer to join GI MACH in Sweden. MACH is a modular advanced control system for control and protection functions. MACH have approximately 500 employees developing electronics hardware and software. You will be a part of a small team responsible for Quality assurance, Process Governance and Product Reliability, which support the MACH organization with specialist competence within Quality. You have a solid background within Quality and knowledge from project management. You will in close cooperation with hardware and software engineers, create good practices and streamline the proactive quality process within R&D. It is an advantage if you have additional experience from software quality processes. If you want to take the next step in your career and contribute to develop a stronger, smarter, and greener energy system, then join us now! We are interested to learn more about you and what you can contribute so don’t hesitate to apply even if you don’t meet all the requirements. How you’ll make an impact Supporting the organization in driving improvement activities preventing quality issues Proactively evaluate and develop quality processes, measure quality activities, review and coordinate quality assurance activities Process governance and follow up of process adherence Promoter of a positive and proactive quality culture within MACH Continuous improvement driver to enhance development and product quality Perform internal audits and support in external audits Quality support and assurance of product development following Gate Model Your background Quality background is required – preferable within R&D. Engineer degree is not required if you have equal work experience within quality and R&D Demonstrated knowledge within Processes and management systems based on process methods Demonstrated knowledge of quality assurance and continuous improvement methods & approaches Six Sigma Yellow belt or 8D, DMAIC, PDCA skills Communication skills, ability to build trust on all levels of the organization Skills in MS Office and common quality management software Adonis process tool knowledge is meritorious Software or electronics background is meritorious Internal auditor and ISO 9001 background is meritorious Knowledge within FMEA methods and standards is meritorious More about us We offer you the opportunity to work with fantastic people and develop yourself on projects that present great technical challenges and have a real impact. Recruiting Manager Esbjorn Johansson, esbjorn.johansson@hitachienergy.com will answer your questions about the position. Union representatives - Sveriges Ingenjörer: Mikael Hjort, +46 107-38 29 86; Unionen: Fredrik Holmgren, +46 107-38 21 85; Ledarna: Frank Hollstedt, +46 107-38 70 43.
Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality. Key Responsibilities Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics Author and continuously improve SQE processes, work instructions, and templates Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required Perform other tasks as assigned by the Senior Manager Supplier Quality Requirements Educational background and previous experience required for the role BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline Qualifications and Experience ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory) Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R) Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production Specific skills & Knowledge Excellent English written and oral communication skills Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå
Are you a rehabilitation medicine consultant with expertise in neurological rehabilitation looking for an exciting opportunity in Ireland? On behalf of a well-established healthcare provider in Ireland, we are seeking experienced rehabilitation medicine consultants with expertise in neurological rehabilitation from Denmark, Ireland, Malta, or the United Kingdom for 6 to 12-month positions, with the possibility of extension. This is a unique opportunity to join a highly specialised neurorehabilitation service with a strong focus on multidisciplinary collaboration, patient-centred care and professional development. About the position As a Rehabilitation Medicine Consultant, you will be responsible for the assessment, diagnosis, treatment planning and ongoing management of patients requiring specialised neurological rehabilitation services. You will work with patients requiring complex rehabilitation following neurological injury and illness, helping them achieve the highest possible level of independence and quality of life. Typical responsibilities Assessment and management of patients requiring specialist neurological rehabilitation Developing individualised rehabilitation programmes Leading multidisciplinary team discussions Clinical decision-making and treatment planning Supporting patients and families throughout the rehabilitation process Contributing to quality improvement initiatives and service development We are looking for candidates who Are a consultant in rehabilitation medicine with expertise in neurological rehabilitation Hold specialist certification and medical registration from Denmark, Ireland, Malta or the United Kingdom Have solid experience working within rehabilitation services Have excellent English language skills, both spoken and written Communicate clearly and confidently with patients and colleagues Maintain a high professional standard with strong attention to quality and patient experience Enjoy working in multidisciplinary teams focused on delivering high-quality rehabilitation services We offer Contract for 6-12 months, with the possibility of extension The opportunity to work in a highly specialised rehabilitation environment Modern facilities and a highly professional clinical team Competitive salary and attractive employment conditions Close follow-up throughout the recruitment process Assistance with registration and relocation The opportunity to visit Ireland before making a decision and get to know the hospital and the area Salary The annual gross salary depends on experience and is approximately €235,000–285,000 per year. Why Ireland? Working in Ireland gives you the opportunity to practice medicine in an English-speaking healthcare system while gaining valuable international experience. You will work in a collaborative clinical environment with modern facilities and a strong focus on patient care. Beyond work, Ireland offers a high quality of life and a welcoming atmosphere. The country is known for its dramatic coastline, green landscapes and charming towns. Ireland also has a lively social culture, where local pubs often serve as gathering places for music, conversation and community. Interested? Please feel free to contact us if you would like to learn more about the position or the recruitment process. We would be happy to tell you more about the clinic, the working environment and the opportunities available.
We are looking for an engaging person who wants to grow together with their team and the company. You will be responsible for managing one of our software design and integration teams within the HVDC Control & Protection Software area. The team is responsible for supplying control and protection solutions for HVDC projects across the globe including software design, development, integration, testing and verification in real-time and virtual environments. “A unique opportunity to be part of an extremely growing and flourishing organization at a company that is at the forefront and holds the number one market position”- Erik Kilander, Global Manager HVDC Control and Protection Software. How you’ll make an impact Through Managing a team of system engineers with responsibility of HVDC control and protection software involving design, integration and testing in both virtual and real-time systems. Being the owner of the technical function area with responsibility of process adherence and quality assurance Establishing and maintain alignment, collaboration, and system support towards neighbouring departments Being a positive role model for your team by living our vision, delivering promises, and developing people. Adapting and implementing strategic initiatives to fit your team to achieve business alignment. Planning team composition, development and capabilities needed to meet business needs, in alignment with internal stakeholders and customers. Your background You have at least a university degree in Engineering, or equivalent experience from a comparable position To successfully take on this position, you probably have experience from supporting and growing team members in an environment with continuously upcoming opportunities and challenges. You’ll assess essential aspects of the business and make informed choices in line with the business requirements. A motivated leadership is required for this role since the change process takes time and is challenging. Good communication skills in Swedish and English, both written and verbal. High level of time management skills for you self and when coaching others. What we offer Collective agreement Flexible working time Health care and wellness allowance Fantastic career possibilities within Hitachi Energy both within Sweden and globally Mentor to support you throughout onboard phase Various trainings and education supporting employee development Diversified company with over 70+ nationalities working in Sweden Supplementary compensation for parental leave Employee Benefit Portal with thousands of discounts and perks More about us Are you ready for a new exciting challenge? Does the above description sound like you? Welcome to apply! Applications will be reviewed on an ongoing basis, so don’t delay – apply today! Recruiting Manager Erik Kilander, erik.kilander@hitachienergy.com will answer your questions about the position. Union representatives – Sveriges Ingenjörer: Mikael Hjort, +46 107-38 29 86; Unionen: Fredrik Holmgren, +46 107-38 21 85; Ledarna: Frank Hollstedt, +46 107-38 70 43. All other questions can be directed to Talent Acquisition Partner Magnus Rönnholm, magnus.ronnholm@hitachienergy.com.
Are you a rehabilitation medicine consultant looking for an exciting opportunity in Ireland? On behalf of a well-established healthcare provider in Ireland, we are seeking experienced Rehabilitation Medicine Consultants from Denmark, Ireland, Malta, or the United Kingdom for 6 to 12-month positions, with the possibility of extension. This is a unique opportunity to join a highly specialised rehabilitation service with a strong focus on multidisciplinary collaboration, patient-centred care and professional development. About the position As a Rehabilitation Consultant, you will be responsible for the assessment, diagnosis, treatment planning and ongoing management of patients requiring specialised rehabilitation services. You will work closely with physiotherapists, occupational therapists, speech and language therapists, rehabilitation nurses, psychologists and social care professionals to ensure coordinated and patient-centred care. Typical responsibilities Assessment and management of patients requiring specialist rehabilitation Developing individualised rehabilitation programmes Leading multidisciplinary team discussions Clinical decision-making and treatment planning Supporting patients and families throughout the rehabilitation process Contributing to quality improvement initiatives and service development The rehabilitation service has particular expertise within Neurological rehabilitation Age-related rehabilitation Respiratory rehabilitation Rheumatology rehabilitation We are looking for candidates who Are a consultant in rehabilitation medicine Hold specialist certification and medical registration from Denmark, Ireland, Malta or the United Kingdom Have solid experience working within rehabilitation services Have excellent English language skills, both spoken and written Communicate clearly and confidently with patients and colleagues Maintain a high professional standard with strong attention to quality and patient experience Enjoy working in multidisciplinary teams focused on delivering high-quality rehabilitation services We offer Contract for 6-12 months, with the possibility of extension The opportunity to work in a highly specialised rehabilitation environment Modern facilities and a highly professional clinical team Competitive salary and attractive employment conditions Close follow-up throughout the recruitment process Assistance with registration and relocation The opportunity to visit Ireland before making a decision and get to know the hospital and the area Salary The annual gross salary depends on experience and is approximately €235,000–285,000 per year. Why Ireland? Working in Ireland gives you the opportunity to practice medicine in an English-speaking healthcare system while gaining valuable international experience. You will work in a collaborative clinical environment with modern facilities and a strong focus on patient care. Beyond work, Ireland offers a high quality of life and a welcoming atmosphere. The country is known for its dramatic coastline, green landscapes and charming towns. Ireland also has a lively social culture, where local pubs often serve as gathering places for music, conversation and community. Interested? Please feel free to contact us if you would like to learn more about the position or the recruitment process. We would be happy to tell you more about the clinic, the working environment and the opportunities available.
At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the industry. Every day, more than 80 000 colleagues lead the way to greener and smarter mobility worldwide, connecting cities as we reduce carbon and replace cars. Your future role Take on a new challenge and apply your organizational and analytical expertise in a cutting-edge field. You’ll work alongside collaborative and detail-oriented teammates. You'll play a key role in supporting procurement operations, ensuring accuracy and compliance while contributing to process improvements. Day-to-day, you’ll work closely with teams across the business (procurement, finance, and vendor management), assist in maintaining vendor records, and help analyze procurement performance data, among other responsibilities. You’ll take care of vendor and supplier management tasks, but also support invoicing, payment processes, and purchase order management. We’ll look to you for Supporting day-to-day activities related to invoicing and payment management systems Assisting in reviewing and updating incomplete or inaccurate supplier information Helping maintain vendor records in procurement systems in line with established processes Assisting in identifying data inconsistencies and escalating issues to relevant stakeholders Contributing to purchase order management, including data cleaning and closing obsolete contracts Supporting basic data analysis related to procurement performance and vendor data Assisting in preparing and maintaining KPI and compliance tracking reports Ensuring adherence to Group procurement policies and governance requirements Contributing to continuous improvement of procurement data quality and process efficiency All about you We value passion and attitude over experience. That’s why we don’t expect you to have every single skill. Instead, we’ve listed some that we think will help you succeed and grow in this role: Currently pursuing a Bachelor’s degree in Business Administration, Supply Chain Management, Procurement, Finance, Data Analytics, or a related discipline Strong attention to detail and interest in data accuracy Basic understanding or strong interest in procurement processes (vendors, POs, invoices, payment terms, Incoterms) Willingness to learn data cleaning and basic data analysis Basic proficiency in Microsoft Office, particularly Excel (filters, basic formulas, pivot tables are a plus) Good communication and follow-up skills Ability to manage multiple tasks and timelines with guidance Organized, proactive, and willing to learn Comfortable working with systems and structured processes Team-oriented with a positive and professional attitude Strong English communication skills – able to communicate professionally in both spoken and written English in the international environment Things you’ll enjoy Join us on a life-long transformative journey – the rail industry is here to stay, so you can grow and develop new skills and experiences throughout your career. You’ll also: Enjoy stability, challenges, and a long-term career free from boring daily routines Work with enterprise systems like SAP and invoicing platforms Collaborate with transverse teams and helpful colleagues Contribute to innovative projects that shape the future of mobility Utilise our structured and supportive working environment Steer your career in whatever direction you choose across functions and countries Benefit from our investment in your development, through award-winning learning Progress towards potential roles in procurement, supply chain, operations, or data analytics Benefit from a fair and dynamic reward package that recognises your performance and potential, plus comprehensive and competitive social coverage (life, medical, pension) You don’t need to be a train enthusiast to thrive with us. We guarantee that when you step onto one of our trains with your friends or family, you’ll be proud. If you’re up for the challenge, we’d love to hear from you! Important to note As a global business, we’re an equal-opportunity employer that celebrates diversity across the 63 countries we operate in. We’re committed to creating an inclusive workplace for everyone.
Haldex is a leading manufacturer of reliable and innovative braking systems and air suspension solutions that improve safety, dynamics and durability for heavy vehicles. Design Engineer – Valves We are looking for a Design Engineer to be a part of new product development as well as product maintenance within the valves and actuators product group. Part of your role is project oriented, and you will be an important part in project teams. Sometimes you will work on future concepts, innovation ideas not yet governed by any project. Working as a Design Engineer at Haldex, you will also interact cross functionally with other teams in different countries that is part of the SAF/Holland company group. At Haldex you will be a part of our R&D team with colleagues and internal stakeholders all around the world. Haldex has a flexible remote working policy, wellness subsidy & a gym at the site. Job description Development of new products mainly within the valves and actuator product group o Develop design solutions to meet required specification/s o Evaluate design solutions related to supplier process and internal assembly process with focus on the total cost solution. o Support the development of the product from conception through to manufacture and its maintenance. o Participate in technical discussions with suppliers and customers. o Create internal technical requirement specifications on product. o Support development of new test methods for new design elements/sub-systems. Product maintenance mainly within the valves and actuator product group o Improve and develop current products. o Understand and work according to Haldex Change Management Process for changes. Other o Review Customer product requirements. o Create and update technical specifications, i.e., drawings, models, calculations etc. o Analyze results from calculations and performed tests. o Take actions when faults are discovered both on product and in process. Support in quality related activities including root cause analysis (ex. 8D method). o Follow Haldex processes, and for design related processes continuous improvements as target. Education and Experiences § Minimum Bachelor of Science degree in Mechanical Engineering or equivalent. § At least three years experience of working with pneumatics § We expect that you have Material knowledge and knowledge of manufacturing methods. § A documented skill in a CAD system, preferably CREO. § Knowledge in PDM system and base knowledge in MathCAD. § Tolerance analysis using software or other methodology. § Base knowledge in Finite Element Analysis program, preferably ANSYS workbench. § Good knowledge in Office software applications. § English fluent verbally and in writing. Experiences of automotive industry, Heavy Truck / Bus experience is meritorious. Recommended is at least five years of design and/or validation experience, preferably within automotive industry. Personal characteristics You are an ambitious and curious person, passionate about technology and exploration of possibilities in tools and equipment. You are also driven and motivated to complete tasks and you have a structured way of working. You are used to work in cross functional teams, are service minded and you are humble, prestige less and a natural team player. Application Does this sound like something for you – or someone you know? Submit your application today! Selection is ongoing, and the final application deadline is September 7th. For questions about the position, contact Joakim Gripemark at joakim.gripemark@safholland.com. For questions about the process, contact HR Manager Elin Önnby at elin.onnby@safholland.com. Welcome with your application!
We are looking for an experienced RDMA Line Controller to join an international company experiencing strong growth. If you have solid experience in Business Controlling, a passion for finance business partnering, and a natural ability to navigate a complex, global organization - you are the one we are looking for! We review applications continuously, so do not hesitate to apply today. About the role Our client is looking for a dedicated RDMA Line Controller to take on a central and business-facing controlling role within Research, Development and Medical Affairs (RDMA). The organization manages an annual budget of several billion SEK, divided between project activities and the ongoing line organization, comprising approximately 200 employees and 100 cost centers across Europe, the US, and Japan. In this role, you will act as a financial business partner to several functional leaders, translating business plans into financial realities and creating transparency around performance. This is a dynamic role suited for someone who wants to combine qualified finance business partnering with clear operational responsibility in a complex global environment. You are offered A strong international network: Collaborate closely with global functional leaders, an international co-controller, and an experienced local network of finance professionals. Strategic and operational variety: A highly varied role where you move seamlessly between strategic discussions with senior leaders and hands-on Excel analysis, forecasting, and cost center management. High degree of ownership: The opportunity to independently drive and develop financial processes in a trust-based, collaborative culture. Work tasks Your responsibilities will include: Act as a financial business partner to functional leaders and senior stakeholders within RDMA. Develop a thorough understanding of business plans, priorities, resource requirements, and cost drivers. Constructively challenge budget owners' assumptions and plans, helping to identify practical solutions that balance scientific needs with available resources. Drive the four annual planning and forecasting cycles, including the budget process. Coordinate and quality-assure financial input from a large number of cost centers and business areas. Monitor actual performance against budget/forecast and analyze the underlying causes of variances. Identify financial risks and opportunities, explaining their impact on the full-year forecast. Take ownership of relevant month-end and quarter-end close activities (accruals, reallocations, and closing documentation). Collaborate with accounting, Business Controllers, System Controllers, and the wider global finance organization to improve processes and transparency. We are looking for Have at least 4-5 years of relevant experience in Business Controlling, Line Controlling, or Finance Business Partnering. Have extensive experience with budgeting, forecasting, financial planning, and performance management. Have proven experience independently supporting and challenging senior business leaders. Have a solid understanding of month-end closing, accruals, and other accounting-related controlling activities. Have strong analytical capabilities and advanced Excel skills. Are fluent in English, both spoken and written, as this is the primary working language. It is meritorious if you have God skills in Swedish Experience in the life science pharmaceutical, research, or other knowledge-intensive industries. Experience supporting R&D organizations or clinical studies, including project controlling. Experience with large ERP systems, financial reporting tools, or digital/AI-enabled automation in finance. To succeed in the role, your personal skills are: Structured Proactive Driven Communicative team payer Social Our recruitment process This recruitment process is handled by Academic Work and it is our client’s wish that all questions regarding the position is directed to Academic Work. Our selection process is continuous and the advert may close before the recruitment process is completed if we have moved forward to the next phase. The process includes two tests: one personality test and one cognitive test. The tests are tools to find the right talent for the right position, to enable equality, diversity, and a fair process.
Haldex is a leading manufacturer of reliable and innovative braking systems and air suspension solutions that improve safety, dynamics and durability for heavy vehicles. Haldex's customers are primarily major manufacturers of trucks, buses and trailers in North America, Europe and Asia. In the aftermarket, Haldex offers spare parts and service to distributors, workshops and large logistics companies. Haldex was founded in 1887 in Landskrona and has since distinguished itself through innovative research and development work that has created groundbreaking technical vehicle solutions. Development today is focused on safety and the future of electrified, autonomous and connected heavy vehicles. Haldex's operations are global with approximately 2,000 employees in 19 countries. Haldex a strong brand of SAF-HOLLAND group. Junior Design Engineer Are you at an early stage in your career? We are looking for a Design Engineer to be a part of new product development as well as product maintenance. In Landskrona we design and maintain four product groups; air disc brakes, automatic brake adjusters for drum brakes, valves and actuators. You can be involved in all four product groups. Part of your role is project oriented, and you will be an important part in project teams. Working as a Design Engineer at Haldex, you will also interact cross-functionally with other teams in different countries that are part of the SAF/Holland company group. At Haldex you will be a part of our R&D team with colleagues and internal stakeholders all around the world. Job description o Development of new products o Develop design solutions to meet required specifications o Evaluate design solutions related to supplier process and internal assembly process with focus on the total cost solution. o Support the development of the product from conception through to manufacture and its maintenance. o Participate in technical discussions with suppliers and customers. o Create internal technical requirement specifications on product. o Support development of new test methods for new design elements/sub-systems. Product maintenance o Improve and develop current products. o Understand and work according to Haldex Change Management Process for changes. Other o Review Customer product requirements. o Create and update technical specifications, i.e., drawings, models, calculations etc. o Analyze results from calculations and performed tests. o Take actions when faults are discovered both on product and in process. Support in quality related activities including root cause analysis (ex. 8D method). Education and Experiences § Minimum Bachelor of Science degree in Mechanical Engineering or equivalent. § We expect that you have Material knowledge and knowledge of manufacturing methods. § A documented skill in a CAD system, preferably CREO. § Knowledge in PDM system and base knowledge in MathCAD. § Tolerance analysis using software or other methodology. § Base knowledge in Finite Element Analysis program, preferably ANSYS workbench. § Good knowledge in Office software applications. § Fluent in English, verbally and in writing. Experiences of automotive industry, Heavy Truck/Bus experience is meritorious. Personal characteristics You are an ambitious and curious person, passionate about technology and exploration of possibilities in tools and equipment. You are also driven and motivated to complete tasks and you have a structured way of working. You are used to working in cross functional teams. You are service-minded, humble and a natural team player. Contact If you have any questions regarding the recruitmentprocess please contact HR Manager Elin.Onnby@safholland.com. We work continuously with the selection, so we want your application as soon as possible. Welcome with your application!
Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products. As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us! This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today. Key responsibilities The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO. Duties and responsibilities include: Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency. Lead root cause investigations and implement corrective and preventive actions (CAPA). Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification. Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results. Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why. Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles. Support audits and inspections by customers, regulatory authorities, and Notified Bodies. Support technology transfers from R&D to production and participate in cross-functional development projects. Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply. Skills and Competencies The suitable candidate has the following qualifications: Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related. Strong background in process engineering preferably combined with validation engineering experience. Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries). Experience with process optimization, process validation and problem solving. Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable. Experience working with Quality Management Systems. Knowledge of statistical analysis and process capability concepts. Excellent communication and documentation skills in English are required The successful candidate for this position will be someone who: Has a strong technical and analytical mindset. Enjoys solving complex manufacturing and process-related challenges. Is structured and detail-oriented. Takes ownership and drives improvements independently. Communicates effectively across departments and organizational levels. Combines hands-on problem solving with a systematic approach. Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important. We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development. About Bohus Biotech Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence. With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide. Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas: Ophthalmology – OVD solutions supporting tissue protection during cataract surgery Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform Orthopaedics – Injectable treatments for osteoarthritis All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com For more information about this position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: +46 (0)72-070 16 53 E: krishan.johansson-haque@qrios.se
Här får du möjligheten att kliva in i ett innovativt deep-tech bolag där forskning, utveckling och produktion sker sida vid sida – och där kvalitet är en avgörande del av att lyckas. Du blir en del av ett litet och engagerat team där du får arbeta nära både produktion, utveckling och industrialisering i en verksamhet som fortfarande befinner sig i en spännande uppbyggnadsfas. Det här är inte en traditionell kvalitetsroll i en färdig organisation med tydliga ramar och långa beslutsvägar. Här händer det mycket, beslut fattas snabbt och arbetet präglas av nyfikenhet, samarbete och viljan att tillsammans bygga något långsiktigt. För rätt person innebär det en möjlighet att påverka på riktigt och vara med och forma både arbetssätt och framtida struktur. Om tjänsten Som Quality Engineer kommer du att arbeta brett med kvalitetsfrågor kopplade till både process, produktion och produktutveckling. Ena dagen analyserar du produktionsdata och identifierar trender eller rotorsaker bakom avvikelser, nästa dag sitter du tillsammans med utvecklingsteamet och diskuterar hur kvalitet ska säkras i nästa steg av industrialiseringen. Rollen innebär många kontaktytor och du kommer att arbeta nära både forskare, ingenjörer, produktion och ledning. Miljön är datadriven och kvalitetsteamet arbetar aktivt med statistik, SPC och analysverktyg för att förstå processer och driva förbättringar framåt. Samtidigt handlar rollen minst lika mycket om kommunikation och samarbete – att kunna få med sig andra, skapa förståelse för kvalitet och bidra med struktur utan att bygga onödig byråkrati. Du kommer bland annat att arbeta med: Dataanalys, trenduppföljning och statistisk processtyrning Rotorsaksanalyser och förbättringsarbete Kvalitetsverktyg såsom RCA, PFMEA och DFMEA Process- och produktkvalitet nära produktionen Kund- och leverantörsrelaterade kvalitetsfrågor Att vidareutveckla kvalitetsprocesser och arbetssätt i takt med att bolaget växer Vi tror att du Har några års erfarenhet inom kvalitetsarbete i tillverkande industri och trivs i en miljö där teknik, produktion och problemlösning står i centrum. Du har sannolikt arbetat nära processer och produktion tidigare och känner dig bekväm med att använda data för att förstå problem och driva förbättringar. Vi tror också att du: Har erfarenhet av SPC och statistisk analys Har arbetat med kvalitetsverktyg som RCA, PFMEA eller DFMEA Har förståelse för QMS och kvalitetsarbete i industrimiljö Har en teknisk utbildningsbakgrund, gärna inom produktion, material, kemi eller liknande område Trivs i en dynamisk miljö där inte allt är helt färdigdefinierat Det är meriterande om du har erfarenhet av analysverktyg som JMP eller Minitab samt om du tidigare arbetat inom processindustri, materialteknik eller annan högteknologisk tillverkningsmiljö. Stor vikt kommer läggas vid personlighet och vi tror att du är en nyfiken, prestigelös och samarbetsorienterad person som gillar att ta ansvar och bidra där det behövs. Här hjälps man åt, arbetar tätt tillsammans och bygger vidare på verksamheten som team. Om företaget Bolaget är ett svenskt teknikföretag i framkant inom material- och energiteknologi. Här kombineras forskning, utveckling och produktion i en innovativ miljö där nya idéer snabbt kan omsättas till verklighet. Kulturen präglas av öppenhet, högt engagemang och viljan att tillsammans lösa komplexa tekniska utmaningar. För dig som gillar teknik, förändring och möjligheten att påverka erbjuder detta en unik chans att bli en del av en verksamhet där man verkligen gör skillnad – varje dag. Om anställningen Detta är en rekrytering där du blir anställd direkt hos kundföretaget. Rekryteringsprocessen hanteras av Friday och alla frågor kring tjänsten hänvisas till ansvarig rekryterare. Övrig info Omfattning: HeltidStart: Enligt överenskommelsePlacering: Kista, StockholmArbetssätt: 100 % på plats, med viss flexibilitetLön: Fast månadslön Ansök genom att klicka på länken nedan. Urval sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. Om Friday: På Friday hjälper vi Tech-talanger att hitta roller där de trivs, utvecklas och gör skillnad. Genom att lyssna på vad just du vill och drivs av, matchar vi dig med företag och möjligheter som får dig att se fram emot att gå till jobbet. Vi värderar ambition och potential högt och arbetar aktivt för en fördomsfri rekrytering, där alla ges samma chans att lyckas. Vi finns i Stockholm, Göteborg, Malmö, Linköping och Örebro. Varje år genomför vi över 5 000 karriärmöten och matchar kandidater med allt från globala företag till innovativa startups. Sökord: Quality Assurance, QA, Quality engineer
About the position Join Mycronic’s Pattern Generators Division as a Quality Engineer in the Metrology and Process Control group (PMCD). In this role, you will work with process quality, Statistical Process Control, and process optimization for advanced mask manufacturing used in the display and semiconductor industries. You will work close to the cleanroom, process equipment, metrology results, and R&D projects. The work combines data analysis, hands-on cleanroom processing, process tuning, and improvement of process control methods. You will support both daily process stability and new product development, with a focus on making our processes more stable, capable, and repeatable. Key Responsibilities include but are not limited to: • Drive and maintain SPC and process control, including monitoring process stability, setting control limits, analyzing trends, and improving process capability. • Work hands-on in the cleanroom with wet chemical and RIE processes, including developing, chrome etching, cleaning, tuning, troubleshooting, and process optimization. • Run and support both automated and manual mask processing, including operating process tools, performing manual process steps, refilling chemicals, and following cleanroom and safety routines. • Plan, run, and evaluate experiments to support R&D activities, including novel product development, process robustness, cleanliness, cleaning performance, and defect reduction. • Analyze process and metrology data to find trends, deviations, root causes, and improvement opportunities. • Support investigations related to yield, process variation, etch performance, uniformity, repeatability, cleanliness, and equipment-related process effects. • Create and improve documentation such as work instructions, process specifications, control plans, test plans, and quality routines. • Work closely with colleagues in process development, metrology, product development, production, system engineering, and quality. Qualifications Are you ready to help shape the future with us? Mycronic is the right place for you if you are driven, curious, and motivated by solving technical problems. To succeed in this role, you need a structured and analytical way of working, combined with a strong interest in hands-on process work. You should enjoy working in a cleanroom environment and be comfortable moving between practical processing, statistical analysis, troubleshooting, and technical discussions. You take responsibility for your work, pay attention to details, and want to understand why a process behaves in a certain way. Because the role includes frequent collaboration with other engineers, you should be a strong team player who can explain technical findings clearly and help turn data into practical improvements. On top of this, you need: • MSc or higher in Nanotechnology, Microfabrication, Semiconductor Processing, Physics, Chemistry, Materials Science, Chemical Engineering or related technical fields. • Experience with process optimization for chrome etch processes. • Experience from cleanroom work, preferably within semiconductor, photomask, display, MEMS, microfabrication, or similar advanced manufacturing. • Experience with SPC, process control, process capability, trend analysis, and data-based problem solving. • Practical experience with wet chemical processing, such as developing, etching, cleaning, or similar chemical process steps. • Good understanding of process variation, repeatability, stability, contamination control, and how process parameters affect product quality. • Ability to analyze complex technical problems and turn data into conclusions, actions, and improvements. • Willingness and ability to work hands-on in a cleanroom, including chemical handling and manual processing. • Fluent English, both written and spoken. It is a merit if you have: • Experience with RIE process development, tuning, troubleshooting, or process control. • Experience from photomask, semiconductor, display, MEMS, or advanced lithography-related manufacturing. • Experience with DOE, process windows, control plans, FMEA, root-cause analysis, or other structured engineering methods. • Experience using metrology data to understand and improve process performance. • Experience with cleanliness, cleaning processes, particle control, contamination analysis, or defect reduction. • Knowledge of chrome, quartz, glass, resist, or other materials used in mask manufacturing. • Experience supporting R&D projects or transferring processes from development into stable operation. Place of employment: Headquarters in Täby, right outside Stockholm, Sweden Application deadline: 2026-07-23 Contact person: David Luthman, Group Manager, david.luthman@mycronic.com. How to apply: Submit your CV via our portal A culture of collaboration and personal growth At Mycronic, we love what we do, but most importantly who we do it with. Because to us the relationships we have with our customers and each other are the keys to success. Take part in the excitement of working with innovative people and global businesses who are elevating today’s standards in modern electronics. Share in the responsibility of bringing great ideas to life within an inclusive culture that not only promotes personal growth and embraces diversity but depends upon it. Here you are expected to have a voice and will be encouraged to get involved. It’s this very mindset that empowers our people to make a positive difference for a broad range of businesses, society and the planet – every day. https://www.mycronic.com/en/career/working-at-mycronic/
Execute Precision Manufacturing at the Core of a Deep-Tech Scale-Up At Smart High Tech, we are transforming advanced materials into industrial production. Our graphene-based technology enables the next generation of AI systems, electronics and data centres, where performance depends on precision, quality and consistency. As we scale production, we are looking for Production Operators who take pride in executing critical manufacturing processes with accuracy, discipline and attention to detail. Your Mission You will play a key role in ensuring stable, safe and high-quality production. Your work directly impacts: Product quality Process stability Production efficiency What You Will DoProduction Operations Operate production equipment such as furnaces, coating lines and cutting machines. Perform material-handling, loading, and unloading activities. Ensure process parameters remain within defined specifications. Follow production schedules and work instructions. Quality & Process Control Monitor production performance and process conditions. Perform visual and dimensional quality inspections. Identify, report and escalate deviations. Support consistent product quality and process stability. Equipment & Maintenance Perform basic preventive maintenance and daily inspections. Maintain equipment cleanliness and operational readiness. Report technical issues and abnormalities to Maintenance. Documentation & Safety Register production data, material usage and quality observations. Ensure accurate and timely documentation. Maintain a clean, organised and safe work environment. Follow all safety procedures and operational standards. Key Interfaces You will work closely with: Production Leader Production Engineers Maintenance Team Quality Department Operations & Planning Who You Are You are reliable, quality-focused and enjoy working in a structured production environment. Required Qualifications Upper secondary education in Industrial Technology, Manufacturing or similar. Experience from manufacturing, production or process industries. Strong ability to follow instructions and work systematically. High focus on quality, safety and accuracy. Good communication skills in Swedish and English. Willingness to work shifts. Meritorious Experience operating furnaces, coating lines or similar process equipment. Experience from thermal processes, surface treatment or advanced manufacturing. Technical interest and basic mechanical understanding. Additional language skills. Why Join Smart High Tech? This is an opportunity to work with advanced manufacturing technologies in a fast-growing deep-tech company. You will: Be part of scaling innovative technology into global production. Work in a modern manufacturing environment with advanced processes. Receive support and training from experienced engineers and specialists. Contribute directly to product quality and operational success. Join a team where precision, responsibility and teamwork are highly valued. What Success Looks Like Within your first months, you have: Learned and mastered key production processes. Operated equipment independently and safely. Maintained stable output and quality standards. Contributed to efficient production and continuous improvement.
Are you an experienced Process Operator looking to bring your expertise to the next level? Briquette Operators are critical to our daily production at Stegra. Your experience, precision, and ability to keep systems running efficiently play a key role in ensuring we meet our performance goals and continue to improve. With your expertise, we strengthen the reliability and quality that set our plant apart in the industry. A bit about the role At Stegra, we’re not just building a plant, we’re proving that sustainable industry is possible. And to do that, we need people like you. As a Process Operator in the briquetting section of the DRI Plant you will play a critical role in ensuring the efficient and smooth operation of the briquetting process. Your responsibility is to monitor, control, and optimize production to ensure continuous operations and high-quality Hot Briquetted Iron (HBI). What you’ll do: Actively contribute to a safe work environment by following and promoting safety protocols and participating in process control improvements. Ensure briquetting process meets quality specifications and operational parameters for HBI production. Monitor, inspect, and maintain briquette machines, conveyors (metal and rubber), dust collection systems, and related equipment. Perform field operations, including starting and stopping briquette machines and carrying out roll-in, roll-out operations. Use control systems and safety tools such as Permit-to-Work (PTW) and Lockout/Tagout/Tryout (LOTOTO) systems. What you’ll bring: Experience in DRI plant briquette operations, including troubleshooting and problem-solving. Preferably hands-on experience in hot or cold briquetting processes. Experience working with conveyors, dust collection systems, and relevant mechanical equipment. Familiarity with operating in a safety-driven industrial environment using PPE correctly. High school diploma in a relevant field or equivalent education preferred. All relevant certificates required to perform the job. Oral and written proficiency in English is required; Swedish is considered an advantage. What you’ll get: If you're passionate about making a real difference and contributing to a more sustainable future, Stegra offers a unique opportunity to be part of a driven and ambitious team. Here, you can help shape the future of steel production while growing your own career in a company that values inclusion, collaboration, and personal development. We believe our success starts with our people – and together, we’re building a greener tomorrow. A permanent position in one of Sweden’s most exciting industrial projects. Competitive salary and benefits package in line with Union-negotiated agreements. 25 days of annual leave, in accordance with Swedish labor standards. Full relocation support, including housing assistance, travel arrangements, and relocation compensation. Visa sponsorship where applicable. Modern, purpose-built facilities in Boden with a focus on safety, sustainability, and innovation. A supportive and inclusive work environment where everyone is encouraged to grow and thrive. Working in Boden Our Boden site is right in the heart of a growing green industrial hub in Northern Sweden. It’s where we’re building one of the world’s most modern, sustainable steel plants. With just a 10-minute commute from town, you'll be close to both cutting-edge technology and the everyday convenience of community life. Your application Studies show that women and underrepresented groups often hesitate to apply unless they meet every requirement. At Stegra, we’re building an impact-driven, sustainable company - and we need a diverse, inclusive team to make it happen. If you share our passion but don’t meet every qualification, we encourage you to apply anyway. You might be the perfect fit for this role, or another as we grow. About Stegra Stegra is on a mission to change the global steel industry by producing green hydrogen, iron, and steel - with the goal of eliminating CO₂ emissions. Instead of coal, we use green hydrogen and fossil-free electricity, meaning our primary emissions will be water and heat. By 2030, our ambition is to produce 5 million tonnes of green steel annually in our fully integrated, digitized, and sustainable plant in Boden, Northern Sweden - currently under construction. But this is just the beginning. Our expertise in green hydrogen will enable us to decarbonize industries beyond steel, paving the way for a cleaner future. If you encounter any challenges when you are sending your application, please contact us on BlueCollarHiring@stegra.com and we will be happy to help.
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