Sökresultat för "pharmaceutical industry"

Vill du ha en central roll i att säkra leveranser till våra kunder och bidra till att livsviktiga läkemedel når patienter i tid? Har du ett starkt driv att arbeta i gränslandet mellan kund, produktion och Supply Chain – och trivs i en dynamisk och regulatoriskt styrd miljö? Hos PolyPeptide får du en roll där du bidrar till att säkerställa en stabil, effektiv och kundfokuserad leveranskedja. Vi söker dig som vill ta ett helhetsgrepp om våra kommersiella flöden – från efterfrågeplanering till leverans och uppföljning – och som motiveras av att koordinera komplexa processer, bygga relationer och driva förbättringar. Är du redo att ta nästa steg och påverka på riktigt? Varmt välkommen med din ansökan! Om rollen Som Commercial Supply Chain Manager har du ett övergripande ansvar för att leda och koordinera våra Supply Chain aktiviteter för kommersiella produkter genom hela produktlivscykeln – från efterfrågeplanering till leverans och intäktsredovisning. Du fungerar som huvudsaklig kontaktperson gentemot våra kunder i leveransrelaterade frågor och säkerställer att vi lever upp till våra åtaganden vad gäller leveransprecision, kvalitet och service. Rollen innebär ett nära samarbete med både interna och externa funktioner samt brygga mellan kvalitetsorganisationerna internt och hos kund. Du arbetar tvärfunktionellt och koordinerar aktiviteter mellan bland annat produktion, inköp, planering, kvalitet, logistik och försäljning, med målet att säkerställa en stabil och effektiv leveransprocess. Du rapporterar till Director Supply Chain. Dina huvudsakliga arbetsuppgifter I rollen som Commercial Supply Chain Manager kommer du att: Vara huvudkontakt för tilldelade kunder och säkerställa en välfungerande dialog kring leveranser och prognoser Ansvara för efterfrågeplanering för produkter, inklusive hantering av prognoser och ordrar över en längre tidshorisont Säkerställa korrekt orderhantering och leveransdatum i nära samarbete med säljorganisationen Driva och bidra i S&OP-processen genom att integrera kundprognoser och orderdata Koordinera Supply Chain aktiviteter tvärfunktionellt mellan produktion, kvalitet, inköp, logistik och andra relevanta funktioner Säkerställa att leveranser sker i tid och med rätt kvalitet, samt proaktivt hantera och eskalera avvikelser Planera och koordinera leveranser tillsammans med interna specialister Leda Supply Chain relaterade projekt kopplade till kommersiella produkter Säkerställa korrekt data i ERP-system och bidra till korrekt intäktsuppföljning Följa upp och rapportera KPI:er, såsom OTIF (On-Time In-Full), samt driva kontinuerliga förbättringar Vem är du? Kandidat- eller Masterutbildning inom Supply Chain, teknik, kemi eller motsvarande Tidigare arbetslivserfarenhet av Supply Chain projektledning i en CDMO verksamhet Tidigare erfarenhet av att arbeta inom läkemedel- eller medical device industrin enligt GMP God förståelse för hela supply chain-flödet (end-to-end) Erfarenhet av S&OP-processer och arbete i affärssystem (ERP) Mycket goda kunskaper i svenska och engelska, både i tal och skrift Vi söker dig som har en stark kundorientering och trivs i en roll med många kontaktytor. Du är strukturerad, analytisk och lösningsorienterad, med en god förmåga att driva och koordinera flera parallella aktiviteter. Du är en tydlig kommunikatör som kan skapa samsyn mellan olika funktioner, och trivs i en föränderlig miljö där du har förmågan att strukturera och prioritera komplexa arbetsuppgifter. Stämmer denna beskrivning in på dig? Sök då till oss! PolyPeptide erbjuder en attraktiv arbetsmiljö där både medarbetare och verksamheten får utrymme att utvecklas tillsammans. Gillar du att utmana dig själv och drivs av att kunna påverka saker till att bli bättre? Då hoppas vi att tjänsten intresserar dig och att du ansöker omgående, dock senast den 19 augusti 2026. Vi tillämpar löpande urval för tjänsten. På grund av semestertider kan återkopplingen dröja längre än normalt. För ytterligare information kontakta Theoharis Armutidis, Director Supply Chain, Theoharis.Armutidis@polypeptide.com. Om oss PolyPeptide Group AG och dess konsoliderade dotterbolag ("PolyPeptide") är en specialiserad kontraktstillverkare och utvecklingsorganisation (CDMO) för aktiva läkemedelssubstanser baserade på peptider och oligonukleotider. Genom att stödja våra kunder, främst inom läkemedels- och bioteknikindustrin, bidrar vi till hälsan hos miljontals patienter världen över. PolyPeptide verkar på en snabbt växande marknad och erbjuder produkter och tjänster från preklinisk fas till kommersiella stadier. Vår breda portfölj speglar möjligheterna inom läkemedelsterapier över olika områden, med stor exponering mot metabola sjukdomar, inklusive GLP-1. Med rötter tillbaka till 1952 driver PolyPeptide idag ett globalt nätverk av sex GMP-certifierade anläggningar i Europa, USA och Indien. PolyPeptides aktier (SIX: PPGN) är noterade på SIX Swiss Exchange. United by Purpose På PolyPeptide är vi stolta över att bidra till läkemedel som gör verklig skillnad för människors liv och hälsa. Hos oss blir du en del av ett arbete som betyder något, varje dag. Vi drivs av våra värdeord trust, innovation och excellence. Det märks i hur vi samarbetar, hur vi löser problem och hur vi tar ansvar för kvalitet och säkerhet för de patienter som i slutänden påverkas av vårt arbete. Vi är ett företag i snabb utveckling. Tillväxten innebär högt tempo, förändring och nya möjligheter för både medarbetare och verksamhet. Här växer du tillsammans med oss. Om du söker en arbetsplats där syfte, gemenskap och utveckling går hand i hand, då är PolyPeptide rätt plats.

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 an experienced Automation Engineer What You Will Work On Develop and configure automation solutions for pharmaceutical manufacturing systems Design and implement control logic, sequences, phases, and interlocks Configure and optimize DeltaV or equivalent DCS automation platforms Develop HMI screens and operator interface solutions Configure alarm management and control strategies Integrate process equipment with control systems and higher-level applications Support batch control and recipe implementation Participate in FAT, SAT, commissioning, and system verification activities Troubleshoot automation systems during testing and startup Prepare and maintain automation documentation and technical specifications Support qualification and Computerized System Validation (CSV) activities Collaborate with process, validation, commissioning, and engineering teams Ensure compliance with GMP, GxP, and pharmaceutical quality standards Support system improvements and automation optimization throughout the project lifecycle What You Bring Experience as an Automation Engineer within the pharmaceutical industry or another GMP/GxP-regulated environment Strong hands-on experience with DeltaV or similar DCS/process automation platforms Experience configuring control logic, sequences, phases, interlocks, and alarm functions Experience developing HMI applications and operator interfaces Experience integrating process equipment with automation and supervisory systems Good understanding of GMP, GxP, and Computerized System Validation (CSV) Experience performing FAT, SAT, commissioning, startup, and automation verification Experience troubleshooting, testing, and documenting automation solutions in regulated environments Ability to work effectively with process, validation, and commissioning teams Strong analytical, troubleshooting, and communication skills

Sobi är ett biofarmaceutiskt bolag med en kapabilitet och kunskap mellan allt från sen klinisk forskning, tillverkning och varuförsörjning av biologiska läkemedel till förmågan att möjliggöra tillgång och distribution av dessa behandlingar. Vi lägger vårt fokus där vi kan göra störst skillnad. Our client is an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. They work with a focus on providing better life quality for patients with rare diseases. You will be part of the Global Supply Chains Operations department and play a key role in making their products and medicines available to their patients. Send in your resume today, position start is September 2026. Information about the position Professionals Nord is, on behalf of our client, looking for a Coordinator. You will work as a consultant through our staffing business until August 2027. Work tasks Customer Order administration, order taking, batch reservation, pick and pack ordering, shipment booking and monitoring, invoicing, crediting, returns and customer qualification Month-end financial reporting in terms of Stock and Sales Responsible for monotoring interface transactions between HQ and affiliates Serial Number alerts management (if applicable) Process Continues Improvement (if applicable) We are looking for You who has a education from university with focus on supply chain, logistics, export administration and/ or economics Fluent in English, both orally and in writing Very good computer skills It is meritorious if you Have knowledge in Swedish, both orally and in writing Experience from the pharmaceutical Industry   In this recruitment process we put big focus on your personal characteristics. To succeed in the role we see that you are: Structured Analytical A fast learner Have a business mindset START: 1 September 2026 COVERAGE: Full-time CITY: Stockholm, Norra stationsgatan  SELECTION: Ongoing Apply for the position by clicking on "apply for the job/sök jobbet" below. We work with the process continuously and may proceed with candidates before the ad is removed. If you want, you can also create a user and upload your CV and cover letter. We do unfortunately not accept applications by mail, but if you have questions about the position, you are welcome to contact us at filippa.furugren@pn.se

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 an experienced Validation Lead What You Will Work On Define and lead the overall validation strategy for the project Develop verification and qualification approaches for technical systems and equipment Lead validation activities across project phases Perform and coordinate risk assessments related to validation Ensure full compliance with GMP and GxP regulations Lead Computerized System Validation (CSV) activities Validate computerized systems, manufacturing processes, and technical equipment Support validation of DeltaV or similar automation platforms Develop and maintain traceability matrices Coordinate qualification activities including IQ, OQ, and related verification processes Manage validation documentation and compliance deliverables Lead deviation investigations, CAPA activities, and corrective actions Collaborate with automation, process, commissioning, engineering, and quality teams Coordinate validation activities across multiple stakeholders Ensure successful delivery of validation objectives within project timelines What You Bring Several years of validation experience within the pharmaceutical industry Strong knowledge of GMP and GxP regulatory requirements Extensive experience with Computerized System Validation (CSV) Experience validating computerized systems, manufacturing processes, and technical equipment Practical experience with DeltaV or similar automation platforms in regulated environments Experience developing validation strategies and verification approaches Experience conducting risk assessments and qualification planning Experience with traceability matrices and requirements management Experience handling deviations, CAPA, and validation documentation Strong leadership, coordination, and stakeholder management skills Excellent communication and technical documentation skills

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 an experienced Commissioning Lead What You Will Work On Lead commissioning and installation activities throughout the project lifecycle Plan, coordinate, and execute commissioning activities for technical systems and equipment Manage the transition from installation to operational startup Coordinate activities across process, automation, validation, production, and installation teams Support commissioning of DeltaV or similar automation platforms Plan and execute FAT, SAT, functional testing, and integrated system testing Manage punch lists and commissioning close-out activities Conduct readiness reviews before startup and handover Coordinate system handover to operations and qualification teams Lead contractors and coordinate on-site commissioning activities Ensure compliance with GMP requirements and project quality standards Manage project schedules, risks, and commissioning deliverables Collaborate with cross-functional engineering and project teams Drive safe and efficient startup of manufacturing systems and facilities What You Bring Several years of experience leading commissioning or installation activities within the pharmaceutical industry Experience commissioning systems in GMP-regulated environments Strong experience coordinating process, automation, validation, production, and installation teams Hands-on experience with DeltaV or similar automation platforms Experience planning and executing FAT, SAT, functional testing, and integrated testing Experience managing punch lists, readiness reviews, and system handovers Experience leading contractors and coordinating site activities Strong understanding of project management, risk management, and scheduling Excellent stakeholder management and leadership skills Strong communication and technical documentation abilities

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 an experienced Sub Project Manager What You Will Work On Lead the CIP and Isolator workstream during the project execution phase Manage sub-project activities from execution through project completion Coordinate suppliers, contractors, and internal project teams Drive technical discussions and resolve complex project challenges Ensure project delivery according to scope, schedule, budget, and quality objectives Develop and maintain project plans, resource plans, and timelines Manage project risks using a structured risk-based approach Drive risk identification, mitigation, and follow-up activities Monitor project progress and report status to project management Ensure compliance with GMP standards and project requirements Support project documentation and technical decision-making Collaborate closely with engineering, quality, validation, and production teams Ensure effective communication across all project stakeholders What You Bring Proven experience as a Project Manager or Sub Project Manager within the pharmaceutical industry Experience leading at least three GMP-regulated projects from initiation to completion Strong experience managing large and complex investment or engineering projects Experience managing suppliers and external partners Strong knowledge of: GMP regulations Pharmaceutical manufacturing environments Project execution methodologies Experience working with risk-based project management Strong budget, schedule, and resource management skills Excellent communication skills in both Swedish and English Ability to work primarily onsite during the execution phase

Academic Resource is searching for a Direct Sourcing Lead / Planner to Life Science company in Uppsala. The job is a fulltime consultancy assignment, for 6 months initially with opportunities for extension. Location in Uppsala. Start as soon as possible. Description of the role / job tasks: The Direct Sourcing Lead is accountable for strategic and operational sourcing execution with full ownership for assigned commodities and suppliers. • Lead the development and execution of sourcing strategies for assigned commodities and suppliers, delivering competitive advantage through supplier selection, development, consolidation, and performance optimization. • Manage the full procurement lifecycle, including RFQs, negotiations, contracting, and purchase execution for assigned category. • Maintain full accountability for buy execution, meeting deflation, cost reduction, and KPI targets. • Drive supplier performance, optimization, and continuous improvement. • Perform detailed cost and manufacturing process analysis to ensure highest quality at the lowest total cost of ownership. • Analyze and apply structured sourcing tools for risk and spend optimization to deliver and improve sourcing targets • Collaborate closely with key business stakeholders to identify, qualify, and onboard suppliers and to ensure sourced material and services meet the needs of the business. • Building deep relationships with Strategic Suppliers driving early supplier engagement into NPI/NPD process, and long-term partnership for wing-to-wing product lifecycle. • Driving improvements in sourcing processes including escalations due to delivery/quality issues, invoicing/payables issues, and database management • Monitor global markets and regulatory trends and developments, become a commodity expert for the assigned commodities and proactively adapting sourcing strategies to mitigate risk and ensure long term supply security. • Working with businesses and suppliers to manage and track implementation of supply agreements, communicating to Business General Managers and other senior staff, obtain sign-off for projects. Requirements for the role: • Bachelor’s degree in Chemistry, Chemical Engineering, Chemical Technology or Engineering, Materials Science, Mechanical Engineering, Industrial Engineering, Packaging Engineering or other technical discipline OR Bachelor’s degree plus 5+ years of experience in Strategic Sourcing / Direct Procurement OR 9+ years of experience in sourcing or procurement if no technical degree. • 8-9 years of experience in direct procurement, strategic sourcing, GMP, regulated chemical supply markets, regulatory requirements, and sourcing best practices. • Life Sciences, Biotech, or Pharmaceutical industry experience preferred. • Excellent negotiations skills and analytical skills with the ability to handle and develop supplier relationships • Ability to energize, develop and establish rapport at all levels within an organization • Shown ability to execute and deliver on commitments • Experience implementing a compliant supply chain, supply agreement execution experience • Strong business/financial acumen, proficient in leading and setting direction, including demonstrated ability to motivate, influence and inspire change globally and across all levels of the organization. • High level of analytical skills and experience in driving global tender processes • Willingness to travel domestically and internationally • Fluent in English, both spoken and written. • Experience with ERP systems (e.g., SAP, Oracle) and procurement analytics tools • Excellent skills in Excel and Powerpoint Nice if you also have: • Master’s degree in Management or Engineering (MBA, MS, MTech) • Procurement or Supply Chain certifications (e.g. CIPS, CPSM, PMP) • Swedish spoken and written. • Greenbelt certification preferred. Soft skills: • Self-motivated and able to work independently and within the team • Excellent negotiation, communication, and cross-functional collaboration skills About Academic Resource: Academic Resource is the recruitment and staffing company for academics with experience. We have extensive experience in Leasing, Recruitment and Interim Management in the service sector. Our business areas are Life Science, Economics & Finance, and HR. We operate in the service sector and mainly in Stockholm & Uppsala. As a consultant at Academic Resource you are offered: • Benefits such as occupational pension, health care allowance and parental pay. • An authorized staffing company, which means much greater security, as you are covered by the terms of the collective agreement for, for example, salary, insurance, pension and vacation. • A dedicated consultant manager who is available and keeps in constant contact with you and the client companies throughout your employment, who ensures that you enjoy and develop in your workplace! • Opportunity to develop through learning on the job as well as in varied roles at interesting client companies. Application: Selection and interviews will be ongoing. The position may be filled before the last day of application therefore we recommend that you apply as soon as possible. Submit your CV written in English. Mark your application with reference number: CSL0426 Do you have any questions? Do not hesitate to contact us by email at: rekrytering.lifescience@academicresource.se Please note that we do not accept applications via email. we take you further

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role you will get the opportunity to work with committed colleagues in a collaborative team. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the way we work with our outsourced manufacturing activities. We are looking for an experienced Senior Outsourcing Manager to join our Manufacturing Operations team. In this role, you will be responsible for driving outsourcing programs for injectable pharmaceutical products to Contract Manufacturing Organizations (CMOs), with a particular focus on late-stage development projects. As Senior Outsourcing Manager, you will serve as the primary interface between Camurus and external manufacturing partners. This is a true Project Management role where you will ensure successful project execution from technology transfer through start of commercial production. You will work closely with internal stakeholders and external partners to secure reliable, compliant, and efficient delivery of the project. You will report to the Director Manufacturing Operations. Main responsibility Among others, your responsibilities will include: · Develop and manage project plans, timelines, and milestones for technology transfer, process development, process validation, and manufacturing readiness activities together with CMO partners. · Drive day-to-day collaboration with CMOs and ensure agreed deliverables, timelines, and performance targets are achieved. · Lead operational meetings and steering committee meetings with external manufacturing partners. · Identify risks and issues proactively and drive mitigation and resolution activities together with internal and external stakeholders. · Coordinate and manage changes with CMOs, ensuring proper documentation, implementation, and alignment with project plans and contractual commitments. · Collaborate closely with internal Camurus functions such as Quality, R&D, Regulatory Affairs and Supply Chain to ensure successful project execution. · Ensure manufacturing activities are conducted in accordance with applicable GMP requirements and regulatory expectations. · Support continuous improvement initiatives related to outsourcing, external manufacturing operations, and CMO performance. Candidate profile We are looking for a professional with extensive experience from pharmaceutical manufacturing operations including outsourcing and CMO management. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline. You have a solid understanding of GMP-regulated manufacturing environments and a proven track record of managing outsourcing programs and external manufacturing partners within the pharmaceutical or biotech industry. Experience from late-stage development, technology transfer and commercial manufacturing is highly valued. Experience from injectable products and combination products is considered a strong merit. As a person, you are structured, collaborative, and communicative, with a proven ability to drive complex projects and build strong relationships across multiple stakeholders. You combine a proactive and results-oriented mindset with a pragmatic and hands-on approach, while maintaining a humble and low-prestige attitude. Fluency in spoken and written and English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

Join CTC - where ambition is high and one of the goals is to strengthen the Swedish infrastructure in the Life Sciences! We are growing and are now looking for an additional Medical Writer who wants to contribute to CTC’s continued journey. Are you an experienced Medical Writer (MW) who wants to use your expertise to drive CTC’s development? Then this is the opportunity for you! As a Medical Writer at CTC, you will be part of a team of four other MWs responsible for writing and quality-checking regulatory documents, primarily clinical study protocols and reports. The work alternates between individual tasks and teamwork. You will be part of various study-specific project teams responsible for initiating and managing clinical projects until the delivery of study results. These cross-functional project teams include professionals such as project managers, medical and scientific advisors, research nurses, doctors, statisticians, and more. Main responsibilities: To write clinical study protocols and clinical study reports in accordance with ICH E6, ICH E3, and/or ISO 14155, and coordinate the development and quality control processes of these documents, both internally and with our clients. To write other regulatory documents and texts such as summary of results, narratives, substantial amendments and responses to authorities. To coordinate and lead meetings, both internally and externally, and act as a point of contact for clients. To serve as a mentor to colleagues. Other tasks such as medical coding, writing abstracts and scientific articles, writing assignments related to safety reporting, and writing marketing documents may also be required. We are looking for a driven and experienced Medical Writer who truly enjoys writing and formulating scientific texts. To succeed in this role, you need to have the ability to quickly and efficiently interpret, summarize, and present large amounts of data. We require you to have at least 3 years of experience in medical writing, drug development, and clinical trials. Previous experience in consultancy work and an understanding of the customer perspective are also valued. As a person, you are communicative and enjoy collaborating with experts in various fields. You are flexible, works independently, and deliver within agreed timelines. CTC’s core values: Innovation, Community, Respect, Commitment, and Professionalism resonate with you. Required qualifications MSc in the life sciences field. At least 3 years of experience in medical writing, drug development, and clinical trials. Experience in leading meetings and coordinating complex and parallel deliveries within agreed timelines. Proficiency in using the Microsoft Office suite, especially Microsoft Word. Excellent ability to express yourself grammatically correctly and clearly in English, both spoken and written. Good knowledge of the Swedish language (spoken and written). Preferred qualifications A PhD in the life sciences field. Experience with Phase 2-3 trials. Experience with medical devices and/or advanced therapy medicinal products (ATMP), as well as knowledge of regulatory requirements related to these areas. Experience in writing eCTD module 2; Clinical and Non-Clinical overview/summary, Investigator’s Brochures (IBs), Annual Safety Reports (ASRs). At CTC, you will be covered by a collective agreement and offered benefits such as flexible working hours, wellness allowance, and generous vacation terms. You will have the opportunity to work in a knowledge-intensive environment in a company with short decision-making paths, with good professional development opportunities. The position is located at our office in Uppsala (hybrid work is possible). Full time (40 hours per week). If you have questions, contact Marit Wangheim (Director Medical Writing) marit.wangheim@ctc-ab.se Please submit your application no later than 17 August 2026. CTC Clinical Trial Consultants AB is a Clinical Research Organization (CRO) with operations in Uppsala, Stockholm, Linköping, and Gothenburg. As a CRO, we conduct clinical trials and investigations on behalf of the pharmaceutical and medtech industry and academic institutions. We offer a comprehensive full-service solution that includes all the services, activities, and deliverables required to successfully conduct a clinical trial— bringing new pharmaceuticals and products to patients. We currently conduct clinical studies across all phases of development, from Phase 0 through Phase IV. Most of our studies are carried out at our own research clinics, although we also collaborate with external clinical sites. We employ approximately 125 people, around half of whom work in clinical roles. Our headquarters are located in Uppsala.

SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues. Job Overview The Sr Quality Engineer is responsible for acting as Workstream Lead Quality (QE Lead) in the Design & Development projects as responsible for design assurance activities across all project phases ensuring quality and robustness of the product design and manufacturing processes (including product care projects, design changes and design reviews). Furthermore, the Quality representative is responsible to assure compliance with applicable regulations and SHL Medical AB’s Quality Management System (QMS) in both Design & Development Projects and other Quality element tasks such as CAPAs and Change Control handling. Main Responsibilities Maintain and calibrate laboratory equipment and instruments to ensure operational reliability and compliance. To act as Workstream Lead Quality applying Quality Engineering principles in a dynamic way in development and production projects. To represent Workstream Lead Quality in all Design Controls and Product Development related aspects. To ensure that all design control and production/process control projects meet applicable (local and international) regulations, Corporate, Customer, and Local QMS requirements. To utilize Quality Engineering best practices, ensuring internal and external customers’ needs and requirements are built into new products and future product changes. To support SMEs in the identification and traceability of Critical to Quality attributes by applying Advanced Product Quality Planning/DFSS/Risk tools and techniques across all product development phases. To promote the use of statistics in testing and control of quality. To support and guide Risk Management activities (FMEAs). To assess and approve the risk mitigation techniques implemented and whether these are consistent with the product classification, potential defect types, defect frequency, severity, patient risk, process capability, product and process controls. To support Device product/process development and production activities, including the following: Develop or review product/process specifications and requirements. Develop or review product reliability specifications/predictions, and reliability test activities. To develop quality plans and work further with Manufacturing on the transfer of quality requirements. To contribute to compilation and maintenance of Design History Files (DHF). Minimum requirements Minimum 5+ years' work experience in relevant roles such as Quality Assurance, Quality Engineering Fluent in written and spoken English. Experience from working with interpretation of ISO Standards, e.g EN ISO 14971:2019 and EN ISO 13485:2016 Experience in establishing, reviewing and approving quality documentation Experience with model development, test method validation and statistical analysis. Green Belt practitioner, or demonstrated experience in application of Quality Methodologies such as DFSS, DMAIC, Lean Hands-on experience in product development from ideation to launch in the Medical Device Industry Preferred Qualifications Fluent in written and spoken Swedish. Experience with Design Controls and Design Transfer activities within the Medical Device industry Experience with injection molding and automated assembly manufacturing processes. Familiarity with validation activities including IQ/OQ/PQ and Test Method Validation (TMV). Experience working in cross-functional and international environments. We Offer Challenging assignments in a fast-growing and innovative industry. An exciting opportunity in a fast-growing international medical technology company. A modern working environment with multicultural and dynamic teams. A centrally located office in Zug, very close to the train station. Interested in joining SHL Medical and in supporting us with your expertise and personality? Then we look forward to receiving your application to our Talent Acquisition Department. Please note: We do not accept applications from recruitment agencies for this position

We're looking for a Junior R&D Lab Engineer to join our forward-thinking, dynamic team and help us create game-changing sensor systems for the biopharmaceutical industry. Do you want to be part of a growing company that's shaping new possibilities in the field? Come join us at ArgusEye — a growing company of around 15 people — and be part of our journey! About the role: You'll be part of a small but growing R&D team of six people dedicated to our sensor development. Your primary focus will be the development of new sensor chips and to test new hardware, a role where your ideas and skills will directly influence the future of our technology. This means planning, designing, and executing experiments related to sensor development and characterization, as well as improving existing solutions. You'll get hands-on with manufacturing processes and surface chemistry, using techniques such as HPLC and other analytical methodologies to evaluate sensor performance. You’ll contribute not only to the development of our technology, but also to shaping how we work, build collaborations, and drive our future growth. What you'll do with assistance: Plan, design, and execute experiments related to the development and characterization of new sensor chips. Generate high-quality data to support the development of better data models. Contribute with ideas and concepts for sensor chip design and fabrication. Develop and validate new product prototypes for various applications. Maintain laboratory notebooks and electronic records in line with data quality and integrity standards. Prepare scientific reports, protocols, and presentations for internal and external stakeholders. Perform regular lab maintenance to ensure a clean and safe work environment. Collaborate closely with other team members to successfully integrate sensor chips into our systems. We’re looking for someone who.. ..loves lab work and believes that great technology starts with curiosity and experimentation. You thrive in a collaborative environment and want to be part of a team where innovation happens every day, and where you can help shape both technology and company culture. About you: Hands-on lab experience, including chemical handling, experiments, and use of standard lab equipment in a wet lab, gained through work experience or academic studies, is required Holds relevant Master’s degree in for example Material science, Biomolecular chemistry, or Bio- and Nanomaterials Strong understanding of organic reactions and surface chemistry applied to sensor development Passion for problem-solving, innovation, and scientific exploration Analytical skills and experience in surface characterization and performance evaluation is a plus Why join us? Work on cutting-edge technology with real-world applications. Be part of a supportive, dynamic team where your contributions are valued. Grow your career in an innovative, fast-paced industry. Learn from our customers and attend industry and R&D conferences to grow professionally. Enjoy the freedom to take ownership of your work, supported by a flexible and relaxed environment that values responsibility. Experience a family-like atmosphere filled with collaboration, curiosity, and team activities like music quizzes, bowling and Friday fika. About ArgusEye: ArgusEye is on a mission to revolutionize biopharmaceutical production. Today, developing life-saving medicines is often a slow, complex, and expensive process, putting vital treatments out of reach for many. By providing advanced sensor systems for real-time monitoring of biological processes, we aim to change that. Our technology, built on 40+ years of research at Linköping University, combines nanoplasmonic sensing with fiber optics to deliver real-time data, speeding up medicine development, improving efficiency, and cutting costs. With partnerships among leading pharmaceutical companies and growing demand, we're scaling to make a bigger impact. At ArgusEye, you'll be part of a close-knit team where your ideas and contributions are truly valued. Together, we're making cutting-edge technology accessible to improve lives worldwide. START: Immediately LOCATION: Linköping JOB HOURS: Full-time CONTACT: Senior Recruiter Mikaela Ehk, mikaela.ehk@oddwork.se (contact for questions regarding the position, not applications) LAST APPLICATION DATE: Applications are reviewed on ongoing basis As a leading recruitment and employer branding company we challenge expectations and match talents with the right corporate culture while helping organizations create stronger employer brands. Curious and want to know more? Step into the world of Oddwork by clicking here or find more career opportunities here!

We're looking for a Product Developer to join our forward-thinking, dynamic team and support the development of game-changing sensor systems for the biopharmaceutical industry. Do you want to be part of a growing company of 15 that's shaping new possibilities in the field? Come join us at ArgusEye and be part of our journey! About the role: In this role, you'll design and develop advanced hardware devices that seamlessly integrate with our sensor chips, driving real impact in biopharma applications. From early idea generation to testing prototypes and final delivery, you'll take a leading role in planning, driving, and coordinating our hardware development projects. As part of our development team, you'll work across the entire product development process with a clear focus on project execution – setting direction, ensuring progress, and aligning stakeholders along the way. Your ability to combine hands-on engineering with strong project management skills will be key in bringing ideas to life and delivering reliable, high-performing products. What you'll do: Lead and drive hardware development projects from idea to finished product Solve engineering challenges and develop innovative solutions Design hardware using CAD tools Coordinate work with multidisciplinary teams and subcontractors Build prototypes, conduct tests, verify and validate designs Take an active role in shaping and improving how we run and manage hardware development projects We’re looking for someone who.. ..is driven by the opportunity to contribute to a life-critical industry through the development of advanced hardware solutions. With experience spanning the full development cycle, you’re used to taking ideas from concept to reality – planning, driving, and ensuring progress along the way. You bring a structured approach to development, where you naturally create clarity, keep momentum, and align people around a common goal to deliver high-quality results. About you: A Master's degree in Mechanical Engineering, Industrial Design, Physics, or a related field 3+ years of experience in product development Good knowledge and experience of GD&T (ISO GPS or ASME Y14.5) Skilled in CAD software (e.g., SolidWorks, or Autodesk Inventor) Proven ability to drive projects from A to Z, preferably in a regulated industry (biopharma, medtech, automotive or similar) A strong communicator who can collaborate with both technical and non-technical stakeholders Knowledge of optics, electronics, fluid mechanics, and simulation tools (e.g., COMSOL, ANSYS, Zemax) and quality systems like ISO 9001 or ISO 13485 is a bonus Why join us? Be part of a supportive, dynamic team where your contributions are valued Grow your career in an innovative, fast-paced industry Learn from our customers and attend industry and R&D conferences to grow professionally Enjoy the freedom to take ownership of your work, supported by a flexible and relaxed environment that values responsibility Experience a family-like atmosphere filled with collaboration, curiosity, and team activities like music quizzes, bowling and Friday fika About ArgusEye: ArgusEye is on a mission to revolutionize biopharmaceutical production. Today, developing life-saving medicines is often a slow, complex, and expensive process, putting vital treatments out of reach for many. By providing advanced sensor systems for real-time monitoring and control of bioprocesses, we aim to change that. Our technology, built on 40+ years of research at Linköping University, combines nanoplasmonic sensing with fiber optics to deliver real-time data, speeding up medicine development, improving efficiency, and cutting costs. With partnerships among leading pharmaceutical companies and growing demand, we're scaling to make a bigger impact. At ArgusEye, you'll be part of a close-knit team where your ideas and contributions are truly valued. Together, we're making cutting-edge technology accessible to improve lives worldwide. START: According to agreement LOCATION: Linköping JOB HOURS: Full-time CONTACT: Senior Recruiter Mikaela Ehk, mikaela.ehk@oddwork.se (contact for questions regarding the position, not applications) LAST APPLICATION DATE: Applications are reviewed on an ongoing basis As a leading recruitment and employer branding company we challenge expectations and match talents with the right corporate culture while helping organizations create stronger employer brands. Curious and want to know more? Step into the world of Oddwork by clicking here or find more career opportunities here!

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 an experienced Quality Manager IT What You Will Work On Ensure IT compliance for computerized systems and IT infrastructure Review and approve risk assessments, qualification, and validation documentation Review change controls, deviations, and periodic system reviews Ensure compliance with GMP, GxP, SOPs, and internal quality requirements Support Computerized System Validation (CSV) activities Participate in IT compliance, qualification, and validation projects Provide QA support for IT projects and system changes Ensure data integrity principles are applied across IT systems Maintain and update the inventory of computerized systems Collaborate with QA, IT, Validation, Infrastructure, and Business stakeholders Support continuous improvements in IT quality, security, availability, and compliance Contribute to regulatory inspections and audit readiness Review technical documentation to ensure regulatory compliance Support quality activities throughout the system lifecycle What You Bring Experience working in IT Compliance within the pharmaceutical, biotech, or other GxP-regulated industries Strong understanding of Computerized System Validation (CSV) Experience reviewing qualification and validation documentation Knowledge of GMP, GxP, and pharmaceutical quality systems Strong understanding of Data Integrity principles (ALCOA+) Experience with change control, risk assessments, and periodic reviews Experience supporting QA and validation activities for computerized systems Excellent communication and stakeholder management skills Pragmatic, solution-oriented, and collaborative mindset Flexible with a proactive approach to quality and compliance

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 an experienced Process Engineer What You Will Work On Translate process requirements into practical manufacturing solutions Develop process descriptions, process parameters, operating limits, and process documentation Support process development for GMP manufacturing operations Develop and optimize batch processes and recipe management Work with DeltaV or equivalent automation platforms Define process parameters, setpoints, and operating boundaries Support commissioning, process verification, testing, and startup activities Troubleshoot process and production issues Collaborate closely with automation, validation, and commissioning teams Support process safety through alarm philosophy and interlock design Ensure compliance with GMP/GxP standards and regulatory requirements Participate in process optimization and continuous improvement initiatives Prepare and maintain technical documentation throughout the project lifecycle What You Bring Experience as a Process Engineer within the pharmaceutical, biotech, or other GMP/GxP-regulated industries Strong understanding of batch manufacturing processes and recipe development Experience with DeltaV or similar Distributed Control Systems (DCS) Experience defining process parameters, setpoints, and operating limits Understanding of alarm philosophy, interlocks, and process safety principles Experience with process verification, testing, commissioning, and troubleshooting Experience collaborating with automation and validation teams Strong technical documentation skills Experience working in highly regulated manufacturing environments Good communication and collaboration skills

Cambrex Karlskoga är ett dynamiskt och växande företag inom läkemedelsindustrin, med spetskompetens inom avancerad organisk kemi. Vi utvecklar och optimerar kemiska processer för att tillverka aktiva läkemedelssubstanser (API) och intermediat som är avgörande komponenter i moderna läkemedel för att förbättra livskvaliteten världen över. Med cirka 500 medarbetare är vi en viktig del av den globala Cambrexkoncernen, som är verksam inom innovativ kemi och läkemedelsutveckling. Vår anläggning i Karlskoga kombinerar lokal expertis med internationell räckvidd, och vi är stolta över att bidra till en tryggare och friskare framtid. På Cambrex Karlskoga får du mer än bara ett jobb, du får en meningsfull karriär där du är med och gör verklig skillnad. Här bidrar du till utvecklingen av läkemedel som räddar liv och förbättrar människors hälsa världen över. Vi erbjuder en trygg och hållbar arbetsmiljö där kvalitet och säkerhet alltid står i fokus. Du får arbeta i en organisation som värdesätter långsiktighet, ansvar och ständig förbättring. Samtidigt blir du en del av ett engagerat och sammansvetsat team, där gemenskapen är stark och där vi tillsammans driver utvecklingen framåt, både lokalt och globalt! Om rollen Som automationsingenjör/programmerare hos oss får du en nyckelroll i att utveckla, optimera och säkerställa driftsäkerheten i våra styr- och övervakningssystem. Du arbetar i projektform tillsammans med projektledare, el & instrument, mekanik och driftorganisationen för att säkerställa att våra produktionsanläggningar fungerar stabilt, effektivt och i enlighet med GMP‑krav. Här får du möjlighet att arbeta både strategiskt och operativt – från design och utveckling till driftsättning och löpande förbättringsarbete. I rollen kommer du att: Programmera, konfigurera och underhålla ABB 800xA samt ABB AC450 Utveckla styrlogik, operatörsgränssnitt, sekvenser och larmhantering Delta i automations- och investeringsprojekt från designfas till driftsättning Arbeta med felsökning, incidenthantering och förbättringsåtgärder i produktionsmiljö Bidra till utveckling av interna standarder och arbetssätt Stödja driften vid förändringar, testning, FAT/SAT och kvalificering Delta i riskanalyser, Design Reviews och kontinuerliga förbättringsinitiativ Du rapporterar till Chef för Teknisk Service och rollen är placerad i Karlskoga. Vem är du? Du har en eftergymnasial teknisk utbildning inom automation, automatiserad tillverkning eller ett likvärdigt område, och erfarenhet av programmering och systemarbete i ABB 800xA och ABB AC450. Du har tidigare arbetat inom processindustri, kemisk industri eller annan reglerad miljö och har därigenom god förståelse för kravställning, dokumentation och kvalitetssäkrade processer. Det är dessutom meriterande om du har god förståelse för DCS‑arkitekturer, nätverkstopologier och industriella kommunikationsprotokoll, liksom erfarenhet av Siemens S7, Rockwell‑system eller SCADA‑plattformar såsom iFix eller Ignition. Kunskap om GMP är meriterande. Som person är du analytisk, noggrann och lösningsorienterad med förmåga att arbeta strukturerat i komplexa systemmiljöer. Du trivs med att samarbeta över teknikgränser och tycker om att arbeta nära produktion för att skapa långsiktiga och driftsäkra lösningar. I rollen behöver du kunna behärska det svenska språket i tal och skrift. Kontaktinformation Har du frågor om tjänsten är du välkommen att kontakta Chef för Teknisk Service Hasan Abdul Hussoon via mejl Hasan.Abdul.Hussoon@cambrex.com eller telefon 076-144 06 04 Fackliga kontaktpersoner: Tomas Hägerström, Akademikerföreningen, tfn 072-724 76 12 Jarno Koskinen, Unionen, tfn 073-054 68 02 Ansökan Välkommen in med din ansökan senast 2026-08-16. Urval sker löpande under ansökningstiden.

Are you an experienced TIG welder or mechanical assembler looking for an exciting career opportunity in Denmark? Join a Danish Engineering Company Building High-quality Food & Beverage Machinery Ferrum Group is a Danish engineering and manufacturing company that designs and builds high-quality processing and packaging machinery for the food and beverage industry. Due to continued growth and increasing demand, we are looking for 4-5 skilled professionals to join our team in Fredericia. Your Responsibilities Perform TIG welding of stainless-steel components and machine frames. Mechanical assembly of food and beverage processing equipment. Read and understand technical drawings. Install mechanical equipment. Ensure high-quality workmanship in accordance with food industry standards. Collaborate closely with engineers, technicians and project teams. What We're Looking For Vocational education a welder, metalworker, fitter or similar trade. Solid experience with TIG welding in stainless steel. Experience assembling industrial machinery or process equipment. Ability to read and understand mechanical drawings. Strong attention to quality and detail. Ability to work independently as well as in a team. Experience from the food, beverage, pharmaceutical or process industry is an advantage. Basic English communication skills are required. Danish language skills are not required. What We Offer Permanent full-time employment in a growing Danish company. Competitive salary based on your qualifications and experience. Modern production facilities with advanced manufacturing equipment. A safe, clean and well-organized working environment. Professional onboarding and supportive colleagues. Opportunities for personal and professional development. International projects and exposure to advanced engineering solutions. Relocation assistance for the right candidates. Ferrum can assist the right candidate with finding accommodation, CPR registration, etc. Gross salary range: 25 - 27 EUR/hour for skilled TIG welder/Mechanical assembly. Working schedule: In Ferrum we mainly work dayshift. Normally from 07.00 to 15.00 from Monday to Thursday, and from 07.00 to 13.00 on Friday. Other working schedule can be discussed. Location: Fredericia, Denmark Employment: Full-time | Permanent Positions Available: 4-5 Why Denmark? Denmark is consistently ranked among the world's best countries for work-life balance, safety and quality of life. Fredericia is centrally located with easy access to major cities, beautiful nature and excellent public services. About Ferrum Group Ferrum Group develops and manufactures advanced processing and packaging solutions for customers around the world. Our equipment is used in breweries, beverage production, food processing and industrial automation. Our headquarters and production facilities are located in Fredericia, Denmark, where quality, innovation and craftsmanship are at the heart of everything we do. Ready to Join Us? Send your application or contact us for more information: Email: info@ferrum-group.dk Website: www.ferrum-group.dk