Sökresultat för "Contamination Control"

SallyQ AB

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger. About the Role You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements. Key Responsibilities Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes. Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance. Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices. Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes. Design and evaluate smoke studies to verify airflow performance and first-air protection. Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies. The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week. Your Profile You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind. Qualifications Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment. Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations. Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing. Proven track record leading deviation investigations, root cause analyses, and CAPA implementation. Excellent analytical, problem-solving, and technical writing skills. Strong stakeholder management and collaboration across multiple functions. Ability to independently manage complex projects and drive continuous improvement initiatives. Application If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application. About Galderma Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

SallyQ AB

The role We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site. You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation. Key Responsibilities Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards. Oversee environmental monitoring, cleanroom qualification, and aseptic practices. Review sterilization validations and lead media fill programs. Drive contamination risk assessments, investigations, and CAPAs. Act as SME during audits and inspections. Provide training and mentorship in sterility assurance best practices. The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week. Your Profile You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift. You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it. Requirements Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline. 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry. Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits. Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations. Skills Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control. Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems. Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S). Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies. Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives. Excellent documentation skills and a structured approach to problem-solving and investigations. Strong communication and collaboration skills with the ability to influence cross-functional teams. Application If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application. About Galderma Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

APR Technologies AB

APR Technologies is a Swedish deep tech company developing high-performance liquid cooling solutions for data centers, space, defense, telecom, and battery applications. Our core technology Rheion™, co-developed with NASA, ESA, and Airbus, controls and redirects cooling liquid flow at chip scale, removing thermal barriers to technological progress while saving energy and enabling higher compute density. We are now looking for a Fluid & Coolant Specialist to join our R&D team in Enköping, Sweden. The role In this role you will design and test fluid handling systems and components, focusing on thermal performance, flow, pressure, and materials compatibility. Key responsibilities: • Evaluate and select fluids/coolants based on thermal, hydraulic, electrical, chemical, environmental, and reliability requirements. • Continuously monitor the market for existing and emerging coolant technologies. • Characterize and assess fluid properties including viscosity, density, thermal conductivity, specific heat capacity, dielectric strength, vapor pressure, and electrical conductivity. • Define qualification methodologies and perform verification testing of new fluids. • Define and execute material compatibility testing with metals, polymers, elastomers, adhesives, coatings, and electronic materials. • Investigate coolant ageing, contamination, corrosion mechanisms, and degradation effects throughout product lifetime. • Define and perform electrohydrodynamic pumping performance testing for new fluids. • Support mechanical and electrical engineering teams in material selection and fluid-related design decisions. • Maintain and continuously develop a database of fluid properties, compatibility data, and test results. • Assess environmental, health, safety, and regulatory aspects of coolant candidates, including sustainability and recyclability considerations. • Participate in design reviews and contribute to engineering decisions related to cooling technologies, fluid selection, and system reliability. • Collaborate across engineering disciplines to ensure integrated product performance. Required qualifications: • Degree in Chemical Engineering, Thermal Engineering, Chemistry, Materials Engineering, or equivalent. • Knowledge of coolant chemistry, electrochemistry, thermophysical fluid properties, and material compatibility. • Understanding of liquid cooling systems, and heat transfer relevant parameters. • Experience in experimental testing and data analysis. • Strong analytical, communication, and documentation skills. • Fluent in English. Meriting qualifications: • Experience with dielectric fluids, liquid cooling, or molecular pumping technologies. • Experience in coolant qualifications, reliability testing, or material compatibility assessments. • Hands-on experience with pumps, flow systems, and instrumentation. Application Send your CV and cover letter to careers@aprtec.com by 31 July 2026.

Blykalla AB

Blykalla is scaling rapidly to industrialize our next-generation small modular reactor (SMR) technology. If you are passionate about nuclear technology and want to make a real impact on the future of clean energy, we’d love to hear from you. Do you thrive on solving complex chemical and material challenges through hands-on experimentation and analytical thinking? We are looking for a Nuclear Waste Chemist - an experimentalist role to help develop Blykalla’s backend chemistry and waste management strategies for our lead-cooled SMR technology. In this role, you will combine experimental R&D, technical analysis, and cross-functional collaboration to support areas such as waste minimization, coolant purification, material reuse, spent nuclear fuel (SNF) handling and backend system development. This is an opportunity to help build both the technical foundations and laboratory capabilities for one of Europe’s most advanced nuclear startups. What we do at Blykalla Blykalla is developing the next generation of nuclear technology through advanced Small Modular Reactors (SMRs) based on innovative fuel, materials, and reactor designs. As Sweden’s leading SMR developer, our mission is to decarbonize industry and provide safe, scalable, and sustainable energy solutions. Our reactors use uranium nitride fuel and lead coolant, creating unique opportunities and challenges across fuel cycle chemistry, coolant purification, and waste management. What You'll Do You will play a key role in building Blykalla’s experimental capabilities related to backend systems and nuclear waste management. Your responsibilities include: Help establish and develop Blykalla’s in-house chemistry laboratory and experimental capabilities. Design, plan, and perform experiments related to waste treatment, coolant purification, and material handling. Troubleshoot experimental systems, identify suitable analytical methods, and independently drive investigations forward. Contribute to technical reports, feasibility studies, licensing documentation, and strategic decision-making. Investigate opportunities to reduce low-, intermediate-, and high-level waste volumes through purification strategies, system design, and material choices. Analyze and evaluate expected waste streams, both solid and liquid, based on reactor operating conditions and system design. Evaluate treatment, purification, recycling, and waste management methods for Pb coolant, activated materials, and SNF, including contamination control and backend management considerations. Work closely with national laboratories, industrial partners, and regulators to turn research into deployable solutions. Act as an internal technical resource for chemistry-related questions across the waste lifecycle and backend systems. Who You Are You are analytical, hands-on, and motivated by solving difficult technical problems. You enjoy experimental work and are comfortable navigating uncertainty in a fast-moving R&D environment. You are someone who can combine theory with practical execution — designing experiments, troubleshooting equipment and processes, analyzing data, and communicating results clearly. Even when facing unfamiliar systems or analytical methods, you know how to identify the right tools, techniques, and collaborators to move forward. You work well across disciplines, communicate effectively, and enjoy building new capabilities from the ground up. Above all, you want to contribute to meaningful long-term solutions in clean energy and nuclear technology. We Believe You Have MSc or PhD in chemistry, radiochemistry, chemical engineering, materials science, or a related field For MSc candidates: approximately 2+ years of relevant industry or research experience Hands-on chemical wet lab experience, including designing and executing experimental setups and evaluating chemical processes Strong analytical skills, with the ability to structure, interpret, and present complex data clearly Strong technical writing and communication skills Experience collaborating with research facilities, laboratories, industrial partners, or technical vendors Fluent in English, written and spoken The Following is Considered a Big Plus Knowledge of lead chemistry, fuel chemistry, actinide behavior, or fission product separation Experience with radioactive or hazardous waste systems Familiarity with coolant purification or backend fuel cycle systems Experience with waste classification frameworks or nuclear waste management strategies Experience writing technical reports for licensing, feasibility studies, or regulatory applications Experience with programming, scripting, or modeling for scientific and technical applications Location The position is based in Stockholm, Sweden, with occasional travel to partner laboratories and industrial sites. So, What Do You Think? Join us in transforming nuclear energy and building a more sustainable future. At Blykalla, you’ll work alongside ambitious engineers and scientists solving some of the most important energy challenges of our time — developing safe, clean, and reliable power systems for the future. We are proud to foster an inclusive workplace free from discrimination. We believe diversity of experience, perspectives, and backgrounds creates stronger teams, better technology, and a better workplace for everyone. We encourage applicants from all backgrounds to apply.

Silex Microsystems AB

Silex is investing strategically in MEMS testing as a core capability to strengthen our position in the market and deliver industry-leading solutions to our customers. As part of this effort, we are expanding our MEMS test infrastructure, methodologies, and expertise. This is a unique opportunity to be part of a forward-looking initiative that will define the next generation of MEMS performance and reliability. Read more about Silex here. About the role We are looking for a professional with a strong focus on test engineering and hands-on experience with test equipment and measurements, and related software development. You will join a growing and collaborative engineering team dedicated to developing advanced test solutions that support the full product lifecycle – from early prototypes to high-volume manufacturing. As a MEMS Test Engineer, you will play a key role in developing, optimizing, and executing test systems – both hardware and software – for a broad range of MEMS products, ensuring performance meets customer specifications and industry standards. You will collaborate cross-functionally within Silex and communicate with both suppliers and customers. In this role you will: Design and implement test solutions based on MEMS device specifications, covering electrical, optical, and mechanical performance. Develop and validate test cases and procedures for both manual and automated wafer-level and die-level test systems. Select, configure, and maintain specialized test instrumentation, including probe stations, precision source-measure units (SMUs), oscilloscopes, and custom MEMS test fixtures. Perform hands-on testing in both cleanroom and laboratory environments, ensuring proper handling of sensitive MEMS devices and adherence to ESD and contamination-control procedures. Analyze and interpret test data to evaluate device performance, identify trends, and diagnose issues at both the device and system level. Collaborate closely with design, process, and product engineers to troubleshoot, optimize test coverage, and improve product yield and reliability. Thoroughly document all test plans, configurations, and results to ensure full traceability and enable continuous improvement in test methods and equipment. Drive improvements in throughput, automation, and measurement accuracy across the MEMS test process flow. Ensure all activities comply with quality standards, customer requirements, and relevant industry regulations. We are looking for someone who has A Masters degree or Ph.D. in Engineering, preferably in Electrical Engineering, Engineering Physics, or a related field. At least 3 years of experience in electrical measurements, device characterization, or production tests – ideally including MEMS or semiconductor tests within an industrial environment or academia. Experience in LabVIEW programming for test automation, instrument control, and data acquisition. Proficiency in Python and familiarity with SQL databases for data analysis, visualization and structured data management. Hands-on experience with a wide range of test equipment, such as source-measure units (SMUs), parametric analyzers, probe stations, oscilloscopes, spectrum analyzers, and other specialized tools used in MEMS testing. Experience in cleanroom or controlled laboratory environments. Strong analytical mindset and problem-solving skills, with the ability to troubleshoot complex device- and system-level issues. Basic knowledge or experience in 3D CAD modeling and prototype manufacturing methods (e.g., 3D printing, CNC machining) for test fixture design and development. What we offer you Collaboration with a team of exceptional colleagues who share your passion for technology. Opportunities to work with cutting-edge MEMS technology in a state-of-the-art environment. Being part of a world-leading company that drives innovation and shapes the future of MEMS development. Continuous knowledge sharing with global experts in MEMS process integration and development. About Silex Silex is the world’s largest and most advanced pure-play MEMS foundry, headquartered in Stockholm. MEMS is present in nearly all modern technology, from personal gadgets to automotive electronics, medical monitoring and testing equipment, and thermal management systems. With a team of expert engineers, operators, technicians, support staff, specialists, and more, Silex brings the ideas and concepts of the industry’s leading MEMS innovators to life. The Silex team brings together talented, curious, visionary, and determined individuals to break new ground in the industry alongside customers, developing the latest process technology within MEMS for global applications. As part of this team, you will work with some of the world’s largest technology giants and innovation leaders in industries such as medicine, life sciences, consumer electronics, telecommunications, automotive, and industrial sectors. The recruitment process We have an ongoing recruitment process and therefore encourage you to submit your application as soon as possible. To apply, please attach your CV and answer a few questions. Our process is competency-based and includes a personality and logic test as well as reference checks. Additionally, we will conduct a background check and drug test prior to employment, and as an employer, we perform random alcohol and drug tests for all employees.

Mycronic AB (publ)

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/