> Markdown version of [/jobs/ext/4677531-life-sciences-biopharma-specialist-open-application](https://www.wearedevelopers.com/jobs/ext/4677531-life-sciences-biopharma-specialist-open-application). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # life sciences | biopharma specialist | open application. - **Company:** Randstad - **Location:** DIEMEN, Netherlands - **Salary:** €5,000 - **Contract:** Permanent contract - **Skills:** Data Analysis, Failure Mode Effects Analysis, Laboratory Information Management Systems, GXP - **Published:** November 12, 2026 - **Apply:** https://www.yacht.nl/vacatures/9218424/sollicitatie ## About the Role To be successful in these roles, you should have the following professional hard skills: + Bachelor's or Master's in Biotechnology, Pharma, Biomedical Engineering, or Chemistry + Proven work experience in a laboratory and industrial setting within the Pharmaceutical, Biotech, Medical Devices, Biomedical Engineering, or Chemistry sectors. + Experience with relevant regulations, such as GMP, GLP, ISO, FMEA, FDA + Strong verbal and written communication skills in English and Dutch (desirable) * ## Description Depending on the specific client assignment and your area of expertise, your core responsibilities may include: * Research & Development: Designing and conducting experimental studies, analyzing data, and contributing to the development of next-generation products, assays, and processes. * Quality Assurance & Quality Control (QA/QC): Ensuring laboratory and manufacturing operations adhere strictly to internal quality standards and international regulatory frameworks. * Process Optimization & Scale-Up: Evaluating and refining existing bioprocesses and manufacturing workflows to enhance yield, improve efficiency, and lower production costs. * Project Management & Execution: Managing project milestones from concept through execution, ensuring on-time delivery, cross-functional alignment, and regulatory compliance. Desired Skills & Experience We welcome applications from professionals with practical experience in one or more of the following areas: * Bioprocessing: Upstream Processing (USP), Downstream Processing (DSP), microbial fermentation, or mammalian cell culture. * Analytical & Molecular Biology Techniques: Chromatography (HPLC, FPLC), protein purification, ELISA, FACS/flow cytometry, Western Blot, qPCR, molecular cloning, or NGS/sequencing. * Quality & Regulatory Compliance: GMP, GLP, GxP standards, FDA regulations, and ISO standards (e.g., ISO 13485, ISO 14971, ISO 17025). * Validation & Continuous Improvement: Process Validation, New Product Introduction (NPI), FMEA, and Root Cause Analysis. * Data & Systems: Laboratory Information Management Systems (LIMS) and electronic lab notebooks (ELN)., Depending on the specific client assignment and your area of expertise, your core responsibilities may include: * Research & Development: Designing and conducting experimental studies, analyzing data, and contributing to the development of next-generation products, assays, and processes. * Quality Assurance & Quality Control (QA/QC): Ensuring laboratory and manufacturing operations adhere strictly to internal quality standards and international regulatory frameworks. * Process Optimization & Scale-Up: Evaluating and refining existing bioprocesses and manufacturing workflows to enhance yield, improve efficiency, and lower production costs. * Project Management & Execution: Managing project milestones from concept through execution, ensuring on-time delivery, cross-functional alignment, and regulatory compliance. ... Desired Skills & Experience We welcome applications from professionals with practical experience in one or more of the following areas: * Bioprocessing: Upstream Processing (USP), Downstream Processing (DSP), microbial fermentation, or mammalian cell culture. * Analytical & Molecular Biology Techniques: Chromatography (HPLC, FPLC), protein purification, ELISA, FACS/flow cytometry, Western Blot, qPCR, molecular cloning, or NGS/sequencing. * Quality & Regulatory Compliance: GMP, GLP, GxP standards, FDA regulations, and ISO standards (e.g., ISO 13485, ISO 14971, ISO 17025). * Validation & Continuous Improvement: Process Validation, New Product Introduction (NPI), FMEA, and Root Cause Analysis. * Data & Systems: Laboratory Information Management Systems (LIMS) and electronic lab notebooks (ELN).