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Process Validation Engineer - Biotech Manufacturing (Contract)
Location: Neuchatel, Switzerland
Contract Position | Languages: English & French
Initially till 31.12.25, extension possible
Are you passionate about cutting-edge biotech manufacturing? Join a leading pharmaceutical team as a Process Validation Engineer, where you'll play a key role in ensuring successful validation of Drug Product (DP) manufacturing processes. This is your chance to work in a dynamic, collaborative environment focused on high-quality, compliant production of recombinant proteins.
What You'll Do:
* Develop & Standardize Protocols: Create engineering and PPQ (Process Performance Qualification) run protocols aligned with GMP and regulatory standards.
* Support Execution: Partner closely with Manufacturing teams to ensure flawless execution of validation runs, troubleshooting as needed.
* Document & Report: Draft and finalize detailed validation reports, incorporating data, deviations, and technical observations.
* Collaborate Cross-Functionally: Work with QA, Process Engineering, and other departments to align validation work with project goals.
* Drive Improvement: Apply best practices and new technologies to continuously enhance validation processes.
What We're Looking For:
* 3-5 years' experience in process validation for recombinant proteins.
* Degree in Biotechnology, Engineering, or a related field.
* Fluency in English and French.
* Proficient in Kneat software for validation documentation.
* In-depth understanding of GMP, Process Validation, PPQ, and risk management.
* Strong technical writing and documentation skills.
* Effective team collaborator with a proactive, problem-solving mindset.
Why Apply?
* Join a respected organization in the pharmaceutical/biotech sector.
* Contribute to impactful validation projects.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Management and Manufacturing
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