Company Presentation
Akkodis is a global player in engineering and IT and a leader in smart industry. Present in 30 countries, our 50,000 experts combine technological expertise and sector knowledge to build a sustainable future, driven by a culture of inclusion and diversity.
Akkodis is the technology brand of The Adecco Group.
Job Information
Location: Bulle
Contract Type: Permanent
Work Authorization: Valid Swiss work permit, Swiss nationality, or EU citizenship required
For one of our leading clients in the biotech industry, we are seeking a Bioprocess Validation Specialist to support the final phase of tech transfer and execute critical process validation activities for biologics downstream manufacturing.
Mission (~80% validation execution / ~20% tech transfer support)
Write and prepare "Process Performance Qualification" protocols and reports
Execute and secure process validation phases for microbial biotechnological processes
Support tech transfer activities from development to commercial manufacturing
Coordinate sampling, analyses, and documentation in compliance with cGMP
Collaborate with development teams and QA stakeholders
Conduct risk assessments and ensure strict adherence to established processes
Support Health Authority inspections and regulatory documentation
Profile
Master's or Engineering degree in Biotechnology, Life Sciences, or related field
Proven experience in biotech industry in a similar validation/tech transfer role (mandatory)
Experience with PPQ protocol writing and process validation (highly desirable)
Tech transfer experience is a strong asset
Strong understanding of biotechnological manufacturing processes (downstream)
Knowledge of cGMP requirements and quality standards
Hands‑on experience with process validation and tech transfer activities
Ability to work with complex biotech manufacturing subjects
Bilingual French & English (written and verbal) - mandatory
Biotech industry exclusively (Pharma as second choice only)
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