The Mission: The Product Architect & Quality Diplomat
Are you the kind of person who can translate complex technical jargon into "Compliance-speak" for a customer, while simultaneously ensuring a batch record is airtight?
Our Randstad client in Visp is looking for a QA Product Quality Stewards to join their Quality Leadership Team. In this role, you aren’t just a reviewer; you are the technical bridge between the client’s vision and regulatory reality. You’ll be the "Go-To" guru for customer projects, ensuring that every product lifecycle is as robust as it is compliant.
Your Main Acts
The Technical Liaison & SME
You are the face of Quality for our customers. You don’t just answer questions; you provide the technical backbone for every project decision.
* The Voice of Quality: Act as the primary technical QA contact for customers, handling inquiries and providing expert input that keeps projects moving.
* Audit Frontman: When health authorities or customers come knocking, you’re the Subject Matter Expert (SME) in the room, defending the technical integrity of the product.
* Agreement Architect: You’ll execute and manage Quality Agreements, ensuring expectations are set in stone (and GMP-compliant).
The Product Guardian
You oversee the product’s journey from method transfer to final release, ensuring no technical detail is left to chance.
* Document Master: You’ll generate and approve the "heavy hitters": Master Batch Records, defect libraries, sampling plans, and product-specific SOPs.
* The Release Coordinator: You own the timeline. You coordinate the batch manufacturing and QC release activities to ensure the product hits the market on time and in perfect health.
* Validation Virtuoso: Support method transfers and validation activities, ensuring technical robustness is baked into the process from day one.
The Regulatory Translator
Working closely with Regulatory Experts, you’ll provide the technical DNA for regulatory submissions, ensuring that what we do on the shop floor translates perfectly to what we tell the authorities.
Your Backstory
* The Academic Foundation: You hold a degree in Biochemistry, Biotechnology, Pharmacy, or a related technical field.
* The GMP Native: You have at least 5 years of hands‑on experience in technical QA. If you’ve worked in sterile production, you’re already at the top of our list.
* The Bilingual Professional: You are fluent in German and English. You can navigate a technical debate in both languages without breaking a sweat.
* The Technical Mix: You have a proactive mindset and a genuine love for Quality Control and Microbiology.
* The Independent Collaborator: You’re a self‑starter who can work solo on a complex specification but knows exactly when to pull in the cross‑functional team to cross the finish line.
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