Job details
On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects.
Location: Neuchâtel, Switzerland
Contract Duration: 07/04/2025 – 31/05/2025 (Temporary contract via Randstad, with possible extension)
Work Mode: 100% Onsite
Position: QA Validation Expert
On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects.
Main Responsibilities:
* Review of Validation Protocols
* Assess protocols related to equipment, processes, CIP, SIP, computerized systems, and HVAC/Utilities
* Ensure alignment with GMP standards, internal quality procedures, and international regulations (FDA, EMA, etc.)
* Validation Report Review
* Evaluate test results to confirm all protocol requirements are met
* Identify deviations and propose appropriate corrective actions
* Quality Support
* Collaborate with cross-functional teams (Production, Engineering, Validation) to ensure quality integration
* Provide quality input during project meetings
Required Profile:
* Education:
* Degree in Pharmacy, Biotechnology, Chemistry, or another scientific discipline
* Experience:
* Minimum 2 years in a similar role within the pharmaceutical industry
* Hands-on experience in validation of process, equipment, CIP/SIP, computerized systems
* Experience with filling lines and freeze-dryers is a strong asset
* Technical Skills:
* Solid knowledge of GMP and regulatory guidelines (FDA, EMA, ICH)
* Familiarity with IQ/OQ/PQ protocols and risk assessment methodologies
* Soft Skills:
* Excellent attention to detail and strong analytical skills
* Effective communicator, able to interact with cross-functional stakeholders
* Solution-oriented mindset with the ability to manage several priorities under pressure
* Fluency in English and French is a strong advantage
What’s in it for you:
- Contribute to high-impact validation projects in a reputable pharmaceutical company
- Gain valuable experience in GMP and regulatory-driven environments
share this job.
Luciana Sardo
- +41 58 201 55 55
- Basel Professionals Life Sciences