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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
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
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