QA Validation Expert, Randstad

QA Validation Expert

Randstad

Location:
Switzerland, Neuchâtel

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Not provided

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Job Description:

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.

Job Responsibility:

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

Requirements:

Degree in Pharmacy, Biotechnology, Chemistry, or another scientific discipline
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
Solid knowledge of GMP and regulatory guidelines (FDA, EMA, ICH)
Familiarity with IQ/OQ/PQ protocols and risk assessment methodologies
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

Nice to have:

Experience with filling lines and freeze-dryers
Fluency in English and French

What we offer:

Contribute to high-impact validation projects in a reputable pharmaceutical company
Gain valuable experience in GMP and regulatory-driven environments

Additional Information:

Job Posted:
May 09, 2025

Expiration:
July 31, 2025

Employment Type:

Fulltime

Work Type:

On-site work

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