C&Q Consultant: GMP Validation for Life Sciences

Syntegon Technology GmbH

Lisboa

On-site

EUR 42,000 - 64,000

Full time

5 days ago

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Job summary

Syntegon Telstar is seeking a Commissioning & Qualification Consultant to support Life Sciences clients in Portugal. You will lead and participate in CQ projects, ensuring GMP compliance and effective equipment qualification across multiple sites.

The role combines hands-on testing with client interaction and ongoing professional growth. Ideal candidates have a university engineering/IT/chemical/biotech/pharma background, English fluency, and a proactive, analytical mindset.

Qualifications

University degree in engineering/IT/chemical/biotech/pharma or similar.
No experience or 2+ years in equipment/utilities qualification in Life Science.
Solid GMP/regulatory understanding and validation principles.
Fluent English (written and spoken).
Strong analytical skills and proactive attitude.
Excellent communication and interpersonal skills, travel availability.

Responsibilities

Participate and lead commissioning and qualification projects in the pharmaceutical industry.
Plan and manage project activities according to client needs and GMP practices.
Prepare and review key documents: CQ Plan, Protocols, URS, DQ/IQ/OQ/PQ, Traceability Matrix.
Execute qualification tests and support investigations.
Collaborate with client teams to define strategies and ensure timely delivery.
Contribute to continuous improvement of internal processes.