Life Sciences C&Q Consultant - GMP & Validation Expert

Syntegon Technology GmbH

Lisboa

On-site

EUR 30,000 - 52,000

Full time

25 hours ago
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Job summary

Syntegon Telstar in Portugal seeks a Commissioning & Qualification Consultant to support GMP-compliant equipment qualification and validation projects in the Life Sciences sector.

You will lead and assist with commissioning activities, review CQ documentation, and collaborate with client teams across Portugal. Travel availability is required; English fluency is essential as projects involve international clients.

Qualifications

  • University Degree in Engineering, IT, Chemical, Biotechnology, Pharmaceutical Sciences or similar.
  • No experience or 2+ years of experience in equipment and/or utilities qualification within Life Science industry.
  • Solid understanding of GMP regulations and validation principles.
  • Fluent in English (written and spoken).
  • Availability to travel.

Responsibilities

  • Participate and lead commissioning and qualification projects in the pharmaceutical industry.
  • Plan and manage project activities according to client needs, regulatory requirements, and GMP best practices.
  • Prepare and review key project documentation (e.g., Commissioning and Qualification Plan, Commissioning Protocols, VMP, URS, RA, DQ, IQ, OQ, PQ, Traceability Matrix, etc.).
  • Execute qualification tests and support technical investigations.
  • Collaborate with client teams to define strategies, propose solutions, and ensure timely project delivery.
  • Contribute to the continuous improvement of internal processes and methodologies.

Skills

Fluent English
Strong analytical skills
Proactive approach
Dynamic attitude
Excellent communication
Interpersonal skills
Availability to travel

Education

University degree in Engineering/IT/Chemical/Biotechnology/Pharmaceutical Sciences or similar

Job description

Syntegon Telstar in Portugal seeks a Commissioning & Qualification Consultant to support GMP-compliant equipment qualification and validation projects in the Life Sciences sector.

You will lead and assist with commissioning activities, review CQ documentation, and collaborate with client teams across Portugal. Travel availability is required; English fluency is essential as projects involve international clients.

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