C&Q Consultant – Life Sciences GMP Validation Expert

Telstar; Barcarena; On-site; EUR 40,000 - 60,000; Full time

Job summary

Syntegon Telstar is seeking a Commissioning & Qualification Consultant for the Life Sciences sector in Barcarena, Portugal. You will support GMP-compliant equipment qualification, lead projects, and collaborate with multidisciplinary teams across Portugal.

The role combines hands-on technical work with client interaction and ongoing professional growth, offering exposure to global pharma clients and complex validation activities.

Qualifications

• University Degree such as Engineering, IT, Chemical, Biotechnology or Pharmaceutical Sciences or similar.
• No experience or 2+ years of experience in equipment and/or utilities qualification within the Life Science industry.
• Solid understanding of GMP regulations and validation principles.
• Fluent in English (written and spoken).
• Strong analytical skills, proactive approach, and dynamic attitude.
• Excellent communication and interpersonal skills.
• 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

English fluency

Analytical skills

Communication skills

Travel availability

Education

University degree in Engineering/IT/Chemical/Biotech/Pharma

Job description

Syntegon Telstar is seeking a Commissioning & Qualification Consultant for the Life Sciences sector in Barcarena, Portugal. You will support GMP-compliant equipment qualification, lead projects, and collaborate with multidisciplinary teams across Portugal.

The role combines hands-on technical work with client interaction and ongoing professional growth, offering exposure to global pharma clients and complex validation activities.