C&Q Consultant for Pharma Industry

SYNTEGON; Lisboa; Presencial; EUR 40 000 - 60 000; Tempo integral

Resumo da oferta

SYNTEGON is seeking a motivated and detail-oriented Commissioning & Qualification Consultant to join our consultancy team in Barcarena, Portugal. This role involves leading commissioning and qualification projects in the pharmaceutical industry, ensuring compliance with GMP standards while preparing key project documents.

The ideal candidate will have a university degree in Engineering, Chemical, Biotechnology, or Pharmaceutical Sciences, alongside strong analytical skills and excellent communication abilities. This is a great opportunity to enhance your expertise in the Life Sciences sector.

Qualificações

• Experience in equipment and utilities qualification.
• Understanding of GMP regulations and validation principles.
• Fluent in English.

Responsabilidades

• Lead commissioning and qualification projects.
• Manage project activities as per client needs.
• Prepare and review project documentation.
• Execute qualification tests and support investigations.
• Collaborate with client teams for project strategies.
• Contribute to process improvements.

Conhecimentos

Pharmaceutical compliance

Utilities qualification

Strong analytical skills

Excellent communication

Formação académica

University Degree in Engineering, Chemical, Biotechnology or Pharmaceutical Sciences

Descrição da oferta de emprego

Scope: Commissioning & Qualification Consultant – Life Sciences Industry

We’re looking for a motivated and detail-oriented C&Q Consultant to join our consultancy team in Barcarena. If you already have experience in equipment and utilities qualification and are eager to deepen your expertise in pharmaceutical compliance and validation, this is your opportunity to work on impactful projects across the Life Sciences sector.

Functions

• 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.

Requirements

• University Degree such as Engineering, Chemical, Biotechnology, Pharmaceutical Sciences or similar.
• 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.