Commissioning & Qualification Consultant - Pharma

About the role

Syntegon Telstar, a GMP consultancy for the pharmaceutical industry with 20 years of experience in Portugal, is looking for a Commissioning & Qualification (C&Q) Consultant to join its team in Barcarena. The consultant works with multidisciplinary teams supporting Life Science companies in Portugal, contributing to projects that ensure GMP compliance and equipment qualification and validation.

Key responsibilities

• Take part in 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 documentation such as commissioning plans, protocols, VMP, URS, RA, DQ, IQ, OQ, PQ and traceability matrices.
• Carry out qualification tests and support technical investigations.
• Work with client teams to define strategies, propose solutions and deliver projects on time.
• Contribute to the continuous improvement of internal processes and methodologies.

Required profile

• University degree in Engineering, IT, Chemical, Biotechnology, Pharmaceutical Sciences or similar.
• No experience or 2+ years of experience in equipment and/or utilities qualification in the Life Science industry.
• Fluent English, written and spoken.
• Availability to travel.

Required skills

• Solid understanding of GMP regulations and validation principles.
• Strong analytical skills, proactive approach and excellent communication skills.

What we offer

• A leading GMP consultancy team working with top-tier pharmaceutical clients.
• Hands-on experience interacting directly with clients across Portugal.
• A collaborative environment that supports professional development.
• The chance to work for a company with a worldwide presence in the Life Sciences industry.