C&Q Consultant for Pharma Industry

Job Description

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.

As a C&Q Consultant, you’ll collaborate with multidisciplinary teams supporting Life Science companies in Portugal. You will contribute to projects ensuring GMP compliance and equipment qualification and validation, helping clients maintain the highest regulatory standards. This role combines hands-on technical work with client interaction and continuous professional growth.

What we offer:

• A Market Leader in Pharma Consultancy: Join a highly skilled and experienced GMP consultancy team, recognized as a leader in its field.
• Exciting and Meaningful Projects: Work with top-tier pharmaceutical clients and contribute to projects that have a real impact on healthcare and patient safety.
• A Culture of Learning and Support: Gain hands-on experience through direct interaction with clients across Portugal. We provide a collaborative environment where you will be challenged and supported to develop your expertise in the field.
• A Purpose-Driven Career: Be part of a company that provides global solutions for the Life Sciences industry, with a worldwide presence.

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.

Qualifications

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.

Applications:

At Syntegon Telstar, we don’t just hire talent – we build success stories. If you are passionate about making a difference in the Life Sciences industry and want to grow in an environment that values excellence, collaboration, and innovation, we would love to hear from you!

Apply now and take your career to the next level with Syntegon Telstar!