Job Description

Join Syntegon Telstar and Be Part of Something Extraordinary!

At Syntegon Telstar, our success starts with the people. Every day, our team is guided by values that define who we are: Customer First, Enjoy Working Together, Learn Constantly, Honesty and Openness, and Strive for Excellence. These principles are not just words – they are the foundation of a culture that drives excellence in every project we undertake. As part of Syntegon, a global leader in processing and packaging technology, Telstar benefits from a strong international presence and cutting-edge expertise.

With 20 years of experience in Portugal, Syntegon Telstar has built a solid reputation as a trusted partner for the pharmaceutical industry, providing expert consultancy and innovative solutions tailored to local and global market needs.

We know that our work makes a difference. By delivering high-quality solutions, we empower our clients in the Life Sciences industry, helping them achieve success in a highly regulated and rapidly evolving sector. Collaboration and mutual respect are at the heart of everything we do, creating an environment where every idea matters, and every voice is heard.

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.

Scope: Junior CSV Consultant – Life Sciences Industry

We're looking for curious and driven minds to join our consultancy team in Barcarena No experience? No problem. We value talent, a passion for learning, and a desire to make an impact in healthcare and life sciences.

As a Junior CSV Consultant, you’ll work alongside a dynamic team supporting pharmaceutical companies in Portugal, contributing to exciting projects that truly matter. You’ll be involved in projects focused on GMP compliance, CSV (Computer System Validation), and specialized consultancy. You will provide technical support to ensure our clients meet the highest standards in regulated environments. It’s a hands-on role where you’ll learn fast, grow your expertise, and make a meaningful impact from day one.

Functions:

• Participate in and develop Computer System Validation (CSV) projects for pharmaceutical industry clients.
• Manage projects in compliance with client requirements, regulatory frameworks (GxP, FDA 21 CFR Part 11, EU Annex 11), and industry best practices.
• Write and review validation documentation, including Validation Plans, Protocols (IQ, OQ, PQ), and Validation Reports.
• Perform validation activities such as risk assessments, qualification testing, and regulatory impact analysis.
• Present and discuss project solutions to clients and within internal team.

Qualifications

Requirements:

• University Degree such as Engineering, IT, Chemical, Biotechnology, Pharmaceutical Sciences or similar.
• Fluent in English (written and spoken).
• Strong analytical skills, proactive approach, and dynamic attitude.
• Excellent communication and interpersonal skills.
• Availability to travel.

Additional Information

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!