Quality Assurance Consultant for Pharma Industry

Soc. De Servicios de Engenharia à Ind. Farmac • Barcarena

Full-time

Estrada Consiglieri Pedroso 1, 2730-052 Barcarena

from today

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.

Your duties

Scope: Quality Assurance Consultant – Life Sciences Industry

We are looking for a Quality Assurance (QA) Consultant to join our Consultancy Team in Lisbon. We seek professionals with talent, knowledge of quality systems and regulatory requirements, and the motivation to make a difference in the healthcare and life sciences sector.

As a QA Consultant, you will be part of a dynamic team supporting pharmaceutical companies in Portugal, contributing to challenging and high-impact projects. You will be involved in activities related to GMP compliance, quality systems implementation, validation activities, audits and inspections support.

Your role will focus on providing specialized technical support, ensuring that our clients meet the highest standards in regulated environments. This is an opportunity where you will deepen your expertise and actively contribute to meaningful projects from day one.

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:

Execute QA activities for pharmaceutical projects, following established strategies, methodologies, and best practices (e.g., Deviation Management, Batch Dossier Review, etc.).
Prepare and review project-related documentation, including SOPs, RA documents, PQRs, Audit Reports, Manufacturing Instructions, Validation Protocols and Reports, Criticality Analyses, CPVs, Material Risk Analyses, and other QA deliverables.
Ensure compliance with industry standards and regulatory requirements, including GMP and applicable pharmaceutical regulations.
Contribute to continuous improvement initiatives within projects and QA processes.
Stay updated with industry trends, technological advancements, and new methodologies in pharmaceutical QA.

Your profile

Requirements:

Experience in Quality Assurance within the pharmaceutical industry or similar experience.
Master’s degree in Engineering, 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.

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!

Compelling Reasons to join us:

Your Attractive Compensation Package

Benefit from competitive salaries and attractive additional benefits.

Your Work-Life Balance

For a better balance between work and personal life, we support you with flexible working time models.

Your Development

We support your career with personalized training opportunities and promote your career development, for example, through our talent programs.

Your Contribution

Sustainability is part of our identity. We promote a dynamic culture of innovation where you can contribute your ideas and creativity.

Your International Environment

Immerse yourself in an intercultural work environment and work on exciting projects worldwide.

Your Health

We promote health and well-being with a variety of health offerings.

My Job. My Passion.

My passion is to make highly complex packaging systems work to the point.

My passion is to achieve the best result for the department both qualitatively and commercially.

My passion is to make highly complex machines work with just a few lines of code.

My passion is to develop a new machine concept from sketch to fully functional machine.

Get to know us better

Syntegon - Processing and Packaging Technology

Diversity, Equity & Inclusion

Syntegon is a globally operating company that values diversity. We explicitly welcome an environment where all employees, regardless of gender, age, background, religion, sexual orientation, gender identity, or special needs, are equally valued.