Quality Assurance Consultant for Pharma Industry at Azbil Telstar UK Ltd

Lisbon, , Portugal -

Full Time

Start Date

Immediate

Expiry Date

26 May, 26

Salary

0.0

Posted On

25 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, GMP Compliance, Quality Systems Implementation, Validation Activities, Audit Support, Inspection Support, Deviation Management, Batch Dossier Review, SOP Preparation, Regulatory Requirements, Analytical Skills, Communication Skills, Technical Support, Continuous Improvement, Risk Analysis, Data Analysis

Industry

Machinery Manufacturing

Description

Company 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. Job Description 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. Qualifications 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! Functional Area (career page): Quality Management & Validation Working hours: Full-time Legal Entity: Soc. De Servicios de Engenharia à Ind. Farmacèutica Ltd.

Responsibilities

The consultant will execute Quality Assurance activities for pharmaceutical projects, including Deviation Management and Batch Dossier Review, while preparing and reviewing essential project documentation like SOPs, Validation Protocols, and Audit Reports. They must ensure strict compliance with industry standards, including GMP and applicable pharmaceutical regulations, and contribute to continuous improvement initiatives.