QA Specialist - Clinical Research

☞ SGS

Visualizza: 175

Giorno di aggiornamento: 26-11-2025

Località: Mechelen Antwerp

Categoria: R & D

Industria: Oil Gas Retail Office Equipment Consumer Services

Tipo di lavoro: Full-time

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Contenuto del lavoro

Company Description

At SGS, you can choose!

First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call ‘connectors’, people who can connect our diversity to our services. To each other. And this way, enrich our business.

SGS is the world’s leading inspection, verification, testing and certification company. We’re also the worldwide benchmark for quality and integrity. And that makes us very proud. This can only happen thanks to more than 90 000 colleagues worldwide, with 1650 employees in Belgium only. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.

The Quality Assurance Department is an independent department within SGS Clinical Research. It is responsible for the Quality Management System, which covers all quality documents, training and qualification, resolution and documentation of deviations, auditing activities and dedicated quality support to all operational teams (i.e. Clinical Pharmacology Unit, Clinical Operations, Biometrics and Medical Safety & Regulatory, and Business Development and Support).

We are currently looking for a QA Specialist - Clinical Research!

Job Description

As QA Specialist - Clinical Research you are welcomed in a smaller, amiable, and enthusiastic QA team where you will have day-to-day interaction with other QA experts in the field, such as other OQMs, Quality Compliance Managers, Auditors, …

You are an indispensable partner of the operational teams in the management of their part of the quality system. By supporting the operational teams, you will gain further insight into the different phases and activities involved in the conduct of clinical trials for pharma and biotech companies from start to finish.

Your Main Responsibilities Are The Following
  • Develop and maintain operational quality and personnel documents (SOPs and WIs, manuals and various guidance documents) in collaboration with the assigned operational teams
  • Propose changes to operational quality documents in order to improve the quality system
  • Initiate process improvements / efficiencies were needed
  • Monitor quality by following up on timely training of new or revised quality documents
  • Guide the teams through the deviation management process by assisting in risk assessment of deviations, Root Cause Analyses and formulation of CAPA Plans
  • Assist the teams in performing their daily work in a consistent and efficient way
  • Participate in / facilitate cross-functional discussions and working groups related to any aspect of quality, to create or optimize cross-functional procedures, or to look for efficiencies in processes and collaboration
  • Overall – collaborate with the assigned operational teams to improve quality and maintain high quality standards throughout the organization
Qualifications

What do you need to be successful?!
  • Minimum of 3 years of experience in a CRO or university research (department, laboratory) setting, or in a pharmaceutical, biotech, medical devices (or similar) company, or equivalent by combination of education, training and experience
  • Fluently writing and speaking English
  • Excellent communication and problem-solving skills
  • Strong organizational skills
  • Proficient in writing
  • Good knowledge of MS office
  • Assertive and motivated
  • Open for discussion and constructive attitude
  • Strive for quality and eye for detail
  • Stress resistant and flexible
  • Good knowledge of ICH-GCP, good documentation practices, experience with eTMF / filing, or project management are an asset
We are looking for someone who is passionate about quality and ready to work on exciting projects within Clinical Research. If you are looking to advance your career, enhance your skills and build connections, this position is definitely for you!

Additional Information

What we have to offer:

Were you already considering a big switch or anext step in your career?

Maybe this could be your next step! At SGS we can offer you the following:
  • An interesting position where you can take responsibility
  • An open work atmosphere in an international setting with equal opportunities for all employees
  • A dynamic environment that fosters innovation and inspires employees to drive the business forward proactively and generate success
  • Opportunities for personal development by continued education
  • Good work-life balance with possibility of working from home
  • Coffee corners and sandwiches in the cafeteria during lunch
  • Regular social events (i.e. happy hours)
  • A permanent contract with competitive salary package (incl. company car, work laptop/cellphone, retirement plan, meal vouchers, …)
Do you want to be part of this?

We are looking forward to hearing from you!

Send us your story and your resume via the apply button and maybe you will soon join us for work and coffee breaks.

Still have questions?

Heidi Aerts can give you more details about the job. Send her an e-mail at heidi.aerts@sgs.com
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Scadenza: 10-01-2026

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