QA Reviewer

Abacus Medicine Group; Alkmaar; On-site; EUR 32,000 - 42,000; Full time

Job summary

Abacus Medicine Group in Alkmaar, Netherlands is hiring an entry‑level Quality Assurance Reviewer to ensure medicinal products are reviewed in full GMP compliance before release. You will collaborate with QA teams and cross‑functional colleagues to safeguard product quality and patient safety.

The role requires an MBO level qualification, strong English, independent working skills and a meticulous approach to documentation. Dutch language is a plus, and a 40‑hour work week is preferred.

Qualifications

• MBO level or higher (working and thinking level)
• Entry‑level position; prior regulated/pharmaceutical experience is an advantage but not required
• Basic knowledge of GMP principles and interest in pharmaceutical quality assurance
• Strong written and spoken English; Dutch is a plus
• Ability to work independently, manage responsibilities and priorities to meet deadlines
• Highly accurate, detail‑oriented, with thorough documentation practices

Responsibilities

• Review production documentation to ensure medicinal products are manufactured/repackaged in compliance with GMP and MA requirements
• Review Batch Journals and photo samples; prepare batches for Qualified Person release
• Ensure review activities are completed accurately and within required timelines
• Contribute to maintaining and improving the review process; update Quality Management System documentation
• Communicate with internal stakeholders to resolve deviations and support batch documentation questions
• Assist in archiving and administering Batch Journals and related records across sites

Job description

Drive meaningful change

Are you quality-driven, detail-oriented and eager to contribute to patient safety? We are looking for a proactive Quality Assurance (QA) Reviewer who ensures that medicinal products are reviewed accurately and in full compliance with GMP requirements before they are released to the market. In this role, you will play an important part in safeguarding product quality and ensuring patients receive safe and compliant medicines.

Drive meaningful change

Are you quality-driven, detail-oriented and eager to contribute to patient safety? We are looking for a proactive Quality Assurance (QA) Reviewer who ensures that medicinal products are reviewed accurately and in full compliance with GMP requirements before they are released to the market. In this role, you will play an important part in safeguarding product quality and ensuring patients receive safe and compliant medicines.

Get a glimpse of the team

You will be based in Alkmaar and become part of the Quality Assurance department, working alongside QA Reviewers, QA Officers, Qualified Persons and the Team Lead QA Review. Currently the QA reviewing team consists of 5 colleagues. You will also collaborate closely with colleagues from Operations, Repackaging, Supply Chain and our Quality teams in Denmark and Hungary to ensure an efficient and compliant review and release process.

Your Main Responsibilities

As QA Reviewer, you are responsible for reviewing production documentation to ensure medicinal products have been manufactured and repackaged in accordance with the Master Batch Journal, the Marketing Authorisation and applicable GMP regulations. You review completed Batch Journals, verify documentation and photo samples, prepare batches for Qualified Person release and ensure all review activities are completed accurately and within the required timelines.

Alongside your operational responsibilities, you contribute to maintaining and continuously improving the review process. You communicate closely with internal stakeholders to resolve deviations, support colleagues with batch documentation questions, assist in updating Quality Management System documentation, approve reprocess forms and ensure Batch Journals are administered and archived correctly. By collaborating across departments and sites, you help ensure an efficient and compliant release process.

Fuel for your success in the role, we imagine you have:

• At least a MBO working and thinking level or equivalent;
• This is an entry-level position, experience within a regulated or pharmaceutical environment is an advantage, but not required;
• Basic knowledge of GMP principles and an interest in pharmaceutical quality assurance and batch review processes;
• Strong communication skills in English, both written and verbal; Dutch is considered an advantage;
• The ability to work independently, manage your own responsibilities and prioritize tasks effectively to meet deadlines;
• A highly accurate and detail-oriented approach, ensuring documentation is reviewed thoroughly and consistently;

We strongly prefer candidates who are available to work 40 hours per week.

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Moving Healthcare. Moving You.

In Abacus Medicine Group, you’ll experience the power of Moving Healthcare. With our change mindset, we're moving the industry and improving healthcare as we broaden access to medicine.

But it's not just about moving healthcare, it's about Moving You. You’ll be part of a caring community of more than 1,800 people across the World. With us, you will be valued, empowered, and have a direct impact on driving change. Let's access the future of medicine and make a difference together. Your move.