About the role

Aplyr's Quick Take

This role is focused on ensuring the quality and compliance of pharmaceutical products before they reach patients. You'll be working closely with production and quality control teams to manage the release of materials and products, investigate issues, and contribute to process improvements. It's an individual contributor role requiring expertise in QA within the pharmaceutical sector.

Good fit

Ideal candidates have a master's degree in a scientific field and experience in the pharmaceutical industry, particularly with Good Manufacturing Practices. Strong communication skills and the ability to collaborate across teams are essential.

Worth noting

The position is based in Belgium and does not offer relocation support, so applicants must already be local. There's a possibility to act as a Qualified Person, which could be a unique opportunity for those with the right background.

Salary Range:

€47,100.00 - €87,500.00

Job Description Summary

Location: Puurs, Belgium
Relocation Support: This role is based in Puurs, Belgium. Novartis is unable to offer relocation support: please only apply if accessible.

Join a team where your work directly ensures the timely and compliant release of high‑quality products to patients. In this position, you’ll apply your QA expertise to assess quality and compliance, support investigations and keep essential processes running smoothly. You’ll collaborate closely with production teams, QC laboratories, other QA departments, MS&T, Supply Chain and external partners to resolve issues, reduce deviations and strengthen supply reliability. Your contributions to audits, CAPAs, and continuous improvement will uphold quality standards and make a meaningful impact across our operations and for the people relying on our medicines.

Job Description

Major accountabilities:

Ensure compliant and timely release of raw materials, bulk products, packaged goods, sterilizations, and imported batches.
Maintain up‑to‑date expertise in production, sterilization, and release processes relevant to assigned responsibilities.
Review and assess non‑conformities, support investigations, and define effective CAPAs.
Contribute to initiatives that reduce deviations and strengthen overall process robustness.
Monitor file and batch status versus targets and follow up on problem or priority lots.
Communicate effectively with logistics teams, QC laboratories, and external partners on release‑related matters.
Provide clear explanations of QA release documentation during internal and external audits.
Keep assigned procedures accurate, updated, and aligned with evolving operational requirements.

Essential Requirements:

Master’s degree in a scientific field such as Pharmacy, Industrial Pharmacy, Bio‑engineering, or related discipline.
Experience within the pharmaceutical industry.
Strong understanding of Good Manufacturing Practices and relevant pharmaceutical legislation.
Proficiency in computer systems with the ability to work accurately with digital documentation.
Excellent communication skills both in English and Dutch. Ability to collaborate effectively across teams and with external partners.

Desirable Requirements:

Ability or prior experience to act as a Qualified Person (QP) in accordance with applicable regulatory requirements.

At Novartis, we’re committed to reimagining medicine together- and rewarding the people who make it happen.

Expected Annual Base Salary Range: 47.100 - 87.500 EUR.

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with theNovartis pay setting policy and upon joining Novartis will be reviewed
periodically.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans,retirement
plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

Commitment to Diversity and Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Skills Desired

Collaboration, Communication, Data Integrity, Good Manufacturing Practices (GMP), Internal Quality Auditing, Managing Ambiguity, Operational Excellence, Quality Assurance (QA), Quality Compliance, Quality Control (QC), Quality Management Systems (QMS), Regulatory Compliance, Standard Operating Procedure (SOP), Statistical Process Control (SPC)

Aplyr's read

Novartis is a Swiss-based global healthcare leader, known for its focus on innovative medicines and commitment to addressing patient needs through diverse roles.
Synthesized from recent postings & public sources

What's promising

•Novartis invests heavily in research and development, driving innovation in pharmaceuticals.
•The company offers a wide range of global career opportunities across various fields.
•Strong focus on cutting-edge therapies, including gene therapy and AI-driven solutions.

What to watch

•Regulatory challenges can impact the speed of drug approval and market entry.
•High competition in the pharmaceutical industry requires constant innovation to maintain market position.
•Complex organizational structure may slow decision-making processes.

Why Novartis

•Novartis has a robust pipeline of innovative medicines, setting it apart in the healthcare sector.
•The company emphasizes a diverse and inclusive workplace culture across its global operations.
•Novartis is a leader in digital transformation within pharmaceuticals, integrating AI and data science.

Aplyr’s read is generated by AI from public sources. Was it useful?

About Novartis

Novartis

novartis.com

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Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. It focuses on innovative medicines, generics, and eye care.