Quality Assurance Associate | Temporary (6 Months)

Breda, reference 2026-01202

Job description

This role is crucial for ensuring the quality and compliance of essential product documentation and master data. As a Quality Assurance Associate, you will play a vital part in safeguarding product integrity by meticulously reviewing and approving critical information. The ideal candidate will thrive in an environment that demands precision and a strong compliance mindset, contributing directly to the company's commitment to excellence.Your key responsibilities will include:

•  Performing detailed quality reviews and approvals of artworks for various products.
•  Conducting thorough quality checks and approvals for Bill of Materials (BOMs).
•  Reviewing and approving critical fields within the master data system to ensure accuracy and compliance.
•  Executing precise checks and verifying information against established procedures and regulatory standards.
•  Collaborating effectively with team members to manage workload distribution and ensure timely completion of tasks.
•  Identifying potential issues or discrepancies and proactively following up to ensure their resolution.
•  Adhering strictly to Good Manufacturing Practice (GMP) guidelines and internal quality procedures.

Please note that we are unable to consider candidates who require visa sponsorship or who live too far from the work location. Candidates who would need to relocate can only be considered if they have already secured accommodation within a reasonable commuting distance.

Requirements

We are looking for a highly detail-oriented and compliance-minded individual who is eager to contribute to a rigorous quality assurance process. You should possess a strong sense of responsibility, excellent communication skills, and a collaborative spirit to work effectively within a diverse team. The ideal candidate is proactive in identifying issues and committed to understanding the importance of accurate checks in a regulated environment. Character and mindset are paramount for success in this role.

•  English – C1 (spoken and written)
•  Relevant educational background (e.g., Bachelor's or Master's degree in a scientific field)
•  Some relevant in a regulated industry (e.g., Pharma, Food) is highly preferred
•  Ability to perform highly detailed and precise review tasks
•  Strong collaborative and communication skills
•  Proficiency in standard office software; familiarity with SAP is a plus but not required

Working conditions

• This is a 6-month contract position through Undutchables, with the possibility of future opportunities within the company, though no guarantees can be made for an extension in this specific role.
•  Working hours: Full-time (40 hours/week) is preferred, but 32 hours/week is also an option.
•  Hybrid work model: During the initial training period (approx. 1.5 months), you will be expected to be on-site 3-4 days per week. After training, a minimum of 2 days per week on-site is required, with Thursdays being a fixed office day.
• Competitive salary package.
• Pension scheme
• Travel expense reimbursement, dependent on distance.
• Dynamic, international, and collaborative work environment with excellent development opportunities.

Work location

Breda Our client is a leading international company in the pharmaceutical industry, focused on ensuring reliable, efficient, and high-quality manufacturing and distribution operations worldwide. The company culture is international, collaborative, and fast-paced, with strong attention to quality, compliance, and continuous improvement. Employees have the opportunity to work on cross-regional projects, standardize global processes, and contribute directly to operational excellence in warehousing and distribution.

Good to know

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Website: 2027-02-24

Recruiter contact

Anique van Gorp, Eindhoven
anique.vangorp@undutchables.nl
+31(0)6-28514242