QA Consultant – Drug Product Manufacturing

Role overview

This contract role is for an experienced quality assurance professional to support sterile drug product manufacturing operations within a biopharmaceutical environment. The assignment runs for 3 months, is full time, and requires on-site presence in Hillerød, Zealand Region, Denmark.

What you will do

• Take ownership of deviation and CAPA records connected to drug product manufacturing activities.
• Work alongside subject matter experts and investigators to help shape thorough investigations and appropriate corrective actions.
• Assess and support change control documentation to ensure it meets quality and regulatory expectations.
• Join project launch meetings and cross-functional conversations related to quality events.
• Examine and approve work orders tied to maintenance tasks and equipment-related work.
• Assist with risk assessments and broader quality documentation across the manufacturing site.
• Collaborate with operations teams to uphold inspection readiness and GMP standards.

What is required

• At least 5 years of quality assurance experience in the pharmaceutical sector.
• Solid exposure to drug product manufacturing environments.
• Hands-on experience handling deviations, CAPAs, change controls, and risk assessments.
• Working knowledge of sterile manufacturing and Annex 1 expectations.
• Strong ability to partner with technical and operational teams across functions.
• Clear communication skills and strong attention to detail.
• BSc or MSc in Pharmacy, Life Sciences, or another relevant scientific discipline.

Personal attributes

• Highly detail-oriented and committed to quality.
• Collaborative and effective as part of a team.
• Confident communicator.
• Commercially minded and focused on practical solutions.
• Comfortable in a fast-moving GMP manufacturing setting.

Equal opportunity

The employer states that all qualified candidates are considered fairly, without discrimination on the basis of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or other protected characteristics. Inclusive hiring and a respectful workplace are emphasized across all locations. Reasonable accommodations can be requested during the application or interview process for candidates with disabilities or other needs.

Fraud and safety notice

Candidate safety is highlighted as a priority. Applicants are warned about people posing as recruiters to collect personal information. Sensitive data should not be shared with unverified contacts, banking details should never be provided during the application process, and recruiter email addresses should be checked carefully to confirm they use official Planet Pharma domains only.

Additional information

Location: Hillerød, Zealand Region

Country: Denmark

Category: Quality and Compliance

Employment: Contract

Worksite: On-Site

Compensation: Apply for details

3 month contract, full time, on-site.