QA CONSULTANT - DRUG PRODUCT MANUFACTURING

QA Consultant – Drug Product Manufacturing Location: Hillerød, Zealand Region Category: Quality and Compliance Salary: Apply for details Country: Denmark Employment: Contract Worksite: On-Site Job Description 3 month contract · full time · on-site A leading international biopharmaceutical manufacturing organisation is seeking an experienced Senior DPM Quality Assurance Associate to support operations within a sterile Drug Product Manufacturing environment. The Opportunity Working closely with the Quality Assurance team, you will be responsible for the review and management of key quality records supporting manufacturing operations. This is a hands‑on QA role requiring strong GMP expertise, excellent stakeholder engagement skills and the ability to drive high quality documentation and compliance standards. Key Responsibilities Manage and review deviations and CAPAs within Drug Product Manufacturing Partner with SMEs and investigators to ensure robust investigations and effective corrective actions Review and support change controls, ensuring compliance with quality and regulatory requirements Participate in project kickoff meetings and cross‑functional discussions relating to quality events Review and approve work orders associated with maintenance and equipment activities Support risk assessments and quality documentation activities across the manufacturing facility Collaborate with operational teams to maintain inspection readiness and GMP compliance standards Requirements Minimum 5 years of Quality Assurance experience within the pharmaceutical industry Strong background supporting Drug Product Manufacturing operations Experience managing quality records including deviations, CAPAs, change controls and risk assessments Knowledge of sterile manufacturing and Annex 1 requirements Proven ability to work cross‑functionally with technical and operational stakeholders Excellent communication skills and attention to detail BSc or MSc in Pharmacy, Life Sciences or a related scientific discipline Personal Profile Detail oriented and quality focused Strong team player Effective communicator Commercially aware and solutions driven Comfortable working in a fast‑paced GMP manufacturing environment Equal Opportunity Employer We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements. #J-18808-Ljbffr