Job Details
- Contract Type:
- Unlimited / Full-Time
- Country / City:
- Spain / Argentona
- Company:
- Beiersdorf Manuf. Argentona
- Job Function:
- Quality Management
Your Tasks
Act as Qualified Person and main contact with health authorities.
Ensure regulatory compliance for manufacturing, import, release and pharmacovigilance.
Lead the Quality team and oversee QMS (GMP/ISO): batch release, audits, deviations, complaints and recalls.
Supervise Quality Control, validations and staff training.
Drive continuous improvement in products, processes and supplier quality.
Promote safety, compliance and best practices within the organization.
Your Profile
Degree in Chemistry or related field.
At least 5–7 years of experience in pharmaceutical Quality/Regulatory roles.
Proven experience leading Quality teams.
Solid knowledge of GMP, ISO standards and EU regulatory framework.
Strong communication and leadership skills, with ability to interact with authorities.
Languages: fluent in English (written and spoken); Spanish required; Catalan is a plus.
Additional information
All qualified applicants will receive consideration for employment without discrimination on the basis of race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, age and genetic information.
