Job Details
- Contract Type:
- Unlimited / Full-Time
- Country / City:
- Spain / Argentona
- Company:
- Beiersdorf Manuf. Argentona
- Job Function:
- Quality Management
Your Tasks
Being the site head for QM, QC and Regulatory Affairs
Act as the main contact and person responsible with the Spanish health authorities.
Ensure compliance for manufacturing, release of finished goods and material/pharmacovigilance.
Lead the production center Quality team
Maintain and improve the site QMS (GMP/ ISO)
Lead and conduct internal and external audit
Host, support and lead audits from the notified body and authorities
Manage complaint handling, NC/CAPA, changes, corrective field actions and continuous improvement with the team
Supervise Quality Control, validations (process, test method, software) 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 Quality / Regulatory roles (Medical Device and/or Pharmaceutical manufacturing...).
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.
