Hovione, an independent, family-owned international group, is a leading Contract Development and Manufacturing Company serving the pharmaceutical industry. We're a global team of over 1950 members from 36 countries, committed to innovation and excellence. This is a fantastic opportunity to join our team in Loures, Portugal.
🚀 What You'll Do:
- Ensure project and product activities comply with cGMP requirements and maintain our Quality Management System.
- Manage and participate in key quality activities for assigned products/projects, including documentation preparation, review, and approval.
- Support internal and external audits and inspections, reviewing action plans.
- Maintain inspection readiness and advise on internal/external audits.
- Follow up on deviations and Change Controls (PdAs) for timely closure and approval.
- Prepare SOPs, IOPs, quality reports, and change control documents (PdAs).
- Review process documentation, batch documentation, and product specifications.
- Review regulatory documentation and coordinate site documentation.
- Authorize production equipment/utility usage when qualification is needed.
🔎 What We're Looking For:
- University degree: Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a similar scientific field.
- Experience: Prior experience in a chemical environment is a plus.
- Language: Fluency in English is required.
- Computer Skills: Proficiency in MS Office Suite.
- Attention to Detail: Excellent documentation skills and meticulous attention to detail are essential.
📍 Location: Loures, Portugal (Onsite)
About Hovione:
Hovione is an international leader in pharmaceutical contract development and manufacturing, dedicated to helping customers bring new and off-patent drugs to market. We value innovation, excellence, and our diverse global team. We are committed to inclusion and diversity, fostering a respectful and supportive work environment.