We are looking for a Deputy Manager responsible for overseeing and providing operational support as well as ensuring compliance within the Medicinal Products Department. Key responsibilities include managing the packaging process daily, coordinating investigations related to non-conformities (NC), implementing corrective and preventive actions (CAPA), and ensuring compliance with GMP requirements.
The person in this role will act as a liaison between the production, quality assurance, engineering, and regulatory departments, supporting audits and continuous improvement initiatives.
Responsibilities:
- Supervise packaging operations and ensure compliance with schedule and GMP standards.
- Lead or support investigations regarding deviations, NCs, and complaints.
- Perform root cause analysis and implement effective CAPA.
- Create, review, and approve operational and quality documentation (SOPs, batch records).
- Participate in internal and external audits as a quality representative.
- Train the team on GMP, data integrity, and good investigation practices.
Qualifications:
- Experience in medicinal product packaging or pharmaceutical manufacturing.
- Experience in team management.
- Knowledge of GMP regulations.
- Ability to conduct quality analyses and prepare documentation.
- Fluent English (mandatory).
- Ability to collaborate in a cross-functional environment.
Join us in our mission to make a positive impact on healthcare through innovation and excellence in manufacturing.
