Manage the QA team and ensure compliance with EU-GMP and USFDA regulations while overseeing GMP requirements and quality systems.
At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are currently looking for a high-performing Quality Assurance Manager. The position is based in Tripoli.
Main duties and responsibilities:
- Lead and manage the QA team, overseeing daily operations and long-term strategy.
- Ensure compliance with EU-GMP and USFDA regulations.
- Oversee the implementation of GMP requirements and the company’s QMS for establishing new production lines for injectable formulations and active product ingredients (APIs).
- Issue and monitor the Validation Master Plan for new production lines.
- Review Standard Operating Procedures (SOPs).
- Maintain continuous collaboration and communication with other departments, including Production, Technical and Quality Control.
- Oversee Change and Risk Management for the project plan.
- BSc Degree in Chemical Engineering, Chemistry, or Pharmacy. MSc Degree in Quality Management or a related field is considered an asset.
- A minimum of 5 years of experience in Quality Assurance within the pharmaceutical industry and in pharmaceutical quality systems.
- Experience with authorities’ inspections (PIC/s, USFDA) is considered an asset.
- Ability to work creatively, analytically and synthetically with great attention to detail.
- Fluency in Greek and English.
- Proficiency in computer literacy.
- Ability to communicate expectations clearly and ensure that all team members meet quality standards.
- Self-motivated and results-oriented with the ability to cope with strict timelines.
The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.
Top Skills
Gmp
Qms
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