Quality Department

Ensuring Safe and High-Quality Pharmaceutical Manufacturing through Stringent Compliance

Minapharm’s Quality Department is primarily focused on promoting strict compliance with quality, safety, and environmental regulations and guidelines.

In close collaboration with other departments, Minapharm’s quality control team validates various processes and ensures all technical procedures are running smoothly. The Department is also in charge of conducting all the required sampling and testing of materials and products to guarantee compliance with regulatory specifications for its premises and equipment. Furthermore, owing to the Department’s regular and ongoing training initiatives, all Minapharm staff remains abreast of quality requirements.

During Minapharm’s 50 years in the market, the company has been committed to implementing the highest safety and quality measures, adhering to the stringent international standards of the European Union, the World Health Organization, and Current Good Manufacturing Practice regulations (CGMPs). Complying with international regulations is especially critical given Minapharm’s many global collaborations with multinational entities, including Abbott, Janssen, JnJ, LEO Pharma, Merck Serono, Novartis, Teijin-Japan, and many more.

Minapharm also guarantees the same protections when it comes to employee health and the environment. To achieve these goals, Minapharm is BSI-certified with ISO 9001, ISO 14001, and ISO 45001 standards.

Minapharm is looking for dedicated Quality Control hires who strive for excellence and are eager to tackle new and developing projects. Potential candidates should be meticulous and detail-oriented and dedicated to fulfilling the company’s longstanding, yet evolving vision of providing affordable and accessible pharmaceuticals.

Have a look at Minapharm’s current vacancies in the Quality Department