Sapes, East Macedonia and Thrace, Greece
75 days ago
Packaging Materials Supervisor (Rodopi)

Founded in 1969, Pharmathen has grown to become one of the largest, vertically integrated developers of complex drug delivery technologies and is among the top 50 pharmaceutical research companies in Europe.

The company has one of the most extensive and advanced pipelines of long acting injectables (LAI), sustained release and ophthalmic formulations.

Pharmathen’s highly diversified portfolio consists of over 90 commercialized products, which are produced in its US FDA and EU-approved manufacturing facilities in Greece, serving 250 customers and accessed by patients in more than 90 countries worldwide.

Pharmathen proudly employs more than 1,600 people from over 28 different nationalities, with 54% of its total workforce and 66% of its Research Operations Team being female. The company’s enduring success is attributed to a passion for creativity, strong ethics, and the dedication of its people, who share a commitment to the company's vision of making a difference in people’s lives.

Due to continuous growth and expansion, Pharmathen Pharmaceuticals offers a great opportunity for career development and is seeking to recruit a Packaging Materials Supervisor for the Quality Control team in our Sapes premises.

As a Packaging Materials Supervisor you will be responsible for ensuring compliance with GMP regarding packaging materials including packaging materials analysis, products release and is also responsible for packaging control.

More particularly:

What you will do:

Handle all matters regarding imported, exported, analyzed, released, or rejected packaging materials Control the accuracy of the supporting documents of all packaging materials used Monitor the progress of all necessary controls, records and approvals of the control files and informs accordingly all involved parts Be responsible for packaging materials’ record keeping Perform the packaging control checks in compliance to the General Procedures and Technical Directives, records and approves the respective quality files and informs the involved parties accordingly Be responsible for packaging materials’ changes and their proper use during packaging procedure. Support the handling, storage, and disposition of retained samples of finished products Have efficient communication with other departments

 

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