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 QMS Officer (fixed term) for the Corporate Quality Management team in our Marousi premises.

As a QMS Officer, you will assure compliance to the GMP standards and ISO requirements by maintaining an accurate and up to date QA database.

More particularly:

What you will do:

• Ensure compliance of the Quality Management System’s Requirements according to International Standard ISO 9001
• Access and use of the software provided by ΙΤ of company and is related to their work as, eQMS, Training Tools and Systems, e-signature tools
• Take part in the authorship of the department’s SOPs, TDRs, protocols and any other kind of controlled quality document
• Handling, monitoring of overall Quality Management database system
• Coordinating main department’s processes such as “Corrective Preventive Actions”, “Deviation Investigation Reports” and “Change Control Mangement” in eQMS
• Coordinating “Risk Management” procedure
• Preparing and monitoring quality metrics for the main department’s processes
• Support audits/inspections, regarding Deviation, Risk, CAPA, Change requests
• Develop quality documents in compliance with the registered and approved product review
• Handling and submission of registration/compliance related requests to foreign countries
• Ηandling requests related to quality aspects, for submission either to the Greek Health Authorities (NOM) or to foreign Health Authorities

Requirements

The ideal candidate should have:

• BSc / MSc in Chemistry, Pharmacy or equivalent field
• Desirable 1-2 years’ experience in Quality Management or relevant department

Job-Specific Skills:

• Excellent communication in English language (writing & speaking)
• Computer literacy
• Ability to prioritize tasks and meet deadlines
• Exceptional communication skills, strong project management skills

Benefits

What you'll gain:

• Involvement in a high-caliber, team-oriented and dynamic atmosphere
• Exposure to challenging business issues and practices
• Great opportunity to leverage and develop your business knowledge and skills

Join our team and experience the unique Pharmathen’s culture that gives you the opportunity to innovate, to make decisions, to achieve your own potential and to chart your own career.

Pharmathen is an equal opportunity employer. We welcome applications regardless of gender, race, age, religion, sexual orientation, and national origin.