Control Products for Exports Reviewer

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 Control Products for Exports Reviewer to join our Quality Control team in our Pallini premises. 

As a Control Products for Exports Reviewer, the ideal candidate will ensure compliance to GMP standards through appropriate reviewing.

Requirements

More particularly:

What you will do:

• Conduct detailed reviews of batch records for completeness, accuracy, and compliance with GMP, SOPs, and regulatory requirements
• Ensure all discrepancies, deviations, and non-conformances are properly documented, investigated, and resolved before batch release
• Collaborate with manufacturing, quality control, and other departments to ensure batch records meet all quality and compliance standards
• Provide recommendations for improvements in batch record documentation processes

The ideal candidate should have:

• Minimum a BSc Degree in Chemistry or relevant field
• At least 2 years of experience in pharmaceutical product analysis
• Experience in a GMP or GLP environment

Job-Specific Skills:

• Excellent communication in English language (writing & speaking)
• Competent in laboratory instrumentation (e.g., HPLC, GC, dissolution)
• Experience in oral, solid and finished drug production
• Exceptional problem-solving and critical-thinking skills
• Excellent verbal and written communication skills
• Computer literacy

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.