Stability Reviewer

Description
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
Stability Reviewer
to join our
Quality Control
team in our
Pallini premises
.

As a
Stability Reviewer
, the ideal candidate will be responsible for reviewing all data generated during release and stability testing and for completing the relevant stability documentation.

Requirements
More particularly:

What You Will Do

• Review analytical release and stability raw data for both commercial and non-commercial products, ensuring timely completion and compliance with cGMP requirements
• Conduct laboratory investigations to resolve non-conforming or out-of-trend data and liaise with clients regarding any non-conformances
• Collect and verify all necessary data (e.g., specifications, certificates of analysis) for the preparation of stability study protocols and cards
• Monitor each product's stability program, as defined by its respective protocol
• Collaborate closely with cross-functional teams to ensure alignment on stability team requirements
• Collaborate with stability analysts to ensure accurate and complete stability data
• Communicate the results of the review to relevant parties

The Ideal Candidate Should Have

• Minimum a BSc Degree in Chemistry or relevant field
• At least 2 years of experience within a pharmaceutical environment/Quality control
• Experience in a GMP or GLP environment

Job-Specific Skills

• Excellent communication in English language (writing & speaking)
• Strong problem solving 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.