Final Products Reviewer (Sapes)
Pharmathen, Greece
Job Description
Pharmathen is one of the leading complex drug delivery and formulation developers and is amongthe top 50 pharmaceutical research companiesin Europe. Driven by innovation, the company specializes in one of the most modern and technologically innovative sectors, developing Long Acting Injectables (LAI), Sustained Release formulations and Preservative Free Ophthalmics.
Pharmathen’s portfolio consists ofover 100 products, produced at its facility in Sapes, Rodopi, approved by the US Food and Drug Administration (FDA), and at its modernized production unit in Pallini, Attica.
Pharmathen is one of the largest private investors in research and development in Greece, with steady investments of 35 million annually in the Ramp;D sector and employs over1,350 peoplefrom over24 different nationalities. The company's enduring success is attributed to the passion for creativity, the ethics, and dedication of its people, who share the company's vision of making a difference in people’s lives.
Due to continuous growth and expansion,Pharmathen Pharmaceuticalsoffers a great opportunity for career development and is seeking to recruit aFinal Products Reviewer at ourSapes premises.
As aFinal Products Reviewer you will review Quality Control related documents in order to ensure proper compliance with established Quality Specifications.
More particularly:
What you will do:
- Follow Company's Quality Policy and complies with current operational standards and legislative requirements
- Works in accordance with the requirements of the written Policies, Standard Operating Procedures, Technical Directives and Protocols of the company's Quality System, that are related to the duties of the described position
- Follow the rules of hygiene and control of health status as defined in the relevant Policies and Standard Operating Procedures
- Maintain Quality Systems covering: document control, specifications, SOP’s,and regulatory documents
- Create, maintains, and updates COA/COC and Specifications
- Maintain new Batch/Fill Specs instructions for pre-weigh, blending, filling, and packaging activities
- Maintain Change Control, ERP system and Batch/Fill Specs database
- Review Batch/Fill Cards for proper compliance with established specifications
Requirements
The ideal candidate should have:
- Minimum an BSc Degree in Chemistry or relevant field
- At least 2 years of experience in a similar role
- Experience in a GMP or GLP environment
Job-Specific Skills:
- Excellent communication in English language (writing amp; speaking)
- Excellent knowledge of MS Office
- Good Technical Writing ability
- GMP/GLP and biopharmaceuticals experience preferred
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.