Quality Assurance Junior Officer
Pharmathen, Greece
Job Description
We are one of the leading complex drug delivery and formulation developers, using our key in-house technologies to support improved patient compliance. We service a broad partner network of over 250 customers in over 90 countries throughout Europe, North America, South America, Middle East, Asia, Australia and Southern Africa.
Our portfolio consists of over 100 products, and today we are working on one of the most extensive and advanced pipelines in Long Acting Injectables, Sustained Release formulations and Preservative Free Ophthalmics, produced in our in-house US-FDA and EU-approved facilities.
We proudly employ more than 1,200 people from over 22 different nationalities across 9 locations. We welcome the opportunity to expand our collaboration with existing partners as well as to establish new partnerships, while remaining committed to our vision to make a difference in people’s lives through our everyday activities and our products.
Due to continuous growth and expansion, Pharmathen offers a great opportunity for career development and is seeking to recruit a Quality Assurance Junior Officer to join our Quality Assurance team at our Sapes, Rodopi premises.
As a Quality Assurance Junior Officer, the ideal candidate will be responsible for ensuring compliance with GMP requirements and ISO standards.
More particularly:
What you’ll do:
- Handle the technical implementation of GMP requirements
- Participate in the preparation and review of Standard Operating Procedures, Technical Directives, and of the rest of controlled documents of the Quality System of the company
- Support in the issuance of Standard Operating Procedures, Technical Directives and of the rest of controlled documents of the Quality System of the company
- Ensure compliance of corporate processes to GMP requirements
- Handle corporate quality management system’s documentation and records
- Support in compliance processes such as Audits (Internal/External), Inspections, etc.
- Support in product/site registrations
- Control production and packaging Technical Directives
Requirements
The ideal candidate should have:
- BSc in Chemistry, Biology, Pharmacy, Engineering or equivalent
- Experience within a manufacturing unit / laboratory / Quality unit operating under GMP / GLP / ISO or other regulatory standards
- 1 - 2 years of experience in Quality Assurance in Pharmaceutical Industry will be considered an asset
- Fluency in English language (writing amp; speaking)
- Computer literacy
- Ability to prioritize tasks and meet deadlines
- Exceptional communication skills, strong project management skill
Job-Specific Skills:
- Fluency in English language (writing amp; 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.
Submit your application no later than the 03/08/2022.