FAMAR is a European contract manufacturing and development partner for the pharmaceutical and health & beauty industry. Building on our 70 years’ expertise, we deliver flexible solutions, from development to production and distribution. Driven by our customer-care mindset, we offer services covering the majority of pharmaceutical forms, while providing a particularly strong expertise in Liquids, Ointments and Creams. Through the outstanding knowledge and commitment of our 1850 employees and with a network of 6 production sites, we supply a wide range of 1800 products in 125 international markets.
We seek to recruit a Quality Contracts Officer.
QUALITY CONTRACTS OFFICER
(QCO_1.2023)
About the Role:
The position holder will be required to:
Coordinate all Legal Quality Contracts program at Group level, ensuring consistency with Company Strategy, Group Quality requirements, commitments and goals.
Contribute to the development and improvement of the quality system documentation.
Location:The position can be at any location in Greece, where the FAMAR Group Quality Function has presence: Alimos, Anthoussa or Avlona.
Main Responsibilities:
Coordinate the review of the Legal Quality Contracts, including QP-QP Agreements, SDEAs and Supplier and Service Provider Quality Agreements.
Coordinate the review of the commercial and service level agreements with the Quality Unit of the sites.
Maintain the Legal Quality Contracts mapping including the QP-QP agreements.
Monitor and report the Group Legal Quality Contract KPIs.
Keep up-to-date the Legal Quality Contracts documentation repository.
Profile, Skills, Qualifications:
General Requirements:
University Degree of scientific background in Chemistry/Chemical Engineering/Pharmacy/Biology (Postgraduate studies preferred).
2 years of pharmaceutical industry experience, including 1 year in quality compliance roles.
Excellent verbal and written knowledge of the English language. Fluency in other languages (e.g Spanish, Italian or Greek) will be considered an advantage.
Strong written and verbal communications and presentation skills.
Strong project management skills (planning, prioritization, problem solving and follow up).
Strong organizational and time management skills needed to manage multiple ongoing projects simultaneously and the ability to analyze and problem solve.
Ability to work across cultures/countries/sites at high quality standard and possess high level of attention to detail.
Advanced PC skills: excellent MS Office knowledge - Word, Excel, PowerPoint.
Technical Qualifications:
Experienced with electronic management platforms eQMS.
Advanced knowledge of EMA GMP legislation and associated pharma industry guidelines (ICH, PICs, WHO, etc.).
Knowledge of FDA guidelines.
Knowledge of Quality Management Systems and requirements of other categories of products e.g. medical devices, cosmetics etc.
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