Κωδικός Θέσης : QCO_1.2023
Ημερομηνία ανάρτησης αγγελίας : 23/1/2023

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.



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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