QA Product Support
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards. You will achieve, together with your colleagues in Quality Assurance, Quality Control, Regulatory and Quality Systems, the delivery of a resilient supply of quality products to our clients.
This opportunity is for a QA product specialist to join the Quality Assurance Team for a fixed term contract with an immediate start.
Your Responsibilities

You will:

• Reporting directly to the Quality Assurance Manager, ensures the Batch record review for fermentation, utilities, finished products and intermediates. Coordinates the investigation of product quality concerns (Deviations, OOS and OOT) and the follow up of the related CAPAs. Support the investigation and CAPAs definition of complaints. Checks the content of the “Master Batch Production Records” and Operating Manuals and the compliance with the good manufacturing standards, site procedures, technical documentation filed and approved by the relevant Health Authorities, HSE and company policies and directives
• Support the preparation of Product Quality Reviews (PQR’s); monitors the corrective and preventive actions (CAPA) for continuous improvement of the quality of production, packaging and processes robustness
• Support the preparation of inspection visits (Regulatory Authorities, Customers). Participates in inspection visits and contributes to the implementation of any corrective actions
• Support the conduction of programs related to the compliance of the Good Manufacturing Practices (GMP)
• Disseminates the Quality culture in the production departments providing the necessary specialist assistance for the implementation of specific programs of processes and performances improvement.

EUROAPI is focused on reinventing active ingredient solutions to sustainably meet customers’ and patients’ needs around the world. We are a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio, offering a large span of technologies, while developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities.
Taking action for health by enabling access to essential therapies inspires our 3,450 people every day. With strong research and development capabilities and six manufacturing sites all located in Europe (Saint-Aubin-lès-Elbeuf and Vertolaye in France, Brindisi in Italy, Frankfurt in Germany, Budapest in Hungary and Haverhill in the UK), EUROAPI ensures API manufacturing of the highest quality to supply customers in more than 80 countries.
EUROAPI is listed on Euronext Paris.
The EUROAPI Italy facility is a vast production site with over 240 workers located in the industrial area of Brindisi with a history dating back to 1966. EUROAPI Italy is specialized in the development and manufacturing of Active Pharmaceutical Ingredients (APIs), including antibiotics, corticosteroids and other intermediates by large scale fermentation under GMP conditions. The Brindisi site is approved by the main health authorities and owns environment and workplace safety certifications.

Our Requirements

• Scientific degree: degree in Biotechnology, CTF, Chemistry, Biochemistry Previous experience in QA, QC and/or Fermentation Plants
• Consolidated experience in cGMP pharmaceutical environment
• Good knowledge of cGMP application
• Knowledge of the Office package
• Knowledge of IT tools used in pharmaceutical environment for the management of GxP activities (i.e. SAP)
• Knowledge of English at least medium level: both spoken and written.
• Motivation and sensitivity towards all aspects relating to Good Manufacturing Standards
• Ability to work in team and to establish open and collaborative human relationship
• High determination on results achievement and target accomplishment
• Flexibility and strong adaptability

Your Benefits

• Competitive Salary
• Annual Bonus
• Training & Development
• Company canteen

Culture & Values at EUROAPI
We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognize that how we do things is as important as what we do, and our values set out how we achieve our goals and help us “do it right”.
Diversity & Inclusion
EUROAPI is committed to nurturing a culture of diversity and inclusion that contributes to improving innovation, performance, and engagement. We value transparency, mutual respect, and equal treatment of people. For this reason, we are firm in protecting our employees against any forms of discrimination.
Environment, Social and Governance
We strongly believe that the success of our company lies in its capacity to adapt to tomorrow’s challenges. Our responsibility as a company is to provide sustainability and resilience to the pharmaceutical value chain.
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Please refer the Job description for details