Quality Assurance Supervisor -Pharmaceutical&Medical- Mirandola

Location
Modena
Salary
Negotiable
Posted
Aug 07, 2017
Closes
Sep 06, 2017
Ref
53217
Contact
Valerio Celenza
Jobseeker Type
Professional
Organization Type
Corporate
Contract Type
Employee
Hours
Full Time

My client is a well renowned manufacturer part of a Multinational group. Due to its renovation they are currently looking for a Site QA Supervisor to straighten their Production site in Mantova.

With their advanced sterilisation services, company has created a network in more than 50 different locations which will allow you to work for a well-established business also having a strong international exposure.

The Site QA Supervisor will be the main responsible for all quality matters relating to the operations on the site assigned under the supervision of the Country Quality Manager.

Principal Duties and Responsibilities:

  • To review batch documentation after processing and to ensure that errors problems and anomalies are fully investigated and documented
  • To be responsible for product release for all processing at site.

  • To initiate, investigate, control and analyse non-conformance reports ensuring all relevant parties are informed and where appropriate, to ensure corrective action, in collaboration with all departments involved, is implemented and that it is effective

  • To be responsible for the Quality and GMP training of all site personnel. To develop, support and maintain the Production Employee Training Program about Quality Guidelines in collaboration with Country Quality Manager
  • To facilitate Audits (Regulatory Inspections, Audits by Customers, audit to Supplier) in collaboration with Country Quality Manager. Ensure that the internal audit program is executed as per plan and perform audits as required.

Requirements and Skills:


  • Degree in a science (pharmacy, CTF, biology, biotechnology, Bio-medical engineering, chemistry)
  • Minimum 3 years of experience in Production/QA activities in Pharmaceutical/Chemical/Medical Industries
  • Preferable and appreciable knowledge in ISO 13485, GMP and quality management
  • High level of English reading, writing and speaking communication skills
  • Maintain good relationships with the Production and QA team, co-workers and all departments
  • Full availability to travel

  • For a confidential discussion, or to apply, send your CV to me, v.celenza@nonstop-devices.ch.

    NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Pleas