- Makes decisions within guidelines and policies which impact own priorities and allocation of time to meet deadlines.
- Supports Corporate Quality to ensure actions related to Quality Systems and/or Operational Quality at the site are executed.
- Participation in inspections of Site by Divisional / Regulatory Bodies / third parties together with follow up actions where applicable.
- Ensure supply of high quality product through the implementation and oversight of the Quality Management System for the site.
- Ensure the highest Quality, Compliance and Safety standards.
- The Associate Specialist/ Specialist will participate and comply with the MMD Quality Management System (QMS) requirements, including ownership.
- 1 - 5 years' experience in the Pharmaceutical industry or a similar operating environment which includes experience in a Quality function
- Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation (i.e. Quality, science etc.)
- Operational experience of at least 4 QMSs
