Our client, an established multinational in Cork, are seeking a Quality Engineer to join their team. They will consider anyone from a devices, Pharma or Biotech background.
Reporting to the Quality Manager, the Quality Engineer manages the technical quality aspects for their respective areas working closely with the Production personnel
Investigate Quality problems associated with the production department and implement effective corrective and preventive measures
Perform validations as required
Maintains control of changes on site ensuring compliance to relevant procedures and regulatory guidance/industry standard.
Oversees/Release of in-process and finished product ensuring compliance to specification.
Apply GMP and observe that it is being adhered to in the department.
Monitors, maintains and promotes compliance to the quality system within the dept. including but not limited to documentation system, complaints, change control and deviations
Participate in teams to help make necessary improvements and changes to all process related issues in the production department
Identify and implement continuous improvements in conjunction with the operations team.
Liaise with Vendors and Customers on quality related issues, internal and external.
Support customer and regulatory compliance audits as necessary.
Responsible for ensuring compliance with all applicable Environment, Health and Safety legislation and adherence to site EHS procedures for area of responsibilities.
Third level qualification or relevant knowledge and industry experience;
2-3 years previous experience in a similar role is desirable (Pharma/Biopharma);
Good investigative and problem-solving skills;
Good Communication skills;
Experience of cGMP a distinct advantage.
Contact Brian Christensen on 01 6854747 or submit your CV to email@example.com for immediate consideration
If you would like further Information you can contact the recruiter directly:
Brian Christensen | Tel: +353 (0) 1 685 4747