Find a Job
237 available
Back to all search results

Quality Assurance Officer

Ref: 9222628

  • €30,000 - €35,000
  • 26 Apr 2021
  • Tipperary
  • Perm

This is an excellent opportunity for an ambitious Quality Assurance Officer to join an expanding company and work on the start up of it's newest facility. On offer is a dynamic and growth oriented environment with progression opportunities along with a competitive salary and benefits package.

About the Job:

  • Co-ordinate and lead activities to close-out corrective/preventive actions.
  • Support the Laboratory Team in management of equipment and equipment records.
  • Take ownership of the Pharma change control procedure, ensuring that assigned tasks are completed to the scheduled timelines.
  • Management of the CAPA process within the Pharma Laboratory.
  • Ensure that all methods and procedures held by the laboratories are current
  • Regularly update trending systems for Right First Time (RFT) data generated by the laboratory
  • Support the Laboratory Team to ensure that training records are maintained
  • Support the Laboratory Team in management of External and Internal Quality Control samples including maintenance of the in-house IQC reference material
  • Assist the Laboratory Team during customer and regulatory visits/audits
  • Control and archiving of laboratory records
  • Support the Laboratory Team to ensure that all relevant Health and Safety information is included on Client provided methods
  • Ensure all Quality requirements are met and delivered on time and review procedures and systems regularly for continuous improvement
  • To provide the Laboratory Team with updates and reports upon request
  • Lead Pharma laboratory routine audit trail reviews and prepare reports in line with current regulatory requirements
  • About You:

  • A scientific background (degree level) preferably in Chemistry
  • An understanding of Quality Management Systems, INAB/UKAS and GMP requirements and the knowledge to drive change within the Pharma Laboratory
  • 2+ years experience working in a GMP environment
  • The ability to work on your own and manage projects to tight deadlines
  • Excellent communication and interpersonal skills
  • Ability to influence opinion and set standards
  • Understanding of the Pharmaceutical Industry and clients’ needs
  • Good computer literacy skills
  • High level of reporting and writing skills
  • Excellent organisational skills and the ability to multi-task
  • High attention to detail and a methodical approach
  • For more on the role call Nigel on 087 3618142 or send your CV for consideration.