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Details
QA Specialist
Reference: | RK9352 | Location: |
Cork |
Qualification: | Degree | Experience: | 3-4 Years |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
QA Specialist
QA Specialist
RK9352
Contract – 12 months
Cork
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification, Annual product review and Validation compliance activities.
Duties:
- Batch Record Review & material release to ensure compliance with GMP requirements.
- Carries out tasks related to the administration of event management systems including Review & Approval of Event, Deviations, and Customer complaints.
- Carries out tasks related to the management of batch records design and approval.
- Carries out administration of the SAP Quality Management Module.
- Carries out tasks relating to the management of site change control systems.
- Compiles Annual Product Reviews.
- Supports all validation activities on site as described in the Site Validation Master Plan.
- Approves and compiles where appropriate validation protocols and reports (analytical, cleaning, computer, process, equipment, etc.).
- Supports system qualification and process validation activities.
- Reviews and approves SOPs/work instructions/forms from other departments on behalf of Quality Assurance
- Co-ordinates and assists in the preparation for regulatory and customer GMP inspections of the site.
- Participates in the introduction of new process or modified process steps, as part of a New Product Introduction Team (NPI)
- Perform GMP audits on-site and vendor facilities as required.
- Performs on the floor walkdowns regularly to ensure process and facilities are maintained to GMP standards.
- Carries out tasks related to the administration of site supplier approval process.
Experience and Education:
- Bachelors Degree in a scientific/technical discipline required
- 3-5 years’ experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry.
- Experience in auditing of external suppliers, contractors and vendors
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.
Supply Chain Cork Pharmaceutical Supply Chain Laboratory Scientist Scientific Diagnostics Biotechnology Biopharmaceutical Mayo Limerick Sales and Marketing Project Manager Medical Affairs Chemistry Sales and Marketing Dublin Product Development Engineer IT Scientist Quality Control Pharma Sales Quality Engineering Allied Healthcare Academic Microbiology Connected Health PhD Cork City Quality Assurance Academic Engineering Medical Device Packaging Engineer Validation Engineer Life Science Clinical Research Manufacturing Executive
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
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