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Senior R&D Engineer
Dublin
Dublin
Senior Quality Engineer
Dublin
Dublin
R&D Engineer
Galway
Galway
Senior R&D Engineer
Dublin
Dublin
Quality Manager
Dublin
Dublin
Quality Specialist
Clare
Clare
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Roscommon
Roscommon
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Galway
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Galway
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Galway
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Galway
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Dublin
Dublin
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Dublin
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Dublin
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Longford
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Dublin
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Carlow
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Dublin
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Dublin
Dublin
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Dublin
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Galway
Quality Engineer
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Athlone
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Galway
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Galway
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Clare
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Dublin
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Dublin
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Dublin
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Dublin
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Galway City
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Galway
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Galway
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Galway
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Athlone
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Republic of Ireland
Senior R&D Engineer
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Galway
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Dublin
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Clare
Clare
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Galway
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Clare
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Dublin
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Leitrim
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Limerick
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Limerick
Limerick
Learning Systems Lead
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Limerick
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Galway
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Dublin
Dublin
Principal Process Equipment Engineer
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Republic of Ireland
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Galway
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Dublin
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Galway
Galway
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Dublin
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Leitrim
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Galway
Galway
Tech Transfer Lead
Dublin
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Health & Safety Specialist
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Dublin
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Galway
R&D Manager
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Galway
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Dublin
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Dublin
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Republic of Ireland
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Clare
Clare
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Galway
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Dublin
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Clare
Clare
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Athlone
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R&D Director
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Biomedical Engineer
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Product Development Engineer
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Galway
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Galway
Process Development Engineer
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Details
Senior Quality Control Associate
| Reference: | AS3646 | Location: |
Dublin South |
| Qualification: | Degree | Experience: | See description |
| Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. 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.
Duties:
- Plan and perform analyses with great efficiency and accuracy.
- Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
- Report, evaluate, back-up/archive, trend and approve analytical data.
- Troubleshoot, solve problems and communicate with stakeholders.
- Initiate and/or implement changes in controlled documents.
- Participate in audits, initiatives and projects that may be departmental or organizational in scope.
- Review protocols and perform assay validation and equipment qualification/ verifications when required.
- Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
- May contribute to regulatory filings.
- May conduct lab investigations as necessary.
- Evaluate lab practices for compliance on a continuous basis.
- Approve lab results.
- May interact with outside resources.
- LIMS data coordination of commercial and import testing on site where applicable
- May represent the department/organization on various teams. May train others.
- Bachelor’s degree in a Science related field is required.
- 3+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry,
- Strong background in Chemistry and Analytical testing is required.
- Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
- Experience with analytical techniques such as Compendial testing would also be advantageous
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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
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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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