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Senior Quality Engineer
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Dublin
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Clare
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Apply for this job
Details
Compliance Engineer
Reference: | RK22831 | Location: |
Carlow |
Qualification: | Degree | Experience: | 3-4 Years |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Compliance Specialist
Compliance Engineer
RK22831
Contract – 11 months
Carlow
Hybrid
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Tipperary. 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 role will be responsible for supporting the Engineering Department in a GMP and Sterile Environment. Ensure that objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers.
Duties:
- Direct and/lead deviations, out of tolerance conditions and unexpected results, conducting failure
- analysis, root cause determination and implementing corrective actions.
- Preparation and analysis of Engineering metrics reports to trend for improved operational efficiencies.
- Format, write, deliver and review necessary documentation in line with the standard approval process, and facilitate others to do so. Documents will include SOP’s, SWI’s, training documents, JSA’s, PM's and change controls.
- Accountable for leading investigation analysis, identifying true root cause, identifying gaps and actions to close gaps. Collaborate with Engineering colleagues and other departments particularly IPT, Quality, EHS,
- Technical Engineering in completion of tasks.
- Required to comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
- Work collaboratively to drive a safe and compliant culture in Carlow.
- May be required to perform other duties as assigned
- Support Audit Readiness activities
Experience and Education:
- Third Level Degree qualified in a Science/Engineering or related discipline.
- 3-5 years prior related work experience ideally in a manufacturing, preferably GMP setting.
- GMP Audit experience in the pharmaceutical industry
- Experience with documentation such as SOP’s, SWI’s, training documents, JSA’s, PM's and change controls
If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.
Pharmaceutical Quality Control Biopharmaceutical Diagnostics Chemistry Sales and Marketing Microbiology Packaging Engineer Medical Device Dublin IT Connected Health Project Manager Sales and Marketing Pharma Sales Quality Assurance PhD Medical Affairs Cork Manufacturing Executive Allied Healthcare Supply Chain Life Science Clinical Research Scientist Academic Mayo Limerick Supply Chain Academic Scientific Biotechnology Engineering Validation Engineer Laboratory Scientist Quality Engineering Cork City Product Development Engineer
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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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