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CQV Engineer (Clean Utilities)
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Dublin South
Project Engineer
Clare
Clare
Production Operator
Carlow
Carlow
Recruitment Consultant
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Injection Moulding Engineer
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R&D Director
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Senior R&D Engineer
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Galway
R&D Manager
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Maintenance Planner
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Senior QC Associate
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E&I Turnover Engineer
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R&D Project Manager
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Senior R&D Engineer
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QA Operations Specialist
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Galway
Senior R&D Engineer
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Quality Validation Engineer
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R&D Program Manager
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Senior Regulatory Affairs
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Carlow
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Principal R&D Engineer
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Principal R&D Engineer
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Compliance Specialist
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R&D Manager
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R&D Director
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Remote Process Engineer - Fill Finish
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Account Manager UK and Ireland
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Senior Equipment Engineer
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Senior Operations Engineer
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Senior R&D Manager
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Athlone
Compliance Specialist
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Carlow
Senior R&D Engineer
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Business Manager (Pharma Chemicals)
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Apply for this job
Details
Quality Operations Specialist
Reference: | RK1999 | Location: |
Louth |
Qualification: | Degree | Experience: | 4-5 Years |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
QA Specialist
Quality Specialist (Manufacturing Oversight)
Contract – 6 months
Dundalk
We’re currently recruiting for an exciting project opportunity with a pharmaceutical manufacturing facility based in Dundalk.
We are looking for QA Specialists who are committed to enhancing product quality, reducing compliance risks, and improving regulatory audit readiness.
Key Responsibilities:
- Provide comprehensive oversight of the OSD filling line setup, operation, line clearance, and cleaning processes.
- Ensure all manufacturing operations adhere to standardized protocols for efficiency and compliance.
- Conduct routine inspections and batch record reviews to verify compliance with regulatory standards.
- Lead the investigation of deviations, implementing corrective and preventive actions (CAPAs) to ensure timely resolution, mitigate risks and prevent recurrence.
- Implement change controls, ensuring seamless integration of changes with minimal impact on production.
- Conduct training sessions for manufacturing staff to reinforce best practices, compliance, and efficiency in operations.
- Collaborate with a team committed to efficiency and teamwork, contributing to reduced downtime, increased throughput, and the maintenance of high-quality standards.
Requirements:
- Proven experience in the pharmaceutical industry (5+ years), with hands-on experience in manufacturing operations
- Strong understanding of quality assurance processes, including deviations, CAPAs, and change control management.
- Oral Solid dose experience (desired)
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.
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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
Valid XHTML - CSS