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Job Description
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 or for further information.
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