About the Company
A Global Healthcare company is looking for a Lead Manufacturing Associate to join their new state of the art facility in Meath on a 11-month contract due to continued growth and expansion. You will be responsible for supporting the manufacturing process, while ensuring objectives are effectively achieved.
About your new job as a Lead Manufacturing Associate
- Identify, escalate, and address compliance, safety, and process deviations.
- Support safety audits, inspections, risk assessments, and corrective actions.
- Assist in incident investigations and implement improvement actions.
- Provide coaching on the shop floor to prevent issues.
- Participate in cross-functional teams to drive projects and goals.
- Lead projects and continuous improvement initiatives aligned with site strategies.
- Manage document accuracy and support continuous improvement frameworks.
- Support compliance and operational efficiency initiatives.
- Lead handover meetings and provide updates to shift leads.
- Act as point of contact for troubleshooting, problem-solving, and issue resolution.
- Oversee suite activities and cover for the shift lead as needed.
- Ensure equipment maintenance, troubleshooting, and repairs for smooth operations.
- Manage equipment shutdowns and ensure resource availability to reduce downtime.
- Perform and assist with operations to fulfil assigned responsibilities.
- Implement shift standard work to promote a team-based approach for batch progression.
- Conduct sampling and in-process testing to support manufacturing and validation processes.
- Accurately document activities to ensure accountability and traceability of production records, following the Right First Time (RFT) principle.
- Author, review, and edit procedures and technical documents to ensure compliance with cGMP standards.
- Provide coaching to shift teams on the RFT approach for accurate documentation.
- Ensure all tasks related to manufacturing documentation support adhere to good manufacturing practices (GMP).
What skill/experience you need as a Lead Manufacturing Associate
- Bachelor’s degree in science, Engineering or other technical discipline.
- Minimum 5 years’ experience in a regulated GMP environment.
- 3 years’ experience in Biopharma industry, with direct experience of biologics manufacture would be desirable.
What’s on Offer
- Attractive hourly rate DOE
- Shift Allowance at 33.3%
- Enjoy a supportive work environment with a focus on maintaining a healthy work-life balance.
What’s Next
Apply now by clicking the "Apply Now" button or call Elaine McCarthy at +353 21 4847135. If this job isn’t quite right but you’re looking for something similar, please get in touch. We also have multiple temporary, FTC, and contract jobs available.
