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Republic of Ireland
Republic of Ireland
Quality Technician
Dublin
Dublin
Packaging Engineer
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Recruitment Consultant
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Associate Global Trade Ops
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Senior Electrical Engineer
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R&D Director
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Engineering Business Manager
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Clean Utilities Engineer
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Senior R&D Project Manager
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Senior Project Manager - Process Develop
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Digital Lab Records Specialist
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Principal Process Equipment Engineer
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Senior EHS Specialist
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Senior Manufacting Engineer
Republic of Ireland
Republic of Ireland
QC Analyst
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Process Engineer
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Carlow
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Senior R&D Engineer
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Technical Transfer Specialist - Remote
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Senior Technical Writer
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Associate Quality Specialist
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Manager/ Senior Manager Drug Product Man
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Senior Associate Quality Control
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Quality Manager
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Principal R&D Engineer
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Project Manager
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Senior R&D Engineer
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R&D Manager
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Maintenance Planner
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Senior Quality Engineer
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Galway
Apply for this job
Details
Process Support Specialist
Reference: | SMC3596 | Location: |
Carlow |
Qualification: | Degree | Experience: | See description |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
QA Analyst
We’re currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Carlow. 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
- Be a document system expert; this will include document review, approval and document system work flow expedition. 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, and change controls.
- Support operation activities through documentation generation, filing, tracking, auditing and efficient maintenance of all associated databases including the maintenance, auditing and archiving of the process documentation system.
- Support Batch release through timely Quality Notification completion, Interim/summary report generation; meeting batch release requirements.
- Raise CAPA's and conduct investigations. Raise and investigate quality notifications using standard tools and methods, to resolve system issues e.g. FMEA, Fishbone diagrams, 5 why’s etc.; implement subsequent corrective action through the change management system.
- Complete Customer complaint investigations and Change Controls and ensure they are closed out to support production activities in a timely manner in conjunction with the SCM team.
- Required to comply with Merck 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.
Education & Experience
- Bachelor’s Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
- SAP knowledge and experience required
- Report, standards, policy writing skills required
- Equipment and process validation
- Sterile filling processes and equipment
- Lean Six Sigma Methodology experience desired
If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 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
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