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Senior QC 24/7 Shift
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Dublin
Quality Manager / PRRC
Dublin
Dublin
Biomedical Engineer
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Dublin
Injection Moulding Engineer
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Senior Project Engineer
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Carlow
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Quality Engineer
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Republic of Ireland
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R&D Engineer
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Galway
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Galway
Senior Validation Engineer
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Project Manager - R&D
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CQV Lead
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Process Engineer
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Carlow
NPI Process Engineer
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Carlow
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Greece
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Senior R&D Engineer
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Associate Quality Specialist
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Tipperary
Lead Maintenance Reliability Engineer
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Westmeath
Manufacturing Engineer
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Wexford
Senior Electronic Engineer
Dublin
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Senior Design Engineer
Dublin
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Senior Quality Engineer
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Quality Assurance Engineer
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Project Engineer
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Limerick
Lead Project Engineer
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Carlow
Product Development Engineer
Dublin
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Applications Scientist
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Engineering Business Manager
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Dublin
Recruitment Consultant
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Republic of Ireland
NPI Process Engineer
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Carlow
R&D Manager
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Galway
Manufacturing Technician
Clare
Clare
Senior Engineering Manager
Limerick
Limerick
Maintenance Engineer
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Carlow
Manufacturing Technician
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Clare
Electrical Engineer
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Tipperary
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Process Development Engineer
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Senior R&D Engineer
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Galway
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Clare
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Program Manager
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R&D Program Manager
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Senior R&D Engineer
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R&D Manager
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Business Manager (Pharma Chemicals)
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Senior Manufacting Engineer
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Republic of Ireland
R&D Manager
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Connaught
Apply for this job
Details
C&Q Lead
Reference: | SMC3785 | Location: |
Tipperary |
Qualification: | Degree | Experience: | See description |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Engineering Manager
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.
Duties
- Manage team of C&Q Engineers on high profile client site throughout the project lifecycle.
- Delta-V experience is desirable, running EM’s and CMs.
- API experience required
- Strong trouble shooting experience
- Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required.
- Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements.
- Investigate and resolve technical issues with assistance from engineers and/or suppliers.
- Ensure site project execution is undertaken in compliance with company guideline, department procedures and safety standards.
- Be familiar with the Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up).
- Schedule preparation and progress review.
- Organize and review daily activities of other CQV Engineers assigned to the project.
- Project management principles to coordinate CQV activities and reporting to Company and Clients PM.
- Contractors and Vendors management and coordination.
- Final Handover reports to the Client users
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