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Apply for this job
Details
CQV Lead
Reference: | SMC3895 | Location: |
Tipperary |
Qualification: | Degree | Experience: | Graduate |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Validation Coordinator
We’re currently recruiting for an exciting opportunity with a 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
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