- Planning, coordinating, and implementing projects related activities including Contracts, Commercial / Financial, Vendor and Client relationships, H&S, Quality, Procurement etc
- Working across multi-functional teams and working as a project liaison for vendor and client
- Perform DQ, IQ, OQ, PQ, and leading FAT's, SAT's, URS, GMP reviews, Risk Assessments, Change Controls, and regulatory audits
- Leading CQV (Commissioning, Qualification, and Validation) of Pharma and Packaging Equipment, as well as Utilities
- Managing capex and installation, commissioning, and qualification of equipment, machinery, resources, and other project related activities are carried out efficiently and to deadline
- Qualification in Engineering, or equivalent Manufacturing experience across Pharma, Medical Devices, Biotech, Packaging, or Food/FMCG
- Ideally between 3-5 years of working in relevant project, process, manufacturing or validation role or alternatively having worked long term fulfilling a similar role.
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Project Validation Engineer - United Kingdom - SRG
Description
Job title: Project Validation Engineer
Are you an Engineer with Project and Validation experience working within a highly regulated environment? An opportunity has arisen for an experienced Project Validation Engineer to join a manufacturing organisation in Yorkshire region.
About the Job:
In this role, you will work in a project facing role, coordinating, budgeting, and managing Pharma projects, as well as supporting the execution of IQ, OQ, PQ, FAT's and SAT's for a production and packing line, Utilities, and Manufacturing Equipment. The salary for this role is highly competitive and comes with excellent benefits.
Summarised responsibilities:
About you:
Please apply or contact me directly on
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
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