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Project Engineer (Pharmaceutical) / England
This job has expired or may no longer be taking applications, but other similar jobs are available.
Added: | 2024-02-16 |
Location: | North West North West England, England |
Salary: | |
Duration: | Contract |
Apjid | 3 |
Title: Project Engineer
Location: Northwest UK
Hourly rate: £50 - £60 p/hr
Start date: March / April 2024
Contract Length: 12 months
Looking for a Project Engineer to join a global pharmaceutical company based in the Northwest UK on a contract basis. This is a long term contract which is Inside of IR35.
This is a technical role focused on supporting key process improvement initiatives and major capital projects to meet strategic business performance targets (e.g. financial, supply chain, write-offs, cGMP & HSE).
Location: Northwest UK
Hourly rate: £50 - £60 p/hr
Start date: March / April 2024
Contract Length: 12 months
Looking for a Project Engineer to join a global pharmaceutical company based in the Northwest UK on a contract basis. This is a long term contract which is Inside of IR35.
This is a technical role focused on supporting key process improvement initiatives and major capital projects to meet strategic business performance targets (e.g. financial, supply chain, write-offs, cGMP & HSE).
- Responsible for creating accurate and timely cost estimates for projects in accordance with departmental procedures, to ensure that project proposals can be submitted for approval in line with the capital expenditure plan
- Lead complex engineering projects involving cross functional teams and multiple GMP disciplines (e.g. process / utilities / cleanrooms.
- Budget and schedule responsibility for multi-disciplinary GMP projects, including monitoring and reporting on the status of major projects in multiple formats including board reports and presentations
- Participate in the validation and handover processes for capital projects in liaison with quality assurance, production management and maintenance function, and ensure that all necessary training, drawings and documentation are provided for validation, operation and maintenance purposes
- Uphold and contribute to the development of site engineering standards to comply with regulatory and pharmaceutical industry requirements. Ensure that appropriate standards of GMP, housekeeping, safety and discipline are maintained at all times both within the department and operational areas.
How to Apply
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