Project Engineer
at Wood Group Pratt Whitney Industrial Turbine Services LLC
Ware, England, United Kingdom -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 02 Jun, 2024 | Not Specified | 02 Mar, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
| Citizen | GC |
| US Citizen | Student Visa |
| H1B | CPT |
| OPT | H4 Spouse of H1B |
| GC Green Card |
Employment Type:
| Full Time | Part Time |
| Permanent | Independent - 1099 |
| Contract – W2 | C2H Independent |
| C2H W2 | Contract – Corp 2 Corp |
| Contract to Hire – Corp 2 Corp |
Description:
Wood Process & Energy is recruiting a Project Engineer to join us on a Staff basis.
The role will be based on a client site in Ware and would welcome applications from candidates with a strong background in Pharmaceuticals or FMCG.
You will be supporting the CapEx delivery of equipment and facilities on a site undergoing consistent and varied investment.
WHO WE ARE LOOKING FOR:
- HND / HNC in a relevant Engineering discipline
- Good knowledge of GMP within a Pharmaceutical Environment
- Advanced knowledge of the following:
- Facility Validation
- Equipment Validation
- Demonstrable experience in the management of multi disciplined pharmaceutical projects or other relevant industries is strongly preferred
- Excellent communications skills
- Strong effective delegation skillsExposure to working within a technical environment
Responsibilities:
- Organise validation activities to provide an effective validation service.
- Present & justify validation scope and documents
- Review and approve documentation and reports supporting the validation exercise
- Ensure that both team and key stakeholders are kept informed of changes to validation requirements
- Plan validation activities to ensure customer and business needs are met in alignment with the overall project plans and objectives
- Conduct formal GMP reviews during the concept, scheme and detailed design phases
- Risk Assessment for GMP Systems
- Design Qualification (with Traceability Matrix) for GxP Systems
- Review of FAT protocols and FAT witness
- Review of Vendors’ SAT protocols
- Preparation of Commissioning protocols for installed systems
- Preparation and execution of IQ/OQ protocols for validated systems
- Raising and co-ordinating engineering change controls for equipment and facility modifications
- Review of IQ/OQ protocols prepared by equipment Vendors
- Coordination/witness to SAT/Commissioning tests executed by Vendors/Contractors
- Review of executed SAT/Commissioning protocols
- Coordination/witness/execute IQ/OQ tests by/with Vendors/Contractors
- Review of the executed IQ/OQ protocolsWork in conjunction with the QA Validation Leader to get documents approved promptl
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Electrical/Electronic Manufacturing
Site Engineering / Project Management
Electrical
Graduate
Proficient
1
Ware, United Kingdom
