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Details
Project Engineer
| Reference: | AS26067 | Location: |
Limerick |
| Qualification: | Degree | Experience: | See description |
| Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Equipment Engineer, Project Engineer
We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Limerick. 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.
This position will be responsible for providing engineering support in developing new or improving existing equipment and/or process related activities. Define or assist in defining process equipment requirements and specifications based on process requirements, company’s safety requirements and customer needs.
Duties:
- Perform project management tasks for small to medium scale projects involving either new or existing equipment
- Assist in determining the budget to support requirements
- Evaluate or assist in evaluating technology necessary to support requirements
- Propose options to Management/Customer/Stakeholders
- Provide technical support for projects
- Support and/or develop and execute equipment or process related validations in accordance with IML requirements, processes and procedures
- Assist in negotiation with equipment suppliers
- Utilize necessary project tools, i.e. URS, Microsoft Project, etc. to manage projects successfully
- Develop the necessary equipment, process and product knowledge to be recognised as a local expert.
- Measure/evaluate equipment efficiencies, downtime and assist in the development of maintenance requirements
- Propose and implement improvement projects that improve compliance, improve efficiencies, yields or throughputs
- Define root cause and implement solutions to equipment and process related non-conformances utilising the NCMR and CAPA processes.
- Actively interfacing with cross-functional team members, always practicing good team work in support of day to day operating requirements
- Ensure effective closure on quality system documents (Audit Action, NCR’s, CAPA’s, Maps, etc.)
- Implementation of safety/environment requirements on purchase and changes of all new and existing equipment.
- Hold a relevant degree or equivalent qualification in production, manufacturing or mechanical engineering.
- 3 years’ minimum experience in a Manufacturing or Project Engineer role from a GMP regulated environment.
- Prior experience in equipment and process validation activities
- Process development experience
- Familiar with ISO safety standards
- Previous experience in the use of ‘black belt’ statistical techniques would be a distinct advantage, as would familiarity with equipment validation in a FDA environment
- Have statistical process control and capability analysis using ANOVA and DOE techniques
- Ability to apply a scientific approach to problem solving, blending analytical and experimental skills to maximize productivity and yields is an essential requirement.
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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
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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
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