Project Engineer

LSC, Life Science Consultants; Limerick; On-site; EUR 60,000 - 80,000; Full time

Job summary

LSC, Life Science Consultants in Limerick is seeking a Project Engineer for a contract role within a GMP medical device environment. You will manage small to medium projects, support validations, and work with ISO safety standards to ensure compliance.

Ideal candidates have 2–4 years in life sciences, exposure to URS and MS Project, and experience in process development. Visa eligibility (Stamp 1G/Stamp 4) is required.

Qualifications

• Experience in GMP or medical device manufacturing.
• Experience in equipment and process validation activities.
• Process development experience.
• Familiar with ISO safety standards.

Responsibilities

• 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.
• Support and/or develop and execute equipment or process related validations in accordance with IML requirements, processes and procedures.
• Utilize necessary project tools, i.e. URS, Microsoft Project, etc. to manage projects successfully.
• Define root cause and implement solutions to equipment and process related non-conformances utilising the NCMR and CAPA processes

Skills

GMP/Medical devices

Validation

Process development

ISO safety

Tools

URS

Microsoft Project

Job description

Project Engineer – Contract Opportunity

LSC have a great contract opportunity for a Project Engineer to work in a medical device company in Limerick.

If you have 2-4 years of experience working in the life sciences industry and are ready for your next challenge, this could be the perfect opportunity for you!

ABOUT THE PROJECT – KEY RESPONSIBILITIES

• 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


• Support and/or develop and execute equipment or process related validations in accordance with IML requirements, processes and procedures


• Utilize necessary project tools, i.e. URS, Microsoft Project, etc. to manage projects successfully


• Define root cause and implement solutions to equipment and process related non-conformances utilising the NCMR and CAPA processes

ABOUT YOU – ARE YOUR SKILLS A MATCH?

• Prior experience in a GMP or medical device manufacturing environment


• Prior experience in equipment and process validation activities


• Process development experience


• Familiar with ISO safety standards

Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!