Project Engineer

LSC, Life Science Consultants; Limerick; On-site; EUR 45,000 - 65,000; Full time

Job summary

LSC, Life Science Consultants in Limerick is seeking a Project Engineer for a contract role. You will manage small to medium scale projects involving new or existing equipment and support validation activities in a GMP medical device environment.

Ideal candidates have 2-4 years in life sciences, experience with equipment/process validation, and familiarity with ISO safety standards. A Stamp 1G/Stamp 4 visa is required to apply for this contract opportunity.

Qualifications

• 2-4 years experience in life sciences industry preferred.
• Experience in GMP or medical device manufacturing environment required.
• Experience performing equipment and process validations.
• Familiar with ISO safety standards and related procedures.

Responsibilities

• Perform project management tasks for small to medium scale projects involving new or existing equipment.
• Assist in determining the budget to support requirements.
• Evaluate technology to support requirements.
• Support equipment or process related validations per IML requirements.

Skills

GMP environment

Medical device manufacturing

Equipment validation

Process validation

Job description

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!