Manufacturing Operator - Medical Devices (12-Month Contract)

Stryker; Limerick; Sur place; EUR 29 000 - 41 000; Plein temps

Résumé du poste

Stryker is seeking a Manufacturing Operator in Limerick to perform SOP-driven manufacturing, inspection and packaging of medical devices. You will work within a team to produce, package and label high quality products, and maintain accurate production records.

The role emphasizes adherence to GMP practices, safety, and line clearance. A Leaving Certificate or equivalent education is required, with experience in regulated manufacturing being an advantage.

Qualifications

• Leaving Certificate, Trade or equivalent education level is required.
• Experience in a regulated manufacturing environment is an advantage.
• Capable of working as part of a multi-disciplined team.
• Good Communication Skills.
• Experience in GMP environment is preferred but not essential.
• This role is initially a 12 month fixed term contract for our Limerick site.

Responsabilités

• Producing and/or packaging and labeling high quality product within a team environment, in line with standard operating procedures.
• Inspecting components by using precision measuring equipment to ensure components meet engineering specifications.
• Completing production records and maintenance logs.
• Maintaining a high standard of housekeeping.
• Adhering to all Health and Safety procedures and requirements.
• Final Inspection Activities to include finished goods inspection and DHR review.
• Demonstrating safe working practices, correct use of equipment, product verification and the adherence to EHS, line clearance and 5 pillars compliance.

Connaissances

Team player

Good communication skills

Reliable

Formation

Leaving Certificate/Trade or equivalent

Description du poste

Stryker is seeking a Manufacturing Operator in Limerick to perform SOP-driven manufacturing, inspection and packaging of medical devices. You will work within a team to produce, package and label high quality products, and maintain accurate production records.

The role emphasizes adherence to GMP practices, safety, and line clearance. A Leaving Certificate or equivalent education is required, with experience in regulated manufacturing being an advantage.