Manufacturing Associate (m/f/x)*

IRL KCI Manufacturing Unlimited Company; Athlone; On-site; EUR 35,000 - 45,000; Full time

Job summary

IRL KCI Manufacturing Unlimited Company in Athlone, Ireland is seeking a Manufacturing Associate to carry out a range of manufacturing activities. This role ensures the achievement of GMP standards of quality, cost, and service within the manufacturing operation.

The ideal candidate will have at least 2 years of experience in a medical device or similar industry and possess good communication skills and strong teamwork abilities. This position requires a commitment to manufacturing excellence and compliance with all relevant standards and procedures.

Qualifications

• Minimum 2 years experience in medical device or similar industry.
• Established track record in manufacturing processes.
• Ability to follow G.M.P. procedures and policies.

Responsibilities

• Complete manufacturing work-steps under supervision.
• Verify quality of products at each work-step.
• Maintain raw material levels with Kanbans.

Skills

Manufacturing activities

Good verbal and written communication skills

Strong teamwork abilities

Commitment to achievement of manufacturing excellence

Flexibility

Education

2nd Level education or equivalent

Job description

Job Overview

As a Manufacturing Associate, your duties are to carry out a range of manufacturing activities to contribute to the achievement of GMP standards of quality, cost and service within the manufacturing operation.

Major Role & Responsibilities

• Complete manufacturing work‑steps under general supervision and within the defined standards according to specifications using only the defined production aids, equipment, tooling and materials.
• Verify at each work‑step, by utilizing appropriate tests and inspections, that the quality of all product or components produced meets clearly defined quality standards.
• Perform simple internal set‑up on manufacturing equipment to required standard.
• Verify in conjunction with the Quality department the quality of product produced prior to recommencement of production.
• Ensure the required levels of raw materials are maintained by controlling the appropriate Kanbans within the department.
• Complete on line documentation and highlight deviations to appropriate persons.
• Participate in identifying, drawing attention to and resolving problems on the line as member of the department teams.
• Ensure that all the required documentation and charts are completed correctly as per approved S.O.P.’s.
• Follow all G.M.P. procedures such as good housekeeping, hygiene and safety practices etc. as outlined by the various regulatory bodies such as FDA, ISO and KCI Corporate Policies.
• Ensure that the Time Keeping and Attendance policy is observed and followed.
• Abide by Environmental, Health and Safety (EHS) Policies and any relevant other EHS documentation.
• Comply with all relevant training required and adhere to relevant associated documentation.
• Follow strict adherence to the requirements of CGMP.
• Actively contribute to the enhancement of compliance initiatives for areas of responsibility.

Skills and Expertise

• Education: 2nd Level education or 2 years equivalent experience in a similar work environment.
• Experience: Two (2) years experience in medical device or similar industry with an established track record.
• Good verbal and written communication skills.
• Strong teamwork abilities.
• Commitment to achievement of manufacturing excellence.
• High level of flexibility: shift changes/travel commitments/training courses/preventative maintenance and project support.

Work Information

Work location: Athlone, Ireland
Work type: Onsite
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

Solventum is an equal opportunity employer and values diversity. We do not discriminate on the basis of race, religion, gender, sexual orientation, age, civil status, disability, family status, or membership of the travelling community.