Manufacturing Associate (m/f/x)

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.