External - Manufacturing Associate (m/f/x)

IRL KCI Manufacturing Unlimited Company; Athlone; On-site; EUR 28,000 - 36,000; Full time

Job summary

Solventum is a healthcare company focused on improving lives by solving big challenges for healthcare professionals. A manufacturing role within GMP-aligned operations is available, requiring a background in medical devices and strong team collaboration.

Responsibilities include completing manufacturing steps, ensuring quality at each stage, managing Kanbans, documenting activities, and maintaining compliance with CGMP, EHS, and regulatory standards.

Qualifications

• 2nd level education or 2 years of equivalent experience in a similar work environment.
• Two years of experience in the medical device or a similar industry with an established track record.
• Good verbal and written communication skills; strong teamwork abilities; commitment to manufacturing excellence.

Responsibilities

• Carry out a range of manufacturing activities to contribute to GMP standards of quality, cost, and service within the manufacturing operation.
• Complete manufacturing work-steps under general supervision according to specifications using defined production aids, equipment, tooling, and materials.
• Verify at each work-step, using appropriate tests and inspections, that the product or components produced meet defined quality standards.
• Perform simple internal setup on manufacturing equipment to the 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 a member of department teams.
• Ensure all required documentation and charts are completed correctly as per approved SOPs.
• Follow GMP procedures such as good housekeeping, hygiene, and safety practices as outlined by regulatory bodies (FDA, ISO) and corporate policies.
• Ensure Time Keeping and Attendance policy is observed and followed.
• Adhere to Environmental, Health and Safety (EHS) Policies and relevant EHS documentation.
• Comply with relevant training and associated documentation.
• Follow CGMP requirements and contribute to compliance initiatives for areas of responsibility.

Skills

Good verbal and written communication

Teamwork

Education

Secondary education or equivalent experience

2 years experience in medical device or similar industry

Job description

Overview

Solventum is a healthcare company focused on improving lives by solving big challenges for healthcare professionals. This description outlines the responsibilities and requirements for a manufacturing role within the company, aligned with GMP standards and regulatory guidance.

Responsibilities

• Carry out a range of manufacturing activities to contribute to GMP standards of quality, cost, and service within the manufacturing operation.
• Complete manufacturing work-steps under general supervision according to specifications using defined production aids, equipment, tooling, and materials.
• Verify at each work-step, using appropriate tests and inspections, that the product or components produced meet defined quality standards.
• Perform simple internal set-up on manufacturing equipment to the 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 a member of department teams.
• Ensure all required documentation and charts are completed correctly as per approved SOPs.
• Follow GMP procedures such as good housekeeping, hygiene, and safety practices as outlined by regulatory bodies (FDA, ISO) and corporate policies.
• Ensure Time Keeping and Attendance policy is observed and followed.
• Adhere to Environmental, Health and Safety (EHS) Policies and relevant EHS documentation.
• Comply with relevant training and associated documentation.
• Follow CGMP requirements and contribute to compliance initiatives for areas of responsibility.

Qualifications & Requirements

• Education: 2nd level education or 2 years of equivalent experience in a similar work environment.
• Experience: Two (2) years in the medical device or a similar industry with an established track record.
• Skills: Good verbal and written communication skills; strong teamwork abilities; commitment to manufacturing excellence.
• Other: High level of flexibility including shift changes, travel commitments, training courses, preventative maintenance, and project support.
• Legal authorization: Must be legally authorized to work in the country of employment without sponsorship for employment visa status.

Well-being & Diversity

Solventum offers programs to support well-being and aims to provide competitive pay and benefits. We are an equal opportunity employer and value diversity. We do not discriminate on the basis of race, religion, gender, sexual orientation, age, civil status, disability, family status, or membership of a traveling community.

Privacy & Terms

Please review our privacy statement and terms of use linked in the job materials. Acceptance of terms may be required during application submission.

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