Process Assurance Operator

freudenberg; Carrick-on-Shannon; On-site; EUR 28,000 - 42,000; Full time

Job summary

Freudenberg Medical Ireland Ltd. in Ireland is seeking candidates to join the manufacturing team and uphold strict safety, quality, and performance standards. The role focuses on complying with OHS, GMP, and customer requirements while contributing to continuous improvement initiatives.

Applicants should be team-oriented with a solid educational background and strong communication skills. This position is based in Carrick-on-Shannon, County Leitrim, and will require on-site work at the facility.

Qualifications

• Candidates should have a good standard of education and be willing to work within a team environment.
• Interview selection based on experience, aptitude & references.
• Strong interpersonal and communications skills.

Responsibilities

• Adhere to Plant Safety and Health & Safety requirements to protect yourself and others.
• Be aware of environmental impacts and implications of non-conformance.
• Ensure Cleanroom, housekeeping & GMP requirements are followed.
• Ensure product is manufactured per procedures meeting internal quality and productivity goals.
• Ensure process control requirements including first piece inspection and in-process inspections with timely adjustments.
• Carry out effective product change-overs and embed waste reduction in processes.
• Highlight and prevent product and process non-conformances as per procedures.
• Participate in Customer Complaint investigation and resolution.
• Participate in plant Corrective Action and Continuous Process Improvement programmes.
• Participate in the Internal Training Programme.

Skills

Interpersonal skills and communication

Education

Good standard of education

Job description

Working at Freudenberg: We will wow your world!

Responsibilities:

• Adhere to Plant Safety requirements and Health & Safety requirements relating to your work, assuming responsibility for those aspects of the OH&S System over which you have control to ensure the health and safety of yourself and others.
• Be aware of the potential environmental impacts associated with your work and the implications of non-conformance.
• Ensuring that all C leanroom, housekeeping & GMP Requirements / procedures are adhered to.
• Ensuring that product is manufactured in accordance with Customer / VISTAMED procedures & blueprints while meeting pre-determined internal quality & productivity goals.
• Ensuring that all process control requirements are adhered to including first piece inspection , in-process inspections and that timely adjustments are carried out , in accordance with production procedures.
• Ensuring that product change‑overs are carried out effectively and waste reduction methods are integrated into all processes.
• Take action where necessary to highlight and prevent product and process non‑conformance's in accordance with our non-conforming procedure.
• Participation in Customer Complaint investigation & resolution.
• Participation in plant Corrective Action & Continuous Process Improvement programmes.
• Participation in the Internal Training Programme.

Qualifications:

• Candidates should have a good standard of education and willing to work within a team environment, to strict regulations and deadlines.
• Interview selection based on experience, aptitude & references.
• Strong interpersonal and communications skills.

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Freudenberg Medical Ireland Ltd.