Production Operator

PE Global (UK); Carlow; On-site; EUR 28,000 - 36,000; Full time

Job summary

A biotechnology firm in Carlow is seeking a Production Operator for an 11-month initial contract working a 4 cycle-shift pattern. The role involves supporting continuous improvement, performing root cause analysis, and ensuring compliance with safety and GMP standards. Candidates should have a Leaving Certificate and ideally prior experience in manufacturing. Interested individuals should submit an updated CV or apply through the provided link.

Qualifications

• Understanding of Good Manufacturing Practices (cGMP).
• Experience in a manufacturing environment, preferably GMP setting.
• Ability to comply with safety procedures and regulations.

Responsibilities

• Support continuous improvement and perform root cause analysis.
• Highlight roadblocks related to safety, quality, and delivery.
• Engage in Tier 1 process and adhere to safety procedures.
• Engage in Tier 1 process at start and end of shift; ask relevant questions and provide details.
• Comply with Site Policies, Procedures, regulatory requirements and cGMP practices.

Skills

Root cause analysis

Problem solving

Safety compliance

Education

Leaving Certificate or equivalent

Apprenticeship, Certificate or Diploma in related discipline

Job description

PE Global is currently recruiting for a Production Operator on behalf of our Biotech client based in Carlow:

11-month initial contract – Working a 4 cycle-shift pattern

Role Functions

• Support continuous improvement by active participation in investigations and investigation reports, execution/development of change control, and contribution to Kaizen events and projects as appropriate. Perform root cause analysis, using standard tools and methods, to resolve system issues e.g. FMEA, Fishbone diagrams, 5 why’s etc.; implement subsequent corrective action through the change management system.
• Highlights roadblocks or issues from a people, safety, quality or delivery perspective in a timely manner.
• Able to perform routine day to day problem solving for assigned area independently or when working as part of a team
• Engage in Tier 1 process at both start and end of shift. Asking relevant questions and providing detailed information
• Required to comply with Site Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
• Take ownership of your own safety & adhere to all safety procedures and programs.
• Obtain and Maintain all required safety certifications independently.
• Work collaboratively to drive a safe and compliant culture in Carlow.

Qualifications & Education

• Leaving Certificate or equivalent required
• Apprenticeship, Certificate or Diploma preferred, ideally in a related discipline
• Would typically have prior related work experience; ideally in a manufacturing, preferably GMP setting.

Interested candidates should submit an updated CV.

Please click the link below to apply, or alternatively send an up to date CV to [e-mail]

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***