Production Operator - 3 Shift Rotating Cycle

Uniting Holding

Loughrea

On-site

Full time

14 days+
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Job summary

A leading pharmaceutical company in Loughrea is seeking a Production Operator to join their dynamic team. You will be responsible for manufacturing and packing products in compliance with regulatory standards, completing necessary documentation, and ensuring equipment is functioning correctly. Ideal candidates will have at least 1 year of experience in a GMP environment and possess strong communication and problem-solving skills. This role offers a rotating shift pattern and promotes a diverse workplace culture.

Qualifications

  • At least 1 years’ experience in a Pharmaceutical FDA/HPRA or manufacturing environment preferable.
  • Excellent knowledge of GMP & GDP requirements desirable.

Responsibilities

  • Manufacturing/packing product to cGMP/regulatory standards.
  • Accurate completion of all necessary documentation.
  • Carry out IPC checks as outlined in company documentation.
  • Ensure machines/equipment are maintained and working correctly.
  • Carry out minor machine/equipment adjustments as appropriate.

Skills

Collaboration
Problem-solving
Communication
Organisation

Education

Experience in Pharmaceutical or manufacturing environment

Job description

Production Operator - 3 Shift Rotating Cycle

This is an opportunity to be part of a dynamic team within the Production and Manufacturing function. We are looking for individuals who will support and drive Chanelle Pharma’s vision to be the most valued global provider of high quality, competitively priced pharmaceutical products and to provide excellent services and support to our customers.

In this role you will report into Production Supervisor / Production Manager.

Location: Onsite in our Loughrea production facility.

As our Production Operator, you will be responsible for:

  • Manufacturing/packing product to cGMP/regulatory standards as outlined in company documentation.
  • Accurate completion of all necessary documentation.
  • Carry out IPC checks as outlined in company documentation.
  • Ensure machines/equipment are maintained and working correctly.
  • Carry out minor machine/equipment adjustments as appropriate.
  • Clean machines/work area in accordance with standard operating procedures.
  • Assist with training as required.
  • Attainment of targets relevant to work centre.
  • Adherence to health and safety procedures.
  • Ensure compliance to documented procedures and cGMP requirements as outlined in company procedures.
  • Maintenance of hygiene/housekeeping standards in all production areas.
  • Comply to terms and conditions as outlined in your contract of employment.

Education & Experience:

  • At least 1 years’ experience in a Pharmaceutical FDA/HPRA or manufacturing environment preferable.
  • Excellent knowledge of GMP & GDP requirements desirable.

Skills & Competencies:

  • Ability to build relationships and collaborate with others is vital.
  • Demonstrate and practice company values on a daily basis.
  • Self-starter with demonstrated efficient work methods, analytical & problem-solving skills and ability to handle multiple tasks.
  • Good communication, leadership and people management skills are essential.
  • Strong organisational and problem-solving ability.

Role Hours (shifts rotate every 3 weeks):

  • Day shift: 08.00 – 16.10 Mon – Thurs, 08.00 – 15.10 Fri.
  • Evening shift: 16.00 – 12.10 Mon – Thurs, 15.00 – 22.10 Fri.
  • Night shift: 12.00 – 08.10 Mon – Thurs, 22.00 – 05.10 Fri.

Applicants from diverse backgrounds, including those returning after a career break or with transferable skills from non-traditional career paths, are encouraged to apply. We value varied experiences and are committed to fostering an inclusive environment that supports individuals with disabilities.

We are an equal opportunities employer and welcome applications from all qualified candidates.

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