ZR_947_JOB

Zohorecruit

Cork

On-site

EUR 28,000 - 36,000

Full time

14 days+
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Job summary

Occupli is partnering with a leading pharmaceutical manufacturing site in Cork to recruit a Production Operator. The role focuses on adhering to GMP, maintaining documentation accuracy and supporting daily production activities within a highly regulated environment.

You will work alongside Quality, Engineering and other functions to ensure compliant, safe and efficient operations and contribute to a Right First Time culture through precise execution of manufacturing tasks.

Qualifications

  • Previous experience within a pharmaceutical, life sciences, GMP or other highly regulated manufacturing environment.
  • Good understanding of GMP principles, SOPs and controlled documentation.
  • Experience working with production records, batch documentation or similar quality-controlled systems.
  • Strong attention to detail with a high level of accuracy in documentation and data entry.
  • Ability to identify and escalate quality, safety or process issues appropriately.
  • Comfortable working as part of a production team in a regulated environment.
  • Good computer skills; SAP experience would be advantageous.
  • Strong commitment to health, safety, quality and environmental standards.
  • Good communication skills and fluent English.

Responsibilities

  • Support day-to-day production activities in line with approved procedures and manufacturing requirements.
  • Monitor production processes and carry out routine in-process checks and controls.
  • Complete production records, batch documentation and associated records accurately and in real time.
  • Carry out routine quality and process checks as required.
  • Support sampling activities and liaise with Quality teams where required.
  • Identify and promptly report any process abnormalities, deviations or quality concerns.
  • Maintain high standards of GMP, hygiene and housekeeping across production areas.
  • Clean production equipment and work areas in accordance with established procedures.
  • Ensure materials are correctly identified, handled and stored.
  • Follow all site safety procedures, risk assessments and environmental requirements.
  • Use appropriate PPE and safety equipment at all times.
  • Contribute to investigations, corrective actions and continuous improvement initiatives where required.
  • Work collaboratively with Production, Quality, Engineering and other site functions to maintain safe and efficient operations.
  • Support a strong Right First Time culture through accurate execution and documentation of manufacturing activities.

Skills

GMP experience
Attention to detail
Teamwork
Fluent English

Education

Relevant qualification in pharmaceutical manufacturing or related discipline

Job description

Cork city, Ireland | Posted on 09/09/2026

Production Operator – Pharmaceutical Manufacturing

Occupli is delighted to partner exclusively with a leading pharmaceutical manufacturing organisation to recruit a Production Operator for their Cork operation.

This is an excellent opportunity for an experienced Production Operator to join a highly regulated manufacturing environment where quality, safety, compliance and attention to detail are central to the role.

The successful candidate will work as part of an established production team, supporting day-to-day manufacturing activities while ensuring all processes and documentation are completed accurately and in accordance with site procedures.

Key Responsibilities
  • Support day-to-day production activities in line with approved procedures and manufacturing requirements.
  • Monitor production processes and carry out routine in-process checks and controls.
  • Complete production records, batch documentation and associated records accurately and in real time.
  • Carry out routine quality and process checks as required.
  • Support sampling activities and liaise with Quality teams where required.
  • Identify and promptly report any process abnormalities, deviations or quality concerns.
  • Maintain high standards of GMP, hygiene and housekeeping across production areas.
  • Clean production equipment and work areas in accordance with established procedures.
  • Ensure materials are correctly identified, handled and stored.
  • Follow all site safety procedures, risk assessments and environmental requirements.
  • Use appropriate PPE and safety equipment at all times.
  • Contribute to investigations, corrective actions and continuous improvement initiatives where required.
  • Work collaboratively with Production, Quality, Engineering and other site functions to maintain safe and efficient operations.
  • Support a strong Right First Time culture through accurate execution and documentation of manufacturing activities.
Requirements
  • Previous experience within a pharmaceutical, life sciences, GMP or other highly regulated manufacturing environment.
  • Good understanding of GMP principles, SOPs and controlled documentation.
  • Experience working with production records, batch documentation or similar quality-controlled systems.
  • Strong attention to detail with a high level of accuracy in documentation and data entry.
  • Ability to identify and escalase quality, safety or process issues appropriately.
  • Comfortable working as part of a production team in a regulated environment.
  • Good computer skills and experience using manufacturing or business systems; SAP experience would be advantageous.
  • Strong commitment to health, safety, quality and environmental standards.
  • Good communication skills and fluent English.
Education & Experience
  • A relevant qualification in pharmaceutical manufacturing, science, engineering or a related discipline would be advantageous.
  • Relevant experience within a pharmaceutical or GMP-regulated manufacturing environment will also be considered.
  • Opportunity to join an established pharmaceutical manufacturing operation.
  • Structured and highly regulated working environment.
  • Exposure to GMP manufacturing, quality and continuous improvement activities.
  • Supportive team environment.
  • Opportunity to develop your experience within the pharmaceutical/life sciences sector.
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