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Occupli

Production Operator

Cork city, IEPresencialContratoTempo integral

Publicado 9 de set. de 2026

Esta vaga foi publicada em EN

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 escalate 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.


Benefits


  • 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.

Apply Now

If you are an experienced Production Operator looking for your next opportunity within the pharmaceutical manufacturing sector, Occupli would be delighted to hear from you.

Apply today or contact the Occupli recruitment team for further information.



Resumo da função

Tipo de vaga

Tempo integral

Competências necessárias

Good Manufacturing Practice (GMP) compliance and SOP adherenceBatch record documentation and accurate data entryProcess monitoring and in-process control checksQuality control checks and deviation identification/escalationSampling procedures and sample handlingSanitation, equipment cleaning and production area housekeepingMaterials identification, handling and storageHealth, safety and PPE complianceRoot cause investigation and support for corrective actions/continuous improvementCross-functional collaboration with Production, Quality and EngineeringUse of manufacturing/business IT systems (e.g., SAP)Attention to detail and accuracy in documentationVerbal and written communication (fluent English)

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