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Manufacturing Team Members

Munster   •  Negotiable  •  Contract/Temporary, Full time


Manufacturing Team Members

Waterford, Ireland

12 month contract

13.80 per hour

A Global Pharmaceutical company in Waterford Ireland is looking for Manufacturing Team Members to support with the final packaging of products before release whilst ensuring Quality and Safety regulations are adhered too. There is also positions within the same team as an Inspection Manufacturing Team Member, this role is focussing more on inspecting the final products ready for packaging.

These positions are a great opportunity for someone who may want to begin their career within the Pharmaceutical industry or someone who has previous experience looking to develop their career.

Shift work may be required so applicants must be flexible towards their working days/ hours.

Key responsibilities;

  • Maintain and support scheduled adherence to production and OEE
  • Complete as relevant SOPs and training
  • Conduct duties in a safe manner and report all safety issues or concerns
  • Maintain the required standard of housekeeping and hygiene
  • Ensure all documentation is completed accurately and RFT (right first time)
  • Ensure complete handover takes place as appropriate
  • Attend all site and team meetings as required
  • Actively contribute to continuous improvement initiatives
  • Support cross-training plan when required
  • Participate in Data Collection and Analysis
  • Participate in investigations as required
  • Operate equipment as part of the production line(s) to achieve the required level of production output
  • Support team in achieving goals/targets.
  • Adherence to aseptic practices and procedures
  • Support Internal & External Audits
  • Deviation and Capa tasks/LCR/CSRR/GMP Permits
  • Ensure compliance to cGMP at all times

Experience/ Qualifications;

  • Competent in the operation, cleaning, maintenance of all manufacturing equipment
  • Engineering qualification desirable
  • Demonstrated understanding of mechanical operations
  • Knowledge of cGMP
  • Understands site KPIs
  • Able to understand process scheduling requirements within a manufacturing environment
  • CAPA, deviation knowledge

For more information please contactMark.bathe@cpl.com

  • Agency: Cpl Life Sciences
  • Reference: JO-2206-494677
  • Posted: 13th June 2022
  • Expires: 11th July 2022

Cpl Life Sciences

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