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Production Supervisor GMP Clean-Room Facilities

Job description

Looking for an experienced Production Supervisor (permanent job) to take up a lead in managing a team of staff in GMP Pharmaceutical/Biotech client.

Contact

If you are interested in this role apply below. I also have more senior roles within QC, QA, QP, Validation, CQV, and other areas of pharmaceutical, medical device and biologics companies. Send me an email to schedule a confidential chat (014744692) - to andrius at sigmar.ie

The Job

  • Supporting production operations on a daily basis to meet commitments to customers.
  • Providing direction to Shift leads carrying out their daily tasks,
  • Monitoring compounding unit activities to ensure compliance with internal policies/ procedures and cGMP.
  • In conjunction with the Production Manager, Planning and organisation of resources in line with the operational plan for the compounding unit.
  • Facilitating best use of unit resources to the various unit functions (e.g. preparation, compounding, checking, labelling, training, QMS etc.)
  • Support staff training and development while ensuring that training is completed in a timely manner and that training records are properly maintained.
  • Supports all people management activities – , performance management, development, training in accordance with Baxter’s leadership standards.
  • Organization of holidays and overtime
  • Support Non-Conformances and CAPAs assigned under production responsibility. Support investigation and the identification and implementation of corrective action.
  • Assist in the introduction of New Products and Process Change Controls
  • Support Preparation of Production KPI’s – Stock control, Schedule compliance and Financial Reports.
  • Organisation and co-ordination of the environmental monitoring activities in conjunction with micro-laboratory
  • Organisation and co-ordination of calibration and maintenance activities in conjunction with Technical Services.
  • Stock checks of manufactured product to ensure that product is accurately reconciled with production and dispatch records and to identify and discard expired stock
  • Ensuring that housekeeping is carried out in accordance with cleaning procedures and schedules
  • Review and update of production procedures and in the introduction of new procedures as appropriate.
  • Support procurement and inventory management team to ensure regular stock checks of raw materials and goods are performed and that adequate stock levels are maintained to meet production requirements
  • Support Integration activities and projects/ tasks as assigned
  • As required, undertake other duties commensurate with the level of responsibility outlined above.
  • Compliance to Good Manufacturing Practices (GMP) or Good Distribution Practices (GDP), as applicable
  • Compliance to Environmental Health & Safety (EHS) requirements

What are the Requirements

  • Diploma in a science/healthcare/Technology is preferred
  • 5 years GMP experience
  • 3 years’ experience in a team lead / supervisor role
  • GMP manufacturing environment experience is necessary
  • Knowledge of GMPs in a sterile manufacturing environment

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