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Analytical Lab Supervisor

Expired
  • Salary: Negotiable
  • Job type: Permanent
  • Location: Westmeath
  • Sector: Science
  • Date posted: 21/08/2018
  • Job reference: BBBH13328

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Analytical Lab Supervisor


My client, a leading multinational pharmaceutical organisation is currently seeking am Analytical Lab Supervisor to join their expanding BioPharmaceutical team.


In this position you will be tasked providing management within the lab and ensuring project activities and timeline are met. You will have the opportunity to work both with direct reports, managing a team of analysts, and external stakeholders. Designing experimental study and participates in technical troubleshooting, you will have the opportunity to assist both senior group leaders and managers.

Key responsibilities:

  • Allocation, scheduling and managing laboratory resources for group's project activities and updates LIMS for project status. Reviews timesheet reports for billing accuracy.
  • Preparation, review and approval of study protocols, project status reports, final study reports and other project-related technical documents.
  • Reviewing data for technical quality and compliance to protocols, methods and SOPs. Review and approve laboratory investigations, deviations, QA facility and data audits. Assists in client and regulatory authority audits.
  • Responding to client questions and needs; leads client technical meetings.
  • Assisting in preparation of proposals, project definition and pricing.
  • Coordinating and prioritizing project activities with internal functional groups (physical testing, analytical development, etc.) and support functions (QA, sample management, etc.)
  • Preparation and implementing SOPs and company operational policies. Ensuring adherence and making recommendations to quality system improvements.



Skills and experience:

  • Educated to a Bachelor's Degree level in a relevant area, ie chemistry, biochemistry
  • Management experience in the pharmaceutical, biotech or analytical contract laboratory industries
  • Stability/QC/analytical R&D/project and program management.
  • Direct supervision of technical staff.
  • Full understanding of GMP requirements, client SOPs, ICH guidelines, EP and USP requirements and EMEA and FDA guidance's.
  • Knowledge and experience of a wide range of techniques, HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA, spectrophotometry.



For more information on this and other potential opportunities please contact Kathryn Whyte on 016455250.