CPL

CPL

ANALYTICAL GROUP SUPERVISOR - BIOPHARM D


Posted on:
29/06/2020
Location:
WESTMEATH
Salary:
NEGOTIABLE
Job type:
PERMANENT
Job reference number:
15503530
Client ID:
JO-1808-414775_277
My client, a global CRO is actively seeking candidates for the permanent role of Analytical Group Supervisor / Associate Group Leader, Biopharm .

Key responsibilities:

  • Management of a team of analysts
  • 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.
  • Designing experimental study and participates in technical troubleshooting.
  • 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.)
  • Assisting senior group leaders and/or managers in their responsibilities.
  • Preparation and implementing SOPs and company operational policies. Ensuring adherence and making recommendations to quality system improvements.

Desired Qualifications 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 full details please contact Zoe at +353 1 2784671 or email your CV in confidence to zhamilton @thornshaw.com
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