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Pharma/Biopharma Team leader

  • Salary: Negotiable
  • Job type: Permanent
  • Location: Westmeath
  • Sector: Science
  • Date posted: 19/09/2017
  • Job reference: J353525A
This vacancy has now expired.

QC Team Leader (Pharma & Biopharma)


Biopharmaceutical Team Leader

Due to our clients continued success and growth, we are currently looking to recruit an Associate Group Leader to be based in their Biopharm department of their GMP Lab in Athlone, Ireland.

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.
  • 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, microbiology, 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.

Qualification

  • Educated to a Bachelor's Degree level in a relevant area
  • 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 with a wide range of chromatography techniques: HPLC, UPLC, GC
  • Experienced in method development and validation

The successful candidate can look forward to job stability with a leading Company that has experienced year-on-year growth. With future expansion plans, there is the opportunity to progress in your career. There is a generous salary, medical insurance, pension, life insurance and relocation assistance to those qualified candidates based outside of the Republic of Ireland.

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