Associate Biopharma Supervisor

Employer
Thornshaw Recruitment
Location
Westmeath, Leinster (IE)
Salary
Negotiable depending on experience
Start date
8 Jan 2023
Closing date
7 Feb 2023

View more

Discipline
Quality, GMP, QC Analyst
Hours
Full Time
Contract Type
Permanent
Experience Level
Management
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Job Details

My client an expanding global CRO company, is currently recruiting for Associate Group Leaders/ QC Supervisors to join their Biopharmaceutical team.

Permanent positions, excellent benefits such as health insurance, pension and joining bonus.

 

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.

 

Job Qualification

 

Education & 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, EMA and FDA guidance's. Knowledge and experience of a wide range of techniques, HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA, spectrophotometry.

If you are interested in applying for this role please call Zoe on +353 1 2784671 or email zhamilton@thornshaw.com

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com

Company

Thornshaw Scientific Recruitment has been providing a reputable recruitment service to the Biopharmaceutical, Pharmaceutical, Clinical Research, Medical Device, Food and Healthcare industries for over 15 years.

Our strategic focus has always been to grow the business in a way which has ensured the quality of our service has never been compromised. In 2005 Thornshaw was acquired by Cpl Resources, one of Europe’s most successful recruitment companies.

Find Us
Website
Telephone
00 353 (1) 278 4671
Location
Barton House
6 Old Dublin Road
Stillorgan
Co. Dublin
IE

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