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
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 was first established in 1999 and since then has become a leader in Scientific recruitment. In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.
Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.
Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.
Our Industries
We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years.
Our Specialities
Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.
Our Mission
For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com
- Website
- http://www.thornshaw.com/
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