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Analytical Group Supervisor

Reference:KSAGRY-382050 Location: Offaly
Qualification:DegreeExperience:4-5 Years
Job Type:PermanentSalary: €50000 - €55000

Analytical Group Supervisor

This company provides laboratory services that are designed to provide the best and highest level of service to our clients. They offer job stability and the business has experienced year-on-year growth. With future expansion plans, there is the opportunity to progress in your career.

The role of Analytical Group Supervisor is to provide support to the BioPharm department by providing management and direction to a group of laboratory staff and resources for project activities and needs, overseeing daily operations to monitor quality and project timeliness, and assist in preparation and implementation of company policies, quality systems and training programs. You will have ownership to ensure responsiveness to the client and overall client satisfaction. This position is lab based, with direct supervisory responsibilities of a small group of Scientists.

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.
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.

This role offers an excellent opportunity for someone who has previous GMP experience in a small molecule environment coupled with proven record of team leadership; who would now like to embrace a new technical environment/Biopharm specific techniques.
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. Our client offers a generous salary, medical insurance, pension, life insurance and relocation assistance to those qualified candidates based outside of the Republic of Ireland.

If you would like further Information you can contact the recruiter directly:

Kevin Silke | Tel: +353 (0) 1 507 9255