Overview
Join to apply for the Analytical Supervisor role at Charles River Laboratories.
For 75 years, Charles River employees have helped in discovery, development and safe manufacture of new drug therapies. Our team supports health and well-being worldwide, and we value diverse backgrounds. This role is based in Ballina, Co. Mayo, Ireland.
The Analytical Supervisor reports to the Analytical Laboratory Manager and will oversee analytical testing within the Analytical Department. A team of 8-10 Analysts will report to this role.
Responsibilities
* Oversee the quality of work produced by the Analytical team and ensure it is conducted in accordance with Standard Operating Procedures and GMP principles.
* Implement and supervise safe working methods; ensure compliance with Health and Safety regulations and procedures.
* Develop, coordinate and implement training for staff on technical aspects of new and existing assays.
* Provide feedback on performance to analysts on client-specific projects.
* Assist in preparing costings and proposals based on client protocols and project plans.
* Assist in transfer of assays from clients to Analytical Services Department where appropriate.
* Participate in regulatory and client audits and liaise with clients as required.
* Assist in generating appropriate SOPs.
* Assist Project Leaders with research technical information for new enquiries.
* Compile audit responses in conjunction with the team and the Analytical Technical Operations Manager.
* Support staff with deviations and laboratory investigation reports.
* Raw data review and retention of all raw data, test results, protocols and reports according to SOPs.
* Prepare and deliver presentations to the Analytical Services Department team and to Clients as required.
* Assist in Test Item Receipt (LIMS), storage, disposal and decontamination.
* Liaise with consultants and external services (e.g., subcontract laboratories) as appropriate.
* Coordinate with other departments to maintain equipment and laboratory areas in appropriate condition.
* Purchase new equipment and spare parts as required.
* Maintain stock of chemicals and consumables necessary for routine activities within the team.
* Schedule daily tasks for analysts to ensure appropriate workload management.
Qualifications
* BSc in a relevant science discipline (e.g., Chemistry, Biochemistry or Biotechnology)
* A minimum of 3 years relevant experience in scientific research, preferably within a GMP-regulated environment (EMEA/FDA) in the pharmaceutical, medical device, or CRO industry
* Proven track record of supervising or managing staff
* Experience in analytical techniques (e.g., HPLC, compendials, CE-SDS, icIEF, GC) is essential
* Ability to problem solve and work on own initiative
* Excellent communication and organizational skills
Profile and Requirements
About Biologics Testing Solutions: With more than 50 years of experience, the Biologics group provides regulatory expertise and testing services across biotechnology and pharmaceutical projects, including contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs.
About Charles River: Charles River is an early-stage contract research organization (CRO) offering GLP and non-GLP discovery and safety assessment services, with a broad portfolio to support clients from target identification through preclinical development. We operate globally with more than 20,000 employees in 110 facilities across 20 countries, serving global pharmaceutical, biotechnology, government, hospital and academic clients.
We are committed to fostering belonging and diversity in the workplace.
Job Details
* Seniority level: Mid-Senior level
* Employment type: Full-time
* Job function: Production
* Industries: Automation Machinery Manufacturing
Location: Ballina, County Mayo, Ireland
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