Analytical Supervisor

Charles River Laboratories; Ballina; On-site; EUR 70,000 - 90,000; Full time

Job summary

Charles River Laboratories in Ballina, Co. Mayo, Ireland, seeks an Experienced Analytical Supervisor for its Biologics Division. You will oversee the Analytical team to ensure SOP and GMP adherence, coordinate training, and maintain data integrity across projects.

The role involves audits, regulatory liaison, method transfers, data review and collaboration with clients to deliver high-quality biologics testing services. A BSc in a relevant science and 3+ years GMP experience are required.

Qualifications

• Minimum 3 years in scientific research with GMP exposure.
• Experience supervising staff in a regulated lab.
• Proficiency with analytical techniques used in biotech/pharma.

Responsibilities

• Oversee analytical team work quality per SOPs and GMP.
• Develop training for staff on assays and equipment.
• Participate in client and regulatory audits and prepare SOPs.
• Maintain data integrity and archive records per SOPs.

Skills

Analytical supervision

GMP compliance

Leadership/People management

HPLC

Regulatory audits

Education

BSc in Chemistry/Biochemistry/Biotechnology

Tools

LIMS

Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well‑being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Description

We are seeking an experienced Analytical Supervisor for our Biologics Division located in Ballina, Co. Mayo, Ireland.

Responsibilities

• Oversee the quality of work produced by the Analytical team and ensure it is conducted in accordance with Standard Operating Procedures and the principles of GMP.
• Implement and supervise safe working methods within the team and inform and instruct staff of these. Comply with all 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 working on client‑specific projects.
• Prepare costings and proposals based on protocols/project plans of proposed work by clients.
• Assist in the transfer of assays from clients to the Analytical Services Department where appropriate.
• Participate in regulatory and client audits and liaise with clients as required.
• Generate appropriate SOPs.
• Assist Project Leaders with research technical information for incoming new enquiries.
• Compile audit responses in conjunction with the team and the Analytical Technical Operations Manager.
• Support staff with deviations and laboratory investigation reports.
• Review raw data.
• Ensure all raw data and test results—including protocols, reports, etc.—are retained and archived according to Charles River Laboratories SOPs.
• Prepare presentations and deliver them 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.
• Liaise with other departments to ensure that laboratory areas and all equipment are maintained in appropriate working conditions.
• Purchase new equipment and spare/replacement parts as required.
• Maintain stock of supplies (chemicals, consumables) needed for routine activities within the team.
• Schedule daily tasks for analysts, ensuring appropriate workload is not exceeded.

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/managing staff.
• Experience with analytical techniques (e.g., HPLC, compendials, CE‑SDS, icIEF, GC) essential.
• Ability to problem‑solve and work on own initiative.
• Excellent communication and organizational skills.

About Biologics Testing Solutions

With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. We offer a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, supporting clients throughout the biologic development cycle—from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand‑alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent and over 200 licensed products are supported by our biologics testing solutions team.

About Charles River

Charles River is an early‑stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non‑GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness and increases speed to market. With over 20,000 employees within 110 facilities in over 20 countries worldwide, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients’ unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies, hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well‑being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.