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For nearly 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 Summary
Full-time Scientific Research In-Vitro Associate 1 (Microbiologist) required to operate under the Technical Services Department for our Microbial Solution Site in Dublin.
The successful candidate will be responsible for processing microbial and LAL testing samples in our CELSIS laboratory utilising various technology platforms.
Essential Duties And Responsibilities
* Perform LAL testing for different studies as assigned encompassing a full range of LAL techniques, gel-clot, kinetic and PTS.
* Perform IQ, OQ, PQ of lab equipment such as Biotek, PTS and maintain appropriate documents.
* Perform contract testing laboratories for Celsis and LAL including method development studies, method validation studies, accessory release, CSE/RSE, LAL water etc as required.
* Perform laboratory activities necessary to isolate, grow and maintain cultures of bacteria.
* Perform and manage bioburden testing, membrane filtration and, cleaning validations.
* Ensure adherence to pertinent regulatory requirements (cGMP, FDA, ISO) and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
* Collaborate with inventory check of laboratory consumables and assist with general housekeeping of the laboratory, performing equipment maintenance and scheduling instrument calibrations.
* Assist management with development and revision of departmental standard operating procedures and qualification documents.
* Perform all other related duties as assigned.
Job Qualifications
* Education: Degree in Microbiology, Biology or a related discipline.
* Experience: Established and demonstrable track record of related experience in a microbiology laboratory setting. Experience in cGMP pharmaceutical microbiology environment is preferred.
* Other: Knowledge of windows based programs such as word and excel and a minimum knowledge of algebra.
Physical Demands
* Requires colour vision, close vision and the ability to adjust focus.
* Regularly works in a stationary position; occasionally moves about the lab/office to access supplies and equipment.
* Regularly communicates with other employees/customers and must be able to exchange accurate information verbally and in written form.
* Occasionally operates a computer.
* Occasionally must perform manual handling.
* Must be able to wear personal protective equipment (PPE) according to company standards.
Work Environment
* Working in a lab environment. May work with sharp objects, near toxic or caustic chemicals, with biohazards, may be exposed to fumes or airborne particles, unpleasant odors and may be exposed to the risk of radiation.
* The noise level in the work environment is usually quiet to moderate.
* While performing the duties of this job, the employee regularly wears protective clothing and equipment (lab coat and safety glasses) when exposed to the laboratory area
About Microbial Solutions
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.
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 to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and 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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past 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.
229090
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