Technician I Molecular Biology
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.
About the role
Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services.
Responsibilities
- Perform laboratory activities necessary for molecular biology testing including but not limited to:
- Reagent preparation including buffers, chemical solutions, complex mixtures, and media preparations according to standard test methods.
- Perform tasks using aseptic techniques including work within a biological safety cabinet.
- Participate in the general maintenance of laboratory equipment.
- Conduct aseptic growth and/or manipulation of bacteria, yeast, virus, and mammalian cells.
- Make detailed observations and accurately and precisely record data, summarize data for reports, and document all activities performed in accordance with current Good Manufacturing Practice (cGMP).
- Perform a variety of molecular biology laboratory experiments, tests, and procedures including isolation and analysis of DNA and RNA, PCR, QF-PCR, restriction endonuclease digestion, agarose gel electrophoresis, various blotting techniques, and/or sequencing.
- Report results of experiments, tests, and procedures and analyze data.
- Efficiently organize and plan daily activities.
- Maintain a safe working environment by adhering to company policies and procedures.
- Follow all SOPs, STMs, and cGMP guidelines as they relate to specific tasks.
- Perform all other related duties as assigned.
Requirements
- Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline.
- 0-1 years related experience in a biological lab.
- Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is preferred.
- Must possess excellent interpersonal skills to maintain communication across biological functional groups.
- Able to communicate effectively in a group or one-on-one setting.
- Basic Microsoft Office skills are a plus.
Pay
The pay for this position is $24.70 per hour. Salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
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. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies, and stability and lot release programs, we support 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 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, 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.