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Scientist 1 - Methods Development - Cell & Gene Therapy

Charles River Laboratories International Inc (CRL)

Wayne, PA, US, 19087

Scientist 1 - Methods Development - Cell & Gene Therapy Req ID #:  145710 Location: 

Wayne, PA, US, 19087 For 70 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. Basic Summary  

We are seeking a Methods Development Scientist - Cell & Gene Therapy for our Biologics Testing Solutions site located in WAYNE, PA.

 

You may be required to work a rotating shift schedule that may require weekend hours. Assist in the development of analytical methods to support cell & gene therapy portfolio. Responsible for method development, client interactions, interpretation and reporting of data and regulatory compliance of assigned research projects under minimal supervision. Experience or willingness to learn mammalian cell culture and development of cell-based assays including media preparation, cell counting and passaging. May supervise a limited number of employees involved in the research and development of both internal and Client testing procedures. 

 

The following are responsibilities related to the (Methods Development Scientist - Cell & Gene Therapy): Plan and execute laboratory research and analyze data to design new methods for Cell & Gene therapy clients to generate protocols, and reports (SOPs, STMs) in conjunction with senior research personnel. Use sequence analysis tools and DNA sequence databases to generate oligonucleotide primers and probes for PCR assay development. Collaborate with appropriate departments to coordinate performance of projects, discuss issues, prepare reports, and interact with the clients regarding project design and schedule. May be responsible for personnel activities such as: scheduling, personnel actions (interview and selection of hires, promotions, transfers, etc.). May assist in training and development, including regular direction, coaching and feedback on performance. May assist in preparation and delivery of performance and development plans and salary reviews. May partner with Human Resources for disciplinary actions. May review and approve recorded working time and vacation/time off schedules. May schedule overtime as authorized.  MINIMUM QUALIFICATIONS

  Education:  Ph.D. in a scientific discipline related to cell & molecular biology is preferred. Experience: Minimum of 0-3 years’ experience in a biological research and/or development environment. An equivalent combination of education and experience with contract research or the pharmaceutical industry may be accepted as a satisfactory substitute for the specific education and experience listed above. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Certification/Licensure: None.

Vaccine Mandate

Charles River is a U.S. Federal Contractor.  As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19 by December 8, 2021.  Our main priority is the wellbeing, health, and safety of our people. We will be requiring proof of vaccination from all employees. 

Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

 

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 each and over 200 licenses 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 18,000 employees within 100 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 supported the development of >80% of the drugs approved by the FDA for the past 3 years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin. Veteran or Disability

 

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

 

For more information, please visit www.criver.com.

Nearest Major Market: Philadelphia

Job Segment: Scientific, Biotech, Scientist, Pharmaceutical, Engineering, Science, Research

Job posted: 2022-03-06

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