Supervisor Methods Development

Supervisor Methods Development Req ID #:  205357 Location: 

Wayne, PA, US, 19087 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.

IMPORTANT:   In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process.  Please make sure work history and education are added correctly.   

  Basic Summary We are seeking a Supervisor-Methods Development for our Biologics Testing Solutions site located in Wayne. 

You may be required to work a rotating shift schedule that may require weekend hours.

Looking to hire an experienced laboratory Supervisor with good communications and technical skills in molecular biology to support the Methods Development team engaged in the design and development of new analytical test methods 

ESSENTIAL DUTIES AND RESPONSIBILITIES: Supervise daily laboratory activities and ensure compliance and excellent service to our clients by training technical personnel in general laboratory skills and concepts of GMP. The laboratory Supervisor will help revise documents/SOPs, address audit findings, maintain departmental budgetary responsibilities to ensure the methods development laboratory maintains its compliance status Assist in laboratory work associated with the development of PCR and cell culture-based assays, whenever necessary. Schedule and provide daily supervision and review work of assigned departmental employees to ensure accuracy and adherence to departmental policies, practices, and procedures [SOPs, safety procedures and biosafety protocols].   Identify training and development needs for Methods staff, own the development, implementation, and delivery of departmental training programs. Ensure that direct reports receive departmental orientation and necessary on-the-job training. Initiate discussions with department leadership and employees to recommend regular coaching and counseling to ensure that analyst can reach their career goals and aspirations.   Recommend staffing requirements, promotions and raises and partner with human resources and department management. Assist in monitoring performance of direct reports and handling of any emerging disciplinary issues or concerns. Assist in the development of a departmental backup plan and succession planning of key technical personnel. 

MINIMUM QUALIFICATIONS:

  Bachelor's degree (B.S./B.A.) or equivalent in biology or a related discipline. Minimum of 2-4 years related laboratory/supervisory experience. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Demonstrated leadership skills required. Working knowledge of cGMP or regulatory affairs pertaining to the pharmaceutical and biotechnology industries required.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. 

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 20,000 employees within 110 facilities in 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 86% of the drugs approved by the FDA in 2021.

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 status.

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

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