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Manufacturing Supervisor Jobs

Company

Charles River Laboratories

Address Memphis, TN, United States
Employment type FULL_TIME
Salary
Category Biotechnology Research
Expires 2023-07-25
Posted at 10 months ago
Job Description
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.


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.


Job Summary


We are seeking a Manufacturing Supervisor for our Cell Therapy Manufacturing Business located Memphis, TN.


The following are responsibilities related to the Manufacturing Supervisor:


  • Enforces adherence to regulatory guidelines and Cognate internal policies.
  • Perform other duties, as assigned.
  • Conducts and/or schedules training for new employees including media fills.
  • Advises management on personnel management functions.
  • Schedule’s personnel to support all production related activities.
  • Assures employees understand duties, responsibilities, policies, and procedures.
  • Takes part in Technology Transfer. May collect, analyze and summarize information and trends.
  • Oversees manufacturing personnel in equipment setup, equipment operation, and processes in accordance with cGMPs, Cognate Quality System, and process documents.
  • Leads and implements continuous improvement activities and assists with projects as assigned.
  • Lead, mentor, and develop direct reports.
  • Provides assistance to management in the revision and/or writing of process documents to assure accuracy and completeness. This includes but is not limited to reviewing BPRs and associated documentation for accuracy, compliance, and presence of all verification signatures.


Job Qualifications


The following are minimum qualifications related to the Manufacturing Supervisor position:


  • Must possess effective written and oral communication skills.
  • Must be detail oriented and have excellent organizational skills.
  • Exhibits exceptional leadership qualities.
  • Minimum of an Associate degree required.
  • Must display a high degree of professionalism and confidentiality.
  • 1 year of leadership and/or supervisor experience preferred.
  • Minimum of 3 years of applicable experience.


Compensation Data


The pay range for this position is $74,700 - $83,500. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.


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.


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. Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees.


Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition ([email protected]) 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, 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 [email protected] 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.