This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

QC Supervisor

Charles River Laboratories International Inc (CRL)

Charleston, SC, US, 29407

QC Supervisor Req ID #:  193751 Location: 

Charleston, SC, US, 29407 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. Job Summary  

We are seeking a QC Supervisor for our Microbial Solutions site in Charleston, SC. 

 

Responsible for supervising environmental monitoring of LAL (Limulus Amebocyte Lysate) and Crude Lysate production areas to ensure appropriate conditions are maintained. May help managing the quality and integrity of product by testing incoming materials, excipients and final product. Oversee Crude Lysate recovery procedures during the Bleeding Season.

  Perform and document the training of new Quality Control employees on all laboratory test methods. Maintain Environmental Monitoring System sampling sites, readings and reporting as it applies to production fills and routine sampling. Compile data for environmental monitoring for management review meetings. Responsible for completing and reviewing paperwork associated with lab investigations and exception documents. Oversee the scheduling of laboratory functions to ensure timely product release. Ensure the Quality Control staff collects samples from production lots to ensure Quality Control testing and Retention storage requirements are met. Oversee and Evaluate media via Growth Promotion testing. Responsible for final Review of Quality Control data and environmental monitoring Manage, develop and review Controlled Documents such as Standard Operating Procedures and Specifications. Responsible for execution of and writing of protocols. Perform Internal Audits. Serve as point of contact with customers to support customer audits hosted by Quality Assurance Supervise staff and approve time off, maintain time cards and monitor performance and manage staff performance appraisal review program. May help with Quality Control release testing of finished products including but not limited to potency, sterility, moisture, pH, endotoxin testing, precision, and accuracy. May help with Quality Control release testing of incoming materials and supplies; formulation excipients; final LAL and accessory products. Compliance with Standard Operating Procedures, Specifications and Good Manufacturing Practices must be met. May help to perform testing to support the long-term stability program. Perform other related duties as assigned. Job Qualifications

  Education: Bachelor’s degree (B.A. /B.S.) in Microbiology Biology. Experience: Three to Five years experience with GMP products preferred. Prior experience with laboratory operations and auditing preferred. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Other: Computer literacy must include word processing, spreadsheet and advanced math skills. Attention to detail in all aspects of work is essential

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 17,000 employees within 90 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. And in 2019, revenue increased to $2.62 billion.

 

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 ~85% of the drugs approved by the FDA in 2019.

 

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

 

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: Charleston South Carolina

Nearest Secondary Market: South Carolina

Job Segment: Pharmaceutical, Quality Assurance, Biology, Biotech, Microbiology, Science, Technology

Job posted: 2022-09-29

3