Supervisor, QC Salary at Kasper BETA

Microbiology Laboratory Technician Corporate Statement Nephron Pharmaceuticals Corporation is a privately owned global leader in the manufacturing of generic drug products, over-the-counter (OTC) drug products and medical devices. Nephron's products are sterile, preservative and additive free and proudly made in the USA! We are headquartered in West Columbia, South Carolina, with additional distribution centers in Kentucky and Arizona. Our location provides the ability to develop new devices and medications including respiratory therapies, ophthalmics, and injectables, for in-house or contract manufacturing opportunities. The facility utilizes completely automated manufacturing, packaging, and distribution systems, in addition to high volume and redundant utility systems, to ensure production system availability. Nephron specializes in Blow-Fill-Seal (BFS) manufacturing, a niche technology that allows a vial of medication to be formed, filled and sealed in a continuous process, in a st

Overview: The work we do at FDB has never been more importantand we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in peoples lives. Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what FDB call Genki. External US: College Station, Texas may be a small, university town, but the lively cultural scene and local amenities make it a great place for families as well as those who want the ease of small-town life and the convenience of living close to the vibrant pulse of big cities. Eighty-seven percent of Texas' population lives within a 180-mile radius, so we are in the center of it all in Texas. And our site is nestled in the hub of innovation, repre

This is a 2nd shift opening. Relocation lump sum and sponsorship for US based candidates will be considered. The QC Supervisor, Cell Biology will be responsible for coordinating the installation and qualification of new analytical equipment in support of GMP release and stability testing. The Cell Biology/Immunology Supervisor will lead tech transfer activities of qualified cell based and immunological methods from designated donor laboratories. The Supervisor will play a pivotal role in selecting qualified personnel to staff the QC Cell Biology laboratory. Work Location - College Station, TX College Station, Texas may be a small, university town, but the lively cultural scene and local amenities make it a great place for families as well as those who want the ease of small-town life and the convenience of living close to the vibrant pulse of big cities. Eighty-seven percent of Texas' population lives within a 180-mile radius, so we are in the center of it all in Texas. And our site is

Quality Assurance / Quality Control Supervisor Shift/Hours: Monday - Friday Pay Rate: $75,000+/annually Location: Fairfield, NJ 07004 Experience: Manufacturing or Production Environment Summary: PrideStaff is working with an Innovative global pharmaceutical manufacturer to hire a QA/QC Supervisor. We are seeking a dedicated and detail-oriented QA/QC Supervisor to join our team in Fairfield, NJ. The ideal candidate will be responsible for overseeing the Quality Assurance and Quality Control functions within our pharmaceutical manufacturing environment. This role is crucial in ensuring compliance with industry regulations and maintaining the highest standards of product quality. If you are a motivated individual with a passion for ensuring product quality and compliance in the pharmaceutical industry, we invite you to apply now! ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Position Summary: Assures that our facility and our employees are compliant with FDA Regs 21CFR 111- cGMP’

Kelly Science is seeking an Overnight QC Supervisor for a growing food and beverages company located in Schenectady, NY. Salary: $60,000-65,000/year depending on experience Shift: Tuesday-Saturday Overnight hours Employment Type: Full Time; Direct Hire Summary: As the Overnight QC Supervisor, you will be responsible for supervising a quality team of 12 individuals ensuring total package/package quality, cost management, safety and compliance with GMP standards, and executing all QA/QC protocols to ensure Plant Quality service objectives are met. Job Responsibilities: Providing supervision of laboratory / water treatment / syrup blending / sanitation / microbiological equipment, raw materials, quality processes and people in a food production/packaging environment. Optimizing resources while ensuring raw materials and finished product meet specifications and manufacturing standards and in accordance with FDA, CFIA, USDA, GMP’s HACCP, and all other governmental policies, procedures, and

NEW Quality Coordinator Opening at one of the nation's leading integrated healthcare networks! This organization has been recognized for its dedication to innovation as well as been awarded a "Laboratory of the Year." This laboratory provides testing services including (but not limited to) hematology, chemistry, serology, histology, molecular biology, next generation sequencing and MORE! This well-established organization is looking to add a permanent and full time Quality Coordinator to their team on either day shift. In this position the Quality Coordinator will be responsible for all quality control procedures and comply with quality assurance and quality management standards as outlined by JCAHO, CAP, CLIA and other applicable agencies. Required: Bachelors or Associates Degree in Medical Technology (or related field) Required: ASCP or AMT Certification as a Medical Technologist (MT) OR Medical Laboratory Scientist (MLS) or Medical Laboratory Technician (MLT) This facility is offeri

Job Title: Quality Control Supervisor Overview: We are looking for a skilled Quality Control Supervisor to lead and manage the quality processes for our products. This role focuses on ensuring high-quality standards from raw materials through to final products, overseeing testing, regulatory compliance, and team management. Key Responsibilities: Quality Oversight: Supervise daily QC operations, ensuring testing, inspections, and procedures meet industry standards. Testing & Inspections: Oversee raw material, in-process, and finished product testing; ensure equipment calibration and environmental monitoring. Team Leadership: Lead and mentor a small team, fostering development and ensuring effective workload management. Regulatory Compliance: Ensure compliance with FDA and GMP standards; maintain up-to-date knowledge of relevant regulations. Problem Resolution: Investigate quality issues and implement corrective actions, working cross-functionally to drive continuous improvement. Qualifi

Job Description The Quality Control Compliance Coordinator ensures that the radiology team complies with standards set by local, state, and federal regulatory and accreditation agencies. They oversee the interpretation of standards and preparation for surveys. The coordinator also manages compliance-related tasks and maintains quality control programs for Radiology, Interventional Radiology, Nuclear Medicine, CT, MRI, and Ultrasound. Under general supervisor, will collaborate closely with the Director/Manager and Radiation Safety Officer. Responsibilities Verify that all quality control activities are carried out in accordance with standard operating procedures and policy Create a strategy to guarantee preparedness and a system of checks and balances to evaluate adherence to any survey (such as ACR, TDH, TJC, CMS, etc.). Assist the Radiation Safety Officer in completing mandatory quality control tests and evaluations on a daily, weekly, monthly, and annual basis Review all modality (CT