QC Analyst Salary at Uamc BETA

Job Description Job Description QC Critical Reagents Associate Location: Novato, CA 94949 (On-site) Assignment: 12-month Assignment with a high potential to extend or convert Shift: M-F / 8:30am-5pm Pay: $26/hour Join a leading pharmaceutical company at the forefront of innovation! We’re looking for a QC Analyst to play a vital role in managing and overseeing the life cycle of critical reagents that power groundbreaking global commercial products. In this exciting, hands-on position, you'll be involved in everything from reagent preparation to inventory management, technical documentation, and ensuring materials are distributed across the global testing network. You’ll make a real impact by supporting cutting-edge research and development, ensuring the quality and stability of materials that are key to successful product outcomes. Key Responsibilities Acquire, prepare, and aliquot critical reagents with precision and care. Lead qualification testing coordination with lab teams to ensur

4 days ago Be among the first 25 applicants Randstad Life Sciences US provided pay range This range is provided by Randstad Life Sciences US. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range $40.00/hr - $41.00/hr Direct message the job poster from Randstad Life Sciences US Scientist | Executive Recruiter _ RLS at Randstad Life Sciences A major company meeting people's needs through innovation, while protecting, renewing and restoring our environment and tackling climate change. We drive science and technology to develop food, beverage and nutritional health products for people and pets. Required: Bachelors degree in food science or equivalent (Microbiology, Engineering) 2-3 years experience in Operations in food industry Interview Process: 1st. Phone Interview 2nd Virtual or In Person Job Description As a Quality Specialist, you will support the Category Mastership strategy by ensuring that our internal documents provide

RESPONSIBILITIES 1. Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices. 2. Execute microbiological and/or analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers. 3. Perform environmental monitoring sampling and testing of facilities, equipment, and utilities. 4. Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports. 5. Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments, and ensure systems for laboratory maintenance are adequate for creating a consistent state of inspection readiness. 6. Assist with monitoring and the control of laboratory supply a

Job Description Job Description Biotechnology company is hiring a Quality Control Analyst for a 12-month contract. Responsibilities Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices. Execute microbiological and/or analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers. Perform environmental monitoring sampling and testing of facilities, equipment, and utilities. Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports. Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments, and ensure systems for laboratory maintenance are adequate for creating a consis

QC Critical Reagents Associate - Pharma 📍 Location: Novato, CA 94949 (On-site) 📅 Assignment: 12-month Assignment 🕒 Shift: M-F / 8:30am-5pm 💰 Pay: $26/hour Join a leading pharmaceutical company at the forefront of innovation! We’re looking for a QC Analyst to play a vital role in managing and overseeing the life cycle of critical reagents that power groundbreaking global commercial products. In this exciting, hands-on position, you'll be involved in everything from reagent preparation to inventory management, technical documentation, and ensuring materials are distributed across the global testing network. You’ll make a real impact by supporting cutting-edge research and development, ensuring the quality and stability of materials that are key to successful product outcomes. Key Responsibilities Acquire, prepare, and aliquot critical reagents with precision and care. Lead qualification testing coordination with lab teams to ensure top-quality standards. Oversee the smooth distributi

Position: Senior Manager, Analytical Quality Assurance Location: Brisbane, CA (Hybrid – 2 days onsite) Length: 9+ months *W2 Candidates Only, No C2C Job Description: Our client is seeking a highly motivated and experienced Senior Manager for their Analytical Quality Assurance (QA) team. This role will support quality control activities in early and late-phase clinical, as well as commercial stage development and production. The Senior Manager will work closely with cross-functional teams including CMC Quality Assurance, Analytical Development, CMC Quality Control, and other departments involved in the development of biologics and small molecules. The ideal candidate will bring a strong background in quality assurance, analytical methods, and regulatory compliance in a CBER/CDER regulated environment. Essential Duties and Responsibilities (but not limited to): Provide QA oversight for analytical method lifecycle activities, including development, validation, transfer, verification, perf

Overview Currently offering a unique opportunity for a QC Professional to join a team with key responsibilities in QC microbiology. Initial duties will include supporting environmental monitoring incubation, reading and reporting of data. Future roles may also incorporate performing environmental monitoring sampling in our CGMP cleanrooms. Other duties include laboratory upkeep, media growth promotion, gram staining and data entry. The qualified candidate will collaborate closely with manufacturing team members and will require working in cGMP cleanrooms and QC labs. Responsibilities • Media growth promotion • Processing of environmental monitoring sampling that include sampling, incubation and reading of media plates • Aseptic gowning qualification • Bioburden • Gram staining • Subculture and coordination of the shipment of isolates for microbial identification • Gas testing • Raw materials sampling and testing • Equipment cleaning and maintenance • Laboratory upkeep and inventory man

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