Quality Control Salary at Nexus BETA

Job Description Job Description Ideal candidate should have automotive Knowledge or body shop experience. Must be able to work in a fast paced environment, Ability to be a team player and assist others as needed, Ability to work independently and responsibly, Duties consist of Clean Parts-Using hand / or air tools as well as some cleaning agents, be able to identify and retrieve parts from warehouse locations, Inspect parts-verify description and insure parts are in good working order, Prepare parts for delivery, Maintain a clean work environment. Company Description Brandy Brow Auto Parts, inc.was established in 1937 and has been improving ever since! we offer acres of foreign and domestic vehicles,Our facility which is open to the public is environmental friendly,organized and well maintained, we are open 6 days a week and we offer lifetime warranties on our parts and it's a fun place to shop. Company Description Brandy Brow Auto Parts, inc.was established in 1937 and has been improv

Job Description Job Description · Maintain all USDA, FDA, State Health and OSHA standards at all times. · Support management updates and maintenance of the quality management system. · Support audits implementation of the quality system · Support Manages requests for, and follows up on, corrective actions · Calibrates measuring and test equipment · Ensures proper sanitary conditions in all facilities · Performs inspections, and testing in accordance with quality plan and verifies compliance. · Execute the re-inspection process of nonconforming products · Support maintenance of USDA/ISO/FDA/OSHA documentation · Assures compliance with OSHA regulations · Identifies training needs and assures training for all personnel (Quality/OSHA) · Verify compliance of all HACCP/ISO Documentation · Conduct ISO/HACCP meetings · Manage all Quality Control and Sanitation personnel. · Manage and execute daily SSOP as required via USDA · Additional tasks - as needed - not described in this task description

Quality Control Analyst - Contract - Cambridge, MA Proclinical is seeking a Quality Control Analyst for a contract role in Cambridge, MA. Primary Responsibilities: The successful candidate will be responsible for ensuring the completeness, consistency, and accuracy of regulatory filings, laboratory data, and reports. This role offers flexibility for remote work, with some on-site presence expected. Occasional travel to CMO/CTL sites may also be required. Skills & Requirements: Degree in chemistry, biology, biochemistry, or a related scientific field. Experience in a GMP Quality Control function within the pharmaceutical/biotech industry. Knowledge of method transfer and analytical method implementation. Strong technical writing skills, particularly for investigations. Proficient in data analysis and interpretation with excellent attention to detail. Solid problem-solving skills and experience in conducting investigations and implementing CAPA. Strong organizational skills with the abil

QC Associate Responsible for managing and executing QC activities in support of product(s) production, release, and stability. Ensures GMP activities are conducted in accordance with applicable SOPs, compendia, approved methods, and in accordance with companys and regulatory agencies policies and procedures Key Duties and Accountabilities Manage QC data of multiple programs through external/third party suppliers (CDMO, CTO, etc.) Perform raw data review of third-party release and stability testing data Perform trending for release, and stability using applicable software (JMP, iStability, Graphpad, etc). Draft and review QC documentation including Stability Protocols and Reports, SOPs, Material specifications, CoA templates and other quality documents. In collaboration with Analytical Development, support method qualification, fit for use, validation and method transfer activities Support reference standard program Draft and execute quality systems (e.g., OOS/OOT, Deviations, Change Co

Job Description Job Description Kirwan Surgical Products LLC is a medium-sized company located in Marshfield, MA. We specialize in the development of superior products for microsurgical specialties including ophthalmology, ear, nose, and throat, plastic and reconstructive surgery, and orthopedic surgery. We are currently seeking qualified candidates for a Quality Control Inspector to join our team. The Q.C. Inspector inspects medical devices in a controlled environment. Prior Incoming QC experience is highly preferred. Key Responsibilities: A typical day consists of inspecting and testing products, ordering labels, and washing products. Assure that all parts produced comply with documented company and customer quality standards. Report and record any nonconforming products. Look for ways to improve and promote quality, and demonstrate accuracy and thoroughness. Learn to comprehend technical terminology, as needed in interpreting Engineering drawings and specifications. Ability to adequ

qPCR experience is required. Job Summary/Operations Involvement: Primary Duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations /validation/or development studies. Testing may include but not limited to samples from drug substances and drug product manufacturing, stability and various protocol studies using approved test methods or test methods derived from QC technical protocols. Specific Biochemistry Focus Areas: Product Testing: Area focuses on techniques such as SDS-PAGE Silver, QPCR, Potency, Kinetics assay, Enzyme Activity, pH, Osmo, A280 etc., in order to support in-process, release and stability testing. Role supports commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation. The introduction of new equipment and technology to improve sustainability and compliance is expected. Job Function and description 40-50% Testing execution, participate in tra

Are you ready to inspect your way to success? Advantage Resourcing is excited to partner with a reputable manufacturing company in Rumford, RI, as they seek a dedicated Quality Control Inspector to join their team. This organization prides itself on precision, teamwork, and continuous improvement, ensuring that every product meets the highest quality standards. If you have a keen eye for detail and a passion for excellence, consider becoming a vital part of a company that truly cares about its employees and customers. Pay: $17.25/hr 3rd Shift: 4:00 PM - 4:00 AM | Monday - Friday Requirements: High school diploma or equivalent required Technical training or certifications in quality control are considered a plus. Experience in a manufacturing or production environment, particularly in a quality control role, is essential. Ability to interpret and follow technical documents, blueprints, and quality standards Proficiency in using basic inspection tools, such as magnifiers and calipers, is

Job Title: Quality Control Bioassay and Virology Operations Lead Position Summary: This role is responsible for the daily management and operations of the QC Bioassay and Virology Testing team within the QC Operations department, supporting clinical and commercial AAV-based products. Key responsibilities include overseeing cGMP processes such as in-process, lot release, stability, and raw material testing. The role also involves managing quality systems, including deviations, CAPAs, OOS, change controls, and data integrity, as well as supporting audit readiness and ensuring team training. The position includes managing, coaching, and developing a team of 4+ analysts across various experience levels. Key Responsibilities: - Maintain a compliant, efficient, and safe cGMP laboratory in accordance with regulatory, site, and corporate standards. - Manage daily QC operations for cGMP routine and non-routine testing of in-process samples, drug substances, final products, virus banks, and cell