QC Analyst Salary at Wynne Systems Inc BETA

Job Title: Quality Analyst Job Description We are seeking a detail-oriented QC Analyst to join our team. The role involves testing using PCR and SDS-Page, validating assays, managing change controls, conducting stability and raw material testing, and maintaining thorough documentation. The QC Analyst will also oversee a team of 4-6 people and provide team leadership. Hard Skills + Validating assays + Method Development + Testing using PCR + Testing using SDS-Page + Managing change controls + Stability testing + Raw material testing + Documentation Soft Skills + Team leadership + Attention to detail + Strong communication skills Work Site This is a fully on-site position in Los Angeles, California. Work Environment Working in an office and lab setting About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, inno

Job Description Job Description Duties and Responsibilities: · Request Vendor Qualification documentation. Organize and update them. · Manage raw materials and packaging components qualification program · Create codes for raw materials and packaging components · Create raw materials, packaging components specification and testing report · Verify shipment against Packing Slip, BOL, CoA, and/or CoC · Enter information associated with the materials received into ERP · Follow the company testing policies corresponding to Vendor Qualification program · Special projects and other duties assigned. Work Experience/Qualifications: · Experience in Dietary Supplements, Cosmetics, Pharmaceutical, or Food Industry preferred · Working knowledge of applicable safety and standard guidelines such as SOP, cGMP, GLP, and MSDS · Good interpersonal skills · Strong computer skills · Ability to work independently and in a team environment. · Ability to follow instructions · Good attendance and punctuality ·

Job Description Job Description The Quality Control Analyst is responsible for reviewing and auditing funded loans to ensure adherence to company underwriting policies, regulatory requirements, and industry standards. They will compile reports on the findings and collaborate with Sales, Credit/Risk, Operations to resolve the findings. This role also involves working with third party diligence and audit firms to deliver files, respond and satisfy any findings. ESSENTIAL FUNCTIONS include the following. Other duties may be assigned. Conduct detailed reviews of funded loans to ensure accuracy, completeness, and adherence to company policies and regulatory requirements. Create and maintain Quality Control reports. Prepare detailed reports summarizing findings from loan reviews, including identified deficiencies and determine corrective actions. Report, escalate discrepancies to appropriate business units for resolutions/clarification. Maintain accurate records of all reviews, findings, and

At top Biopharmaceutical company, we're transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Quality Control Analyst I at our Los Angeles, CA site. Here, you will be a vital contributor to our inspiring, bold mission. Summary: Under supervision, the Microbiology QC Analyst, is responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, final produc

Job description Sr. Quality Control Analyst is responsible for overseeing all aspects of FlexPoint Inc’s QC Department, QC processes (pre-funding, post-closing, discretionary, etc.), QC Reporting, and QC systems to ensure high-quality loan production and compliance with regulatory, investor, and agency requirements. This function will provide guidance and training to ensure the integrity of FlexPoint’s QC review process and loans. This position also involves significant interaction with internal and external stakeholders, including auditors, agencies, and regulators, regarding, among other things, QC findings, QC policies and procedures, and third-party findings. Responsibilities: Develop, implement, and maintain comprehensive QC policies and procedures that align with industry best practices, regulatory requirements, and agency/investor guidelines. Ensure QC reviews and QC reports are completed and delivered in a consistent and timely manner. Ensure QC reviews and QC processes comply

Job Description Job Description The Quality Control Analyst is responsible for conducting the cell-based potency assays (CBPA) of biologics for release and stability of both commercial and late-stage biologics under current good manufacture practice(cGMP). He/She will prepare all documentation associated with the cGMP testing and independently or in a team setting execute protocols in support of manufacture of our biologics product. The position is responsible for cGMP compliance of the quality control CBPA laboratory, ensuring that all cell Based Potency Assays testing is performed according to the FDA, foreign MOH and our requirements. Major Responsibilities: Perform cGMP testing in support of the manufacture of our biologics products. Generate, compile, and evaluate data for technical reports to support commercial and clinical supplies. Review and approve raw data and laboratory logbooks/worksheets. Perform cell culture and cell banking. Manage critical reagents and supplies. Write

Job Description Job Description We have an exciting opportunity to partner with a well established Food Processing company in Riverside, CA that is currently seeking Quality Assurance Analyst. Job Summary: The Quality Control Analyst will monitor plant processing operations and programs relating to food safety, HACCP, and regulatory compliance. This role will perform a variety of technical inspections and testing to detect processing, manufacturing, or other defects, and ensure that all products meet our stringent quality and food safety standards. Direct Placements Payrate: $19-$22/hr. based on experience Schedule: Monday- Friday (some Saturdays if needed) 4:00 PM-4:00 AM (10-12 hrs shifts) Key Responsibilities: Perform quality inspections of products before public release to ensure they meet food safety regulations and internal standards. Operate under Good Manufacturing Practices (GMP) and be familiar with the HACCP system. Observe and report all food product deficiencies promptly.

Innova Solutions has a client that is immediately hiring for an Assembly Rework Technician Position type: Full Time, Contract Duration: 10+ months Location: Irvine, CA, 92618 SHIFT: 5 AM to 1:30 PM with OT available As an Assembly Rework Technician, you will: Performs Manufacturing operations in accordance with the associated documentation and the time allocated, using the resources available Is responsible for complex work and rework at unit and component level Chooses and implements suitable methods, resources, and procedures. Brings support to the operators. The ideal candidate will have: 4 years working in an industrial manufacturing environment A min of 3 years working in a Quality Assurance or Quality Control department Has performed process and/or quality system audits Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. We are currently interviewing to fill this