Quality Assurance Specialist Salary at Atia Vision BETA

We have an outstanding career opportunity for a Quality Assurance Specialist II to join a leading Company located in the Concord, CA surrounding area. Salary: $80,000 - $85,000 Job Responsibilities: Responsible for leading the site's quality control activities and requirements for production products and processes. Lead and/or work with others to drive continuous improvement and best-in-class execution that maximizes customer satisfaction through world-class, on-time delivery. Work closely with the Product Quality engineer. Provide guidance from a quality perspective, as well as customer requirements and standards, and perform audits. Handle any production and product related quality issues. Guide manufacturing team as per customer requirements and IPC / IATF standards. Working closely with the manufacturing team to ensure product quality and train operators as and when needed for quality requirements. Responsible for performing Out of Box audits. Maintain equipment Calibration. Provid

About Us: Nkarta?is a publicly traded (Nasdaq?symbol?NKTX), biotechnology company headquartered in South San Francisco focused on the discovery, development and manufacturing of off-the-shelf, natural killer (NK) cell therapies. Our near-term goal is to bring cell therapy out into the community setting, dramatically expanding access for patients. Founded in 2015 at the birthplace of biotechnology, Nkarta is a fast-growing, fast-moving, clinical-stage company that has built an extensive cell therapy manufacturing operation in anticipation of product commercialization. Our developmental pipeline of engineered NK cell therapies includes clinical programs in B-cell malignancies and autoimmune diseases. Complementing our broad research and development capabilities, Nkarta has also built an extensive cell therapy manufacturing operation. We recently built out a 23,000-square foot clinical good manufacturing practice, or cGMP, facility on-site at our primary corporate location in South San Fr

Discover International are currently partnered with a leading Pharmaceutical Company based around 30 Minutes from San Jose, CA who are seeking a Quality Assurance Specialist to be work fully onsite. This role will be an 18 Month Contract. **Please only consider applying if you are located within this area and happy to work onsite** Key Responsibilities: Quality Control (QC): Conduct routine and non-routine testing of raw materials, in-process samples, and finished products to ensure compliance with specifications. Manufacturing Support: Collaborate with production teams to identify and resolve quality issues during the manufacturing process. Batch Release: Review and approve batch records for product release, ensuring all manufacturing and quality control steps have been completed per regulatory standards. LIMS (Laboratory Information Management System): Utilize LIMS to manage and track laboratory data, ensuring all information is accurate and up-to-date. Lab Work: Perform lab testing

Summary See below for important information regarding this job. Additional vacancies may be filled from this announcement. Responsibilities Performs duties associated with the administration of the quality assurance provisions of contracts by designing, implementing, and maintaining a risk-based surveillance program and assessment plan. Identifies opportunities for process improvements through analysis of process measurement data. Serves as a member of a multi-functional or technical team. Responsible for implementing the overall Quality Program for a diversity of products and services in support of U.S. Government acquisition at one or more suppliers facilities. Ensures contractor compliance with all requirements related to the design, manufacturing, repair, overhaul, and modernization of a variety of items for contractor and customer activities throughout the world. Independently performs audits/surveillance of contractors processes to ensure customer and contractual requirements are

Job Title: Quality Assurance SpecialistJob Description We are seeking a dedicated Quality Assurance Specialist to manage and investigate product quality complaints. The role involves documenting complaints, supporting investigations, ensuring compliance with regulatory requirements, and maintaining high-quality standards in adherence to Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs). The specialist will also perform data analysis, manage product complaint samples, and support corrective and preventive actions (CAPA). Responsibilities + Receive product quality complaints. + Document complaints in the Quality System and triage safety events to the appropriate department. + Support product quality complaint investigations. + Ensure compliance with applicable regulatory requirements. + Maintain programs and processes to ensure high-quality products and GMP/GLP compliance. + Perform data analysis to support complaint investigations and quarterly trend analysis. + A

Responsibilities: The Specialist IV supports compliance for operational functions at Revance, focusing on technical writing and quality system records (e.g., laboratory investigations, deviations, CAPA, change controls). Responsibilities include conducting investigations, analyzing operational metrics, authoring controlled documents, and ensuring compliance with training programs. Strong understanding of data integrity and risk analysis is essential. Prolonged sitting and computer work, ability to lift up to 10 pounds Requirements: GMP Compliance Technical Writing Laboratory Investigations Deviation and CAPA Management Change Control Root Cause Analysis Data Integrity Analytical Techniques (ELISA, SDS-PAGE, Western Blot, Karl Fischer, HPLC)

List Lab’s mission is to “harness bacteria’s potential for a healthier world.” We are a premier contract development and manufacturing organization for bacterial derived products for early clinical trials including live biotherapeutic products derived from the rapidly growing microbiome field. Live biotherapeutic products, an exciting new therapeutic, are a novel approach to disease treatment and have significant potential to improve patient lives. List Labs also specializes in the production of both native and recombinant bacterial proteins and toxins used for research and development. List Labs offers a dynamic and congenial company environment and the convenience of working in the South Bay Area. We are seeking a talented and motivated Quality Assurance Specialist to support our Quality and Compliance Department. This position will be primarily responsible for GMP product support, and administering quality systems such as supplier qualification, deviations, CAPAs, and change control

Job Title: Sr. QA Specialist Location: South San Francisco Industry: Medical Device Style: Hybrid Length of Contract: Initial 6-12 Months with potential extension Job Summary The Senior Quality Systems Specialist is responsible for managing and supporting the Quality Management System (QMS), including areas such as document control, training, CAPA (Corrective and Preventive Actions), internal and supplier audits, nonconformance management, and assisting with production-related tasks such as incoming inspections, rework, and deviation handling. This role also involves planning and supporting quality-related projects to align with company objectives. Essential Responsibilities CAPA Management: Oversee all CAPA processes from initiation and investigation to implementing corrective actions, verifying effectiveness, and closing CAPAs. Internal Audits: Manage the internal audit schedule, lead or facilitate audits, and ensure findings are addressed and resolved. Support external audits of the