Quality Assurance Associate Salary at Upstartother BETA

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing's syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. The Manager of Clinical Quality Assurance position is an exciting opportunity to build upon solid clinical r

Are you a detail-oriented professional with a passion for quality assurance and compliance in the pharmaceutical or biotechnology industry? Adecco is seeking a **_Quality Assurance (QA) Associate_** to join their clients team in **_Concord, CA_** . **_Job Opportunity: Quality Assurance Associate $20.00/HR + Benefits_** **_Location: Concord, CA_** **_Why work with Adecco:_** + **_Pay is $_** 25.00/HR. (20.00/HR.) + **_Benefits, including health, dental, vision, and 401k._** **_What youll do:_** Ensure compliance with data integrity standards under **21 CFR Part 11, 210, and 211** . Maintain and manage **QA files, training matrices** , and other essential records. Review **Certificates of Analysis** , raw data files, in-house documentation, and logbooks for accuracy and completeness. Scan, submit, and archive data and certificates to clients efficiently. Manage **document control** and participate in **quality event investigations** using **eQMS MasterControl** . Provide support for **cl

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing's syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. The Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perfor

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

This is a 12-month contract. Shift: Alt Wednesday, Thursday-Saturday 6:00AM-7:00PM Responsibilities: Provide on-the-floor Quality Assurance oversight and support to manufacturing operations. Review executed batch records and associated documents to ensure compliance with approved procedures and cGMP expectations. Respond to quality-related incidents or non-conformances on the floor and secure necessary documentation for real-time investigations. Represent Quality Assurance in support of deviations including active participation in Root Cause Analysis (RCA). Provide cGMP and compliance guidance to Manufacturing and Technical Services personnel. Provide Quality Assurance support including authoring, review, and approval of documents in Quality Management Systems in accordance with company policies. Perform area walkthroughs. Perform other duties and projects as assigned by management. Qualifications B.S. in scientific discipline or equivalent work experience. Prior batch record execution

Job Description Job Description Company Description Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading biologics analytical organization with operations in the San Francisco Bay Area and New Jersey. We specialize in bioanalytical and CMC analytical services for biotech and pharmaceutical companies developing biologics. Our expertise spans a wide range of therapeutic modalities, supporting projects from discovery through clinical development. Role Description Reporting directly to the CEO, the Director of Quality Assurance (QA) will be responsible for the development, management, and continuous improvement of quality systems ensuring compliance with Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), and other applicable regulatory standards for our bioanalytical GLP lab in Pleasanton, California. This role ensures that facilities, equipment, personnel, and procedures meet all regulatory requirements and effectively supports nonclinical and clinica

Job Title: Quality Assurance Coordinator Job Location: San Jose-USA-95110 Work Location Type: On-Site Salary Range: $18.53 - 28.14 per hour About us LSG Sky Chefs is one of the world’s largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted “Airline Caterer of the Year in North America” for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America. Role Purpose Statement Primary responsibility is to maintain the “Global Quality System” of LSG Skychefs and LHI to ensure the Customer Service Center (CSC) is in compliance with customer, Federal Drug Administration (FDA), US Department of Agriculture (USDA), and Seafood Hazard Analysis and Criti

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Sr. Specialist Quality Assurance Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bach