QA Assistant Salary at Lelo 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 Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perfor

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

Director of Quality Assurance & Regulatory Affairs Location: San Francisco Bay Area Compensation: Competitive salary, benefits, and equity/stock options About the Role: A well-funded MedTech startup developing AI-driven medical imaging solutions is seeking a Director of Quality Assurance & Regulatory Affairs. This role will lead Quality and Regulatory functions, ensuring FDA compliance and driving a successful 510(k) submission. The ideal candidate will bring deep experience in medical device development and a strong technical background. Key Responsibilities: Develop, implement, and oversee the Quality Management System (QMS) in compliance with FDA, ISO 13485, and other standards. Lead quality processes, including design control, risk management, and CAPA. Develop and execute regulatory strategies for FDA 510(k) submissions. Ensure compliance with medical device regulations throughout product development. Collaborate with R&D, Operations, and Product teams to align quality and regulat

Overview: AngioSafe is a Bay Area start-up focusing on improving healthcare delivery through state-of-the-art catheter development. Our seasoned experts are committed to producing and selling high quality and innovative products to decrease risk and improve outcomes of arterial disease. The Quality Assurance position is responsible for the support and performance of QA/QS functions/activities and adherence to applicable regulatory standards for medical devices. Roles & Responsibilities: Support the development and maintenance of the Quality Management System (QMS), ensuring that corporate operations are aligned with applicable regulations Serve as system administrator for MasterControl Electronic Document Management and Training System (EDMS), including responsibility for configuration, user training, account management, training course creation and assignment, and assessment of upgrades and patches. Ensure validated course creation and assignment, and assessment of upgrades and patche

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

We are hiring a Full Time / Direct Hire Bilingual Mandarin Quality Manager in San Jose, CA. This company has Global locations and seeking Bilingual Mandarin Quality Manager to work with their Mandarin Speaking team. Quality Manager • Responsibilities: o Oversee QA operations, including inspections, supplier management, root cause analysis, and product reliability. o Develop and maintain quality management systems, including training programs. o Lead internal audits and external certifications for compliance with industry standards. o Drive quality improvement initiatives and manage customer complaints with preventive measures. o Engage clients through regular quality meetings and action plans. o Lead and develop the QA team, fostering accountability and continuous improvement. Qualifications: o Experience: 5+ years in QA, including 3+ years in management. o Education: Bachelor’s degree in Engineering, Math, or related fields. Skills: o Strong analytical and problem-solving abilities. o

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

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