Director, Quality Salary at Controlup BETA

Director, Quality Operations Fremont, CA, US Requisition ID: 4508 Salary Range:$154,794.00 To $232,190.00 Annually DESCRIPTION: The Director of Quality Operations is responsible for the planning, leadership and operational execution of the organization's quality departments at the site level as well as customer and supplier quality support teams. This is a highly visible and customer facing role critical to the growth and success of the company. As the quality representative on the executive staff, responsibilities include development of overall quality strategy, goals, and plans to achieve them. Oversee and coordinate quality system and quality control efforts across company facilities to which they are responsible. Drive cross-functional continuous improvement efforts to meet and exceed customer expectations. Make critical, creative and strategic decisions as a result of analysis of available information including risk-assessment for the business. ESSENTIAL DUTIES: • Leads the compan

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

Regulatory & Quality Leadership Opportunity - Drive Innovation in Biopharma! Are you a seasoned Quality and Regulatory professional ready to take on a pivotal leadership role within a dynamic and growing biopharmaceutical organization? Our client, a cutting-edge company focused on advancing groundbreaking therapies, is seeking a highly skilled and experienced Director/Senior Director of Quality and Regulatory Affairs to join their team. What You'll Do: Strategic Quality Oversight: Spearhead supplier selection and audits, lead internal, client, and regulatory audits, and drive Quality Management and Review Board meetings. Risk Mitigation & Collaboration: Collaborate with cross-functional teams to identify and mitigate potential quality and regulatory risks, ensuring seamless operations. Regulatory Submissions & Compliance: Plan, prepare, and manage regulatory submissions (INDs, NDA/BLAs) in partnership with client stakeholders. Maintain regulatory registrations and licenses, ensuring co

Job Description San Ramon Regional Medical Center San Ramon Regional Medical Center began serving residents of the San Ramon Valley and its surrounding communities in 1990. Located on a hillside overlooking the valley, we are a 123-bed, acute-care hospital, primary stroke center, and a cardiac heart surgery hospital. San Ramon Regional Medical Center provides comprehensive inpatient and outpatient services. Personalized service and a patient-centered philosophy are distinctive qualities of our facility. We offer competitive salaries and benefits including a matching 401(k), several health & dental plans to choose from, generous tuition assistance plans, and relocation assistance for select positions. Comprehensive benefits for medical, prescription drug, dental, vision, behavioral health and telemedicine services Wellbeing support, including employee assistance program (EAP) Time away from work programs for paid time off, long- and short-term plan coverage Savings and retirement includ

Director, QA Compliance Our client is a clinical stage biotech that is seeking a Director of Quality Compliance to lead GCP quality systems and ensure compliance with US, EU, and global regulations. This role will oversee quality processes including policies, SOPs, deviations, change control, CAPAs, document control, training, and vendor audits. Responsibilities include building and managing the quality management system, supporting clinical and future commercial activities, leading system implementations, and ensuring inspection readiness. Requirements: Bachelor’s or Master’s in a scientific field with progressive experience in biotech/pharma clinical quality Strong knowledge of GCP QA regulatory requirements and quality systems Experience developing and managing quality processes Risk management, root cause analysis, and inspection support experience Excellent communication, project management, and organizational skills Up to 20% travel Please send resume to sarah.viall@meetlifescien

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

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 Pharmacovigilance Quality Assurance is a senior member of the CQA team. The Director will lead

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