Quality Assurance Lead Salary at Xyicon BETA

At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the industry. Every day, 80,000 colleagues lead the way to greener and smarter mobility worldwide, connecting cities as we reduce carbon and replace cars. Could you be the full-time onsite Project Quality Safety Manager in Vallejo, CA, US we're looking for? Your future role Take on a new challenge and apply your comprehensive engineering and management expertise in a new cutting-edge field. You'll work alongside diligent, innovative, and collaborative teammates. You'll ensure project excellence by upholding the highest standards of quality and safety. Day-to-day, you'll work closely with teams across the business (Engineering, Industrial, Supplier Management), establish and implement the Project Quality plan, and much more. We'll loo

Director, GCP QA Compliance Our biotech partner is a well-established, commercially successful clinical stage biotech that is seeking a Director of Clinical Quality Assurance to lead the CQA function and build/manage a team. This role will oversee CQA strategy across policies, SOPs, deviations, change control, CAPAs, and vendor audits. This is a great opportunity for a Clinical QA leader to help progress a robust pipeline of therapeutics across oncology, neurology, endocrinology, and more areas. This position will be 3 days onsite in Redwood City, CA. Responsibilities: Lead Clinical Quality Assurance as a manager to the CQA team supporting various therapeutic area programs in support of successful clinical studies Lead GCP audit strategy including audits of investigative sites, clinical vendors, internal department, TMF, and study documents Represent QA on clinical teams to provide compliance assessment and advice Manage clinical inspections by regulatory bodies across internal and ext

Director, GCP QA Compliance Our biotech partner is a well-established, commercially successful clinical stage biotech that is seeking a Director of Clinical Quality Assurance to lead the CQA function and build/manage a team. This role will oversee CQA strategy across policies, SOPs, deviations, change control, CAPAs, and vendor audits. This is a great opportunity for a Clinical QA leader to help progress a robust pipeline of therapeutics across oncology, neurology, endocrinology, and more areas. This position will be 3 days onsite in Redwood City, CA. Responsibilities: Lead Clinical Quality Assurance as a manager to the CQA team supporting various therapeutic area programs in support of successful clinical studies Lead GCP audit strategy including audits of investigative sites, clinical vendors, internal department, TMF, and study documents Represent QA on clinical teams to provide compliance assessment and advice Manage clinical inspections by regulatory bodies across internal and ext

Director, GCP QA Compliance Our biotech partner is a well-established, commercially successful clinical stage biotech that is seeking a Director of Clinical Quality Assurance to lead the CQA function and build/manage a team. This role will oversee CQA strategy across policies, SOPs, deviations, change control, CAPAs, and vendor audits. This is a great opportunity for a Clinical QA leader to help progress a robust pipeline of therapeutics across oncology, neurology, endocrinology, and more areas. This position will be 3 days onsite in Redwood City, CA. Responsibilities: Lead Clinical Quality Assurance as a manager to the CQA team supporting various therapeutic area programs in support of successful clinical studies Lead GCP audit strategy including audits of investigative sites, clinical vendors, internal department, TMF, and study documents Represent QA on clinical teams to provide compliance assessment and advice Manage clinical inspections by regulatory bodies across internal and ext

Director, GCP QA Compliance Our biotech partner is a well-established, commercially successful clinical stage biotech that is seeking a Director of Clinical Quality Assurance to lead the CQA function and build/manage a team. This role will oversee CQA strategy across policies, SOPs, deviations, change control, CAPAs, and vendor audits. This is a great opportunity for a Clinical QA leader to help progress a robust pipeline of therapeutics across oncology, neurology, endocrinology, and more areas. This position will be 3 days onsite in Redwood City, CA. Responsibilities: Lead Clinical Quality Assurance as a manager to the CQA team supporting various therapeutic area programs in support of successful clinical studies Lead GCP audit strategy including audits of investigative sites, clinical vendors, internal department, TMF, and study documents Represent QA on clinical teams to provide compliance assessment and advice Manage clinical inspections by regulatory bodies across internal and ext

Director, GCP QA Compliance Our biotech partner is a well-established, commercially successful clinical stage biotech that is seeking a Director of Clinical Quality Assurance to lead the CQA function and build/manage a team. This role will oversee CQA strategy across policies, SOPs, deviations, change control, CAPAs, and vendor audits. This is a great opportunity for a Clinical QA leader to help progress a robust pipeline of therapeutics across oncology, neurology, endocrinology, and more areas. This position will be 3 days onsite in Redwood City, CA. Responsibilities: Lead Clinical Quality Assurance as a manager to the CQA team supporting various therapeutic area programs in support of successful clinical studies Lead GCP audit strategy including audits of investigative sites, clinical vendors, internal department, TMF, and study documents Represent QA on clinical teams to provide compliance assessment and advice Manage clinical inspections by regulatory bodies across internal and ext

Overview We are seeking a Lead Designer to define and elevate the visual identity across educational and product-focused experiences in a hands-on, player/coach capacity. This hybrid role based in the San Francisco Bay Area will guide the creative vision while actively executing design work—especially during the early stages of team growth. The ideal candidate brings a blend of senior-level design expertise and leadership ability, with a passion for translating STEM concepts into fun, approachable visual content for students, educators, and families. Type: Direct hire, full time Schedule: regular business hours M-F Pay: $115,000 - $130,000 salary Lead Designer Duties Own and evolve the overall visual identity and design systems across all products, platforms, and brand materials Execute graphic design work for educational content, including student handouts, teacher guides, infographics, and interactive visuals Design engaging assets for web, print, packaging, and digital platforms, in

Job Description Job Description Position Overview: The EHS & Quality Manager provides leadership in safety, environmental, health, and quality management to ensure compliance with regulations and corporate standards. This role collaborates with plant leadership to implement and monitor EHS & Quality initiatives, fostering a culture of safety, compliance, and continuous improvement. Essential Responsibilities and Duties: Environmental, Health, and Safety (EHS): Implement and maintain Amcor’s EHS policies, ensuring compliance with regulations and corporate standards. Identify and assess workplace risks, developing appropriate preventive measures. Lead management of change processes and oversee contractor safety compliance. Review and analyze incident reports to determine trends and focus areas. Maintain knowledge of OSHA and EHS regulations, coordinating OSHA 300 log updates and submissions. Act as the primary liaison for external audits, including OSHA and environmental inspections. Con