Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard of care and improving outcomes for patients living with breast cancer and beyond. It’s an exciting time to be part of Team Olema, with
Job Summary We are seeking an experienced Business Systems Analyst (BSA) that supports regulatory compliance, patient safety, and continuous product improvement through accurate and timely documentation, assessment, investigation, reporting, and resolution of customer complaints. This role
Senior Manager, Life Sciences Supply Chain & Operate Lead the evolution of Deloittes AI-enabled Business Process Outsourcing (BPO) capability for Life Sciences clients. This Senior Manager role sits at the intersection of client delivery, operating model
Associate Director, GMP Quality San Francisco or Boston office with 10-15% travel, some international Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard of care and improving outcomes for patients living with breast
GxP Project Manager We are seeking an experienced GxP Project Manager to lead and manage cross-functional GxP initiatives supporting pharmaceutical manufacturing, quality, laboratory, validation, and IT systems. The ideal candidate will have strong experience delivering GxP-compliant
Job Description We are seeking an experienced Principal Quality Engineer to provide technical leadership in quality engineering, regulatory compliance, and continuous improvement initiatives. This role is responsible for driving quality strategy across the product lifecycle, supporting
Associate Director, Regulatory CMC San Carlos, California, United States Join Our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have
Sr. Manager, Regulatory Affairs Join our mission to protect humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work ScheduleStandard (Mon-Fri) Environmental
Job Description We are seeking an experienced Principal Quality Engineer to provide technical leadership in quality engineering, regulatory compliance, and continuous improvement initiatives. This role is responsible for driving quality strategy across the product lifecycle, supporting
Quality Systems Specialist The resource should have 2-3 years of prior experience in a regulated cGMP environment. Prior experience in the pharmaceutical/biotech sector is preferred. The resource should have a combination of experience in the Quality
QA Documentation Specialist-I Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in