Associate Director
$155k - $185kSutro Biopharma
Associate Director, EH&S and Facilities Sutro is seeking an Associate Director, EH&S and Facilities to lead EH&S compliance and equipment service management at our South San Francisco headquarters. Responsibilities Develop and partner with external consultants to lead the EH&S program, including safety training, job hazard assessments, periodic inspections, policy and SOP development, and appropriate documentation. Review, create, and continuously improve Sutro safety SOPs. Lead building-specific safety team meetings and drive actions to resolution. Review and audit waste handling procedures and coordinate with Facilities and scientific staff to assure compliance. Manage equipment service workflows for preventive maintenance, unplanned repairs, calibrations (e.g., pipettes, O2 monitors, scales), and cold storage defrosts. Create, schedule, track, and close service work orders in the CMMS; enter service reports and maintain equipment and calibration files. Coordinate new instrument and equipment setup, service readiness, vendor scheduling and escorting, and equipment decommissioning. Partner with lab users, Facilities, and service providers to communicate service status, verify completion, elevate safety or compliance issues, and support equipment-related on-call response. Qualifications A minimum of 5 years of EH&S experience, the majority of that time in the biopharmaceutical industry. Experience coordinating laboratory equipment service programs in a biopharmaceutical, laboratory, or regulated operations environment. Experience independently conducting health and safety inspections, training and program reviews and updates for a wide range of EH&S programs, including chemical, biological, radiological, general safety and life safety. Working knowledge of CMMS or Facilities work-order systems, equipment service documentation, and calibration or preventive maintenance tracking; experience with Faciliworks, Excel, Zendesk, D365, or similar tools is preferred. Knowledge of State and local health, safety, waste, and environmental regulations, procedures, and business practices, including a broad knowledge of health and safety best management practices. Excellent written and communication skills required for general correspondence, service coordination, report preparation, and documentation follow-through. Candidate must be highly motivated and excited to collaborate with various departments and relevant personnel, including Facilities, laboratories, administration, and service providers with minimal guidance. Excellent attention to detail and ability to track multiple equipment service activities through completion. Additional Qualifications Board certification in a related discipline (e.g., CIH, CSP, CHP, PE) is a plus, however not required. Experience supporting cold-storage assets or regulated lab equipment service programs is also desired. Sound exciting? Apply today and join our team! Sutro Biopharma, Inc. encourages all colleagues to be fully vaccinated for COVID-19 prior to the first date of employment. As an equal opportunity employer, we believe in fostering a culture that is inclusive and values diversity in background and opinions. Sutro Biopharma hires extraordinary individuals into every position in the company and is committed to the diversity of our team. Our company progresses without regard of race, ethnicity, gender, sexual orientation, religious belief, age, disability or citizenship status. We are dedicated to creating a safe environment where our employees can grow and succeed together. We look forward to hearing from candidates who are interested in exploring opportunities with Sutro! Our People & Culture team/hiring managers are unable to respond and do not accept solicitations from third-party agencies. The anticipated salary range for fully qualified candidates applying for this role at Sutro Biopharma’s California based locations will be $155,000 - $185,000 (not including bonus, equity, and benefits). The final salary offered will be dependent on several factors that include and are not limited to relevant previous experience, job responsibilities and duration of experience, the type and length of experience within the industry and education. About Sutro Biopharma Sutro Biopharma, Inc. is advancing a next-generation antibody‑drug conjugate (ADC) platform designed to deliver single‑and dual‑payload ADCs that enable meaningful breakthroughs for patients with cancer. By fully optimizing the antibody, linker, and payload, Sutro’s cell‑free platform produces ADCs that are engineered to improve drug exposure, reduce side effects, and expand the range of treatable tumor types. With unique capabilities in dual‑payload ADCs, Sutro aims to overcome treatment resistance and redefine what’s possible in cancer therapy. The Company’s pipeline of single‑and dual‑payload ADCs targets large oncology markets with limited treatment options and significant need for improved therapies. #J-18808-Ljbffr
$190k - $240k
...discoveries. These values are the foundation of our work, empowering us to make a real difference, every day. Position Title: Associate Director, Clinical Scientist Department: Clinical Development Reports To: VP, Clinical Development Lead (CDL) for each program Job...SuggestedFull timeFlexible hours$141k - $194k
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Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles...Local area- Pharmacological And Toxicological Assessment This individual will participate in the pharmacological and toxicological assessment at Company by developing and implementing nonclinical strategies, including creating a best-evidence synthesis of existing knowledge and...Work at office
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## Associate Director, Clinical Supply PlanningApplyremote type: Hybridlocations: South San Francisco, Californiatime type: Full timeposted on: Posted Yesterdayjob requisition id: R543Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its...Worldwide$250k - $270k
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...high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Position Summary This role will report to the Sr. Director Program Management. It is the execution engine of the late‑stage clinical program, managing overall project timelines, risks, and...Work experience placementOverseasAfternoon shift2 days per week1 day per week- About the job Associate Director Medical Writing Role Overview We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation. This individual will play a key role in shaping document strategy...Contract workWork at office
$155k - $193.2k
...Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director will be responsible for the oversight of Translational Science preclinical safety assessment/toxicology deliverables, with a...Work at officeLocal areaRemote workNight shift3 days per week$186k - $235k
...chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Position Summary The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company...Remote work$230k - $240k
...create an inspiring and exciting place to catalyze and enable medical breakthroughs. Position Description Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high...For contractorsWork at office$200.7k - $234.15k
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...Overview Placement Type: Temporary Salary: $60-74 Hourly Start Date: Aug 3, 2026 Associate Creative Director Reports To: Creative Director Location: Remote (Ideally San Francisco or Los Angeles) Work Environment: Hybrid (3 days/week...Hourly payTemporary workWork at officeRemote work3 days per week$210k - $240k
...assist with regulatory filings. This position reports to Senior Director, CMC Program Management and is responsible for the following:... ...Additional Information The anticipated salary range for Associate Director level candidates who will work on-site at our South San...H1b$137.5k - $261k
...priorities across the organization. The work of this team plays a vital role in shaping AbbVie's continued growth and success. The Associate Director of AI Transformation will support major change initiatives and drive organizational transformation to enable AbbVie’s...Temporary work$182.07k - $235.62k
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$150k - $174k
...clients and internal innovation, using technology to unlock insights from data at unprecedented scale and speed. The role Our Associate Directors are experienced communications leaders who combine real advisory authority with a genuine appetite to keep developing –...Work at office$186k - $233k
...Revolution Medicines in San Francisco seeks an Associate Director of Business Operations to manage internal projects within the Development & Clinical Sciences organization. The candidate will design and implement business capabilities to support vital growth in a collaborative...- ...Razorfish is seeking an Associate Director of Program Management to lead operational efforts for CRM and email marketing initiatives. You will bridge Customer Engagement, Business Strategy, Technology, Big Data, and Content, guiding small-to-medium engagements across...
$188k - $190k
Responsibilities Lead the Cost Management team on specific client commissions, making sure that the team delivers on all accountabilities. Interface with clients, stakeholders, and consultants across all project stages to ensure alignment on scope, budget, and deliverables...Full timeContract workFor contractors$219k - $256k
...Director, Global Drug Substance Commercialization, Critical Raw Materials Join to apply for the Director, Global Drug Substance Commercialization... ...supply of critical raw materials for production of eCRM and associated components for glycoconjugate vaccines. This role focuses on...RelocationRelocation package
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