Director, Drug Substance
$211k - $264kRevolution Medicines
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS‑addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC‑6236), a RAS(ON) multi‑selective inhibitor; elironrasib (RMC‑6291), a RAS(ON) G12C‑selective inhibitor; zoldonrasib (RMC‑9805), a RAS(ON) G12D‑selective inhibitor; and RMC‑5127, a RAS(ON) G12V‑selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity Playing a critical role as a technical lead within the Drug Substance function, the position will be responsible for process research and development and scale‑up of manufacturing in support of Revolution Medicines’ pipeline compound development, clinical programs and commercial readiness. Responsibilities Responsible for developing chemical processes for the manufacture of drug substance, intermediates and/or starting materials, including route evaluation and process optimization. Conduct process development and optimization studies according to the principles of quality by design (QbD), to enable regulatory starting materials designation, establish control strategy and process characterization studies using tools such as design of experiment (DOE) studies. Lead and/or enable technology transfer, process familiarization, and manufacturing at CDMOs. Participate in identification, selection, and management of CROs and CDMOs including management of redundant supply and geographic diversity. Write, review, and approve protocols, manufacturing batch records, and development and campaign reports. Author, review the relevant CMC sections of regulatory filings and patent applications. Partner with analytical development, pharmaceutical development, and supply chain functions to design overall strategy for programs. Communicate effectively within cross functional project teams. Travel to CRO/CDMO for the oversight of development activities and manufacturing (up to approximately 15%). Required Skills, Experience and Education PhD (minimum MSc degree) in organic chemistry, chemical engineering or related discipline. 10 or more years (15+ years for Master’s degree) of relevant industrial experience in chemical / drug substance process research and development. Strong people management skills. Hands‑on proficiency in synthetic organic chemistry. Knowledge of current ICH guidelines, GMP, and relevant industry practices. Working experience and knowledge of regulatory submissions (IND, IMPD, NDA and MAA). Previous experience managing projects at CROs/CDMOs. Strong problem solving skills with sound technically driven decision‑making ability. Effective written and verbal communication skills and interpersonal skills. An innovative team‑player with high energy for our dynamic company environment. The base pay salary range for this full‑time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job‑related skills, experience, market dynamics, and relevant education or training. Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities. Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status. Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact View email address on click.appcast.io. Base Pay Salary Range
$211,000 - $264,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message. Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address. If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to View email address on click.appcast.io so we can share these impersonations with our IT team for tracking and awareness. #J-18808-Ljbffr Revolution Medicines$175k - $210k
...a team committed to transforming medicine in autoimmune diseases, starting with the kidney. Position Summary:TheAssociate Director, Drug Substance Manufacturing - Downstream Process will report to the VP, Commercial Manufacturing Operations and will be responsible all...SuggestedContract workFor contractorsFlexible hours$211k - $264k
Revolution Medicines, located in Redwood City, CA, is seeking a Technical Lead for Drug Substance. The position involves leading chemical process development and optimization for drug manufacturing. Ideal candidates will possess a PhD or MSc, with over 10 years in the...Suggested$193k - $246k
...a pivotal inflection point.insitro is seeking an (Associate) Director, Drug Product Operations to lead drug product strategy and execution... ...across the CMC value chain — equally comfortable in drug substance, analytical, and supply chain discussions as in formulation and...SuggestedWork at officeLocal areaRemote workHome officeFlexible hours3 days per week- Septerna, a biotechnology company in South San Francisco, is seeking an Associate Director of Process Chemistry to lead drug substance development across our small molecule programs. This role will act as an SME and guide strategic CMC direction, collaborating with CDMOs...Suggested
- BBOT, a clinical-stage biopharmaceutical company, seeks an Associate Director of Drug Product Development to lead formulation and process development for small molecules from preclinical through commercial stages. You will oversee solid oral dosage forms, manage external...Suggested
$188.5k - $219k
All Jobs > Associate Director, Drug Product, CMC BBOT is a clinical-stage biopharmaceutical company advancing a next-generation pipeline of novel small molecule therapeutics targeting RAS and PI3K malignancies. BBOT has the goal of improving outcomes for patients with...Flexible hours$160k - $180k
...your career, and for what’s beyond.About the Role >>> Associate Director GMP QualityAs the Associate Director, GMP Quality, reporting... ...role will be oversight of the manufacture of small molecule drug substances (Active Pharmaceutical Ingredients). There will be associated...Work experience placementWork at officeFlexible hours$164k - $205k
...pathway. Revolution Medicines is seeking an experienced and strategic leader to serve as Senior Manager, Commercial Manufacturing, Drug Substance within the PDM organization. This individual will play a critical role in advancing/supporting the company’s API commercial...Full timeLocal area- Revolution Medicines is seeking a Senior Manager, Commercial Manufacturing, Drug Substance to provide technical leadership across late-stage drug substance development, tech transfer, CPV, lifecycle management, and capacity planning for our API portfolio. You will oversee...
$243.41k - $256.8k
...Inc. has job openings (multiple) for the position of Associate Director, Chemical Development based out of its location in Brisbane,... ...: Responsible for regulatory starting materials (RSMs) and Drug Substance (DS) cGMP manufacturing related activities, including scale-up...Contract work$200k - $220k
...leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company’s Native Complex Platform... ...an experienced and highly motivated Associate Director of Process Chemistry to manage and drive drug substance process development and delivery activities across...Full timeContract work- Septerna seeks an Associate Director of Process Chemistry to lead drug substance development across small molecule programs in South San Francisco, CA. You will drive route evaluation, optimization, scale-up, and GMP production while coordinating with CDMOs and cross-functional...
- Our client is looking for a seasoned Associate Director/Director, Fill Finish and Packaging. The biopharma client is located in the... ...manufacturing to interface with RA, QA, QC, FAC, VAL, PD, SC, and drug substance production teams. Direct the work of fill-finish...Contract work
$225k - $270k
POSITION SUMMARY: The Drug Safety Physician in Drug Safety & Pharmacovigilance department will serve as a subject matter expert and thought leader for drug safety activities across Rigels portfolio. This role requires broad expertise in oncology drug development, precision...Flexible hours- Nurix Therapeutics, Inc. in Brisbane, CA is hiring an Associate Director, Chemical Development to lead cGMP manufacturing of drug substance and to manage CMOs for scale‑up and process validation. The role supports regulatory submissions and quality compliance across programs...
$68.64k - $120.02k
...background check, occupational health clearance, vaccines and immunizations, and drug testing for certain positions. Drug testing may include screening for marijuana which remains an illegal substance according to federal law. The failure to pass required drug testing will...Full timeWork experience placementLocal area$33 - $48.68 per hour
...background check, occupational health clearance, vaccines and immunizations, and drug testing for certain positions. Drug testing may include screening for marijuana which remains an illegal substance according to federal law. The failure to pass required drug testing will...Hourly payFor contractorsWork at office$186k - $233k
...in the RAS signaling pathway. The Opportunity The Associate Director, GMP Quality Assurance will provide quality oversight and decision... ..., testing, and batch disposition of small molecule Drug Substance (DS) and Drug Product Intermediate (DPI). The role ensures GMP...Full timeContract workWork at officeLocal area$160k - $195k
...A biotechnology company in South San Francisco seeks a qualified professional to design synthetic strategies and develop drug candidates. Candidates must have a PhD in Chemistry and at least 5 years of experience. The role involves collaboration within multidisciplinary...Full time- insitro is seeking an Associate Director, Drug Product Operations to lead DP strategy and execution for our early‑stage pipeline, spanning pre‑clinical through first‑in‑human studies. You will own formulation, DP process development, fill/finish, and CDMO partnerships...Remote job
$188k - $215k
...Sr. Manager/Associate Director, CMC Regulatory SciencesSan Francisco - 1800 Owens Mavericks WantedWhen was the last time you achieved... ...Solutions. This position will work with CMC technical teams (Drug Substance, Drug Product, and Analytical Development) and Regulatory...Full timeWork at officeLocal areaRemote workFlexible hours$130k - $150k
...Range: $130,000.00 To $150,000.00 Annually The TBNC Site Director is responsible for day-to-day management and... ...genders identities, sexual orientations, people who use substances, including injection drugs, those experiencing homelessness, people with mental health...Work experience placementSeasonal workAll shiftsNight shiftAfternoon shift$290k - $365k
...condition, you are a person with a disability. Disabilities include, but are not limited to: Alcohol or other substance use disorder (not currently using drugs illegally) Autoimmune disorder, for example, lupus, fibromyalgia, rheumatoid arthritis, HIV/AIDS Blind or low...Contract workFor contractorsFor subcontractorWork at officeVisa sponsorshipFlexible hours$365k
...operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985. Alcohol or other substance use disorder (not currently using drugs illegally) Autoimmune disorder, for example, lupus, fibromyalgia, rheumatoid arthritis, HIV/AIDS Blind or...Visa sponsorship- ...Job Description Job Description Job: Associate Director/Principal Scientist, CMC Analytical Chemistry Location: San Francisco... ...activities and oversee the testing and release of drug substance and drug product at contract manufacturers/service providers...Full timeContract workWork at office
$210k - $250k
POSITION SUMMARY: The Director, Drug Safety & Pharmacovigilance (DSPV) Operations, serves as a senior operational leader and subject matter expert for safety activities across Rigels portfolio. The Director is accountable for the strategy, execution, governance, and continuous...Contract workWork experience placementLocal areaRemote workFlexible hours$10k
About the Role:We are seeking a highly motivated and accomplished Associate Director with deep expertise in immunology and drug discovery to join the Immunobiology Open Innovation Team within the Immunology Research Unit. This role is based in our South San Francisco West...Full timeTemporary workLocal areaRelocation$110k - $165k
...expectations and be responsive when critical issues arise is key to your success in this role and our collective success as a team.A Drug Free Workplace: Clark promotes a drug free workplace. A pre-employment drug “fitness for duty” screening is required, and the...Full timeTemporary workWork at office- Director/Senior Director Drug Product Development and Manufacturing Department/Group: CMC Location: South San Francisco, CA Position Type: Full... ...Analytical Development functions to define optimal drug substance properties and control strategies Ensure adherence to applicable...Full timeImmediate start
- Position Summary Serve as a subject matter expert and thought leader for drug safety activities across the portfolio, applying oncology drug development, precision medicine biomarkers, and global regulatory frameworks. Responsibilities Perform comprehensive medical review...Flexible hours
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