Associate Director, GMP Quality San Francisco, California Apply 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 our transformation into a fully integrated oncology company well underway, top-line data from our lead program expected later this year, and our first potential commercial launch on the horizon. Our lead product candidate, palazestrant, is a novel, orally available complete estrogen receptor antagonist (CERAN) and selective estrogen receptor degrader (SERD) currently in two pivotal Phase 3 clinical trials. We expect top-line data from OPERA-01, our ongoing Phase 3 trial of palazestrant as a monotherapy in patients with second- or third-line ER+/HER2- metastatic breast cancer (MBC), in the fall which, if successful, could lead to our first potential approval and commercial launch in 2027. OPERA-02, our Phase 3 trial of palazestrant in combination with ribociblib in patients with frontline ER+/HER2- MBC, is enrolling patients. Together with its mechanism of action, pharmacokinetic properties, and the potential to demonstrate activity in both ESR1 wild-type and mutant tumors, palazestrant has the potential to transform the metastatic breast cancer treatment paradigm and access a $15 billion global market opportunity. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with the potential to generate further value and meaningfully impact the metastatic breast cancer treatment landscape – particularly in combination with palazestrant. We recently reported encouraging Phase 1 monotherapy data from this program across multiple solid tumor types and are advancing patient enrollment in the ongoing combination arms in MBC. Aspiring to transform the metastatic treatment paradigm is an ambitious endeavor that requires a resolute approach to developing better therapies and a passionate team dedicated to helping the patients we serve feel better, longer. We possess a deep commitment to our shared purpose, the sustained pursuit of excellence, cultivating the courage required to advance our programs, drive to succeed, and a collective capacity for adaptability through learning, growth, and evolution. Team Olema is made up of nimble self-starters who bring consistency in their quest for the extraordinary every single day. If you’re ready to be part of a tenacious, courageous, agile, and growing team, join us in making a profound impact, together – for our patients, for your career, and for what’s beyond. About the Role >>> Associate Director GMP Quality As the Associate Director, GMP Quality, reporting to the Head of GMP Quality, you will be responsible for oversight of GMP activities pertaining to Olema’s products, both clinical and commercial. The focus of this role will be oversight of the manufacture of small molecule drug substances (Active Pharmaceutical Ingredients). There will be associated responsibilities for reviewing Analytical Development / Quality Control results. In this position you will perform GMP activities such as, but not limited to, review of Certificate of Analysis, Batch Disposition, Person in Plant oversight, and supporting Supplier compliance. In this role you will also collaborate with other functional teams such CMC, Regulatory and Supply Chain to prepare submissions, ensure quality and compliance for Olema’s products. This role will be based out of our San Francisco or Boston office and will require 10-15% travel, some international. Your work will primarily encompass: Batch disposition/ release for Clinical Trial Materials and Commercial batches Perform technical review, quality oversight and approvals Master Batch records and Executed Batch records Review and approval of CMO Deviations, CAPA, and Change Controls and opening of internal shadow records when required Perform technical review of Quality Control records such as Certificate of Analysis, Analytical Testing, Method Validation and Stability reports Operational oversight of Olema’s CMOs as specified in quality agreements; this may include periodic visits to CMOs Represent Olema as Person in Plant (PIP) when critical processing occurs as necessary Support Pre-Approval Inspection readiness for NDA / commercial launch Review sections of New Drug Applications for content and accuracy Review Quality Agreements and support Supplier audits as necessary Interact with Qualified Persons (QP) to facilitate the release of Clinical and Commercial product Generate metrics for Quality Management Reviews Contribute and participate in Annual Product Quality Reviews of commercial products Represent GMP Quality during internal and regulatory inspections Author Quality department SOPs as required Ideal Candidate Profile >>> Key Requirements A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role. Knowledge: Bachelor’s degree is required; advanced degree (MS, PharmD, PhD) preferred Extensive understanding and knowledge of industry standards, concepts and current cGMP (21 CFR Parts 210 and 211), EudraLex Volume 4, ICH Q7 and other agency standards and guidance as they relate to GMP Quality Assurance Experience: Minimum of 8 years' work experience in an FDA regulated Pharmaceutical GMP / GMP QA role Experience with small molecule synthesis and analytical test record review Prior experience with NDA/BLA submission and commercial launch for pharmaceutical products Familiarity with effective Quality Systems and performing robust investigations Experience with Health Authority filings and EU QP queries Experience managing CMO relationships and supporting CMO inspections Experience with Quality Management Systems such as Veeva or TrackWise Proficient in Word, Excel, PowerPoint, SharePoint Attributes: Demonstrated proven track record of leadership, communication, adaptability, and collaboration Communicate decisions and recommendations with clear background and justification A strong team player with the ability to focus on project objectives with an emphasis on quality Clear, concise writing skills and good verbal presentation skills Ability to prioritize, work independently, and mindfully engage with others The base pay range for this position is expected to be $160,000 - $180,000 annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits. Important Information >>> We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated. We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants. Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you. Fraud Alert: We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview. Apply for this job * indicates a required field First Name* Last Name* Preferred First Name Email* Phone Country* Phone* Location (City)* Locate me Resume/CV* Attach Attach Dropbox Google Drive Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Cover Letter Attach Attach Dropbox Google Drive Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Home Address* City* State* Zip Code* LinkedIn Profile* Website Are you legally authorized to work in the United States?* Select... Do you now or will you in the future require employer sponsorship?* Select... Submit application Powered by

Listed by Olema Oncology for a position based in the United States. Employers on this board attest they are hiring domestically.

Biotech/Pharma

57 days ago

Principal Analytical QA Specialist, Drug Substance

Loyal · Remote - US

Pay

$150k–190k

Setting

Remote

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Back to jobs Principal Analytical QA Specialist, Drug Substance Remote - US Apply About Loyal Loyal is a clinical-stage veterinary medicine company developing longevity drugs for dogs. Our mission is to help dogs live longer, healthier lives. We're pioneering a new category of veterinary prescription drugs that proactively and preventatively target the underlying drivers of aging, delaying the onset of disease and preserving quality of life as dogs age. We've already made significant progress in our mission to develop the first FDA-approved drugs to extend canine lifespan: as of early 2026 we've completed two of three major FDA review sections for our lead program, LOY-002, and are targeting submission of the third and final section later this year. Loyal is a well-funded startup with teams of scientists, veterinarians, engineers, operators, and creatives. You'll help us continue on our path of earning FDA approval for the first lifespan extension medicine for any species, and change what's possible for the dogs we love. About the role We’re seeking an experienced Principal Analytical QA Specialist, Drug Substance to provide Quality Assurance oversight of GMP manufacturing, release, stability, validation, and lifecycle management activities supporting the development and commercialization of Loyal's veterinary pharmaceutical products. Operating within Loyal's fully outsourced manufacturing network, the position supports batch disposition of active pharmaceutical ingredient (API) / drug substance, drug product, packaging and labeling through review and approval of protocols, reports, analytical methods, and associated GMP documentation. The role works collaboratively with Technical Operations and Analytical Development / Quality Control to ensure that the manufacture and laboratory analysis of drug substance, drug product, packaging & labeling of finished drug product conforms with cGMPs, VICH and global regulatory requirements. This position also partners with CMC Regulatory Affairs to ensure the translational accuracy and integrity of data incorporated into Module 3 sections of CTD regulatory submissions and written responses to regulatory authorities. Your daily work will include Manufacturing & Analytical Quality Oversight Oversee all aspects of drug manufacture and testing through clinical development and into commercial phase. Provide Quality oversight for analytical method development, qualification, validation, transfer, release testing, and stability programs supporting drug substance and drug product development. Support establishment of phase-appropriate specifications, stability-indicating methods, and control strategies aligned with regulatory expectations. Review and approve validation protocols, raw data, and reports (for test method, process, cleaning, etc.). Batch Release / Disposition & Quality Systems Manage the batch release program by reviewing executed documentation, raw data, quality events (change controls, deviations, CAPAs, OOS/OOT investigations, risk assessments) and product disposition decisions. Review and approve master and executed batch records, analytical raw data, stability protocols, reports and data, and other documents to enable drug substance and final drug product release and on-going evaluation ensuring batches are compliant with cGMP requirements. Lead or support quality event resolution investigations (e.g., OOS/OOT results, deviations), ensuring root cause analysis, CAPA development, and timely closure. Support inspection readiness, audit programs, risk management, quality metrics reporting, Annual Product Review (APR) and product quality processes, Field Alert Report (FAR), product withdrawal, and product recall process. Regulatory & Cross-Functional Support Perform data integrity and compliance assessments including review against source documentation for regulatory submissions. Maintain effective communication with Contract Development and Manufacturing Organizations (CDMOs) and Contract Testing Laboratories (CTLs) to ensure Quality objectives are achieved in accordance with project timelines. Maintain awareness of evolving veterinary pharmaceutical regulations and ensure compliance strategies are updated accordingly About you B.S./M.S. degree in in a scientific discipline (Pharmaceutical Sciences, Chemistry, Veterinary Science, or related field) Minimum 12 years of relevant pharmaceutical industry experience, with at least 6 years in GxP QA roles. Strong knowledge of FDA CVM regulations, cGMP, and VICH guidelines applicable to veterinary products In-depth working knowledge of drug substance development and manufacturing, analytical method development, validation, release testing, stability programs, and quality systems. Experience managing CDMOs and collaborating effectively across cross-functional teams. Capable of working successfully in a team/matrix environment and independently, as required. Ability to meet deadlines, demonstrate efficient and effective use of time, and handle multiple assignments simultaneously. Ability to convey both written and verbal information effectively and efficiently. Demonstrated ability to follow procedures and perform assignments with a high degree of accuracy and careful attention to detail. Willingness to travel (10%). Core Competencies: Strong technical judgment and problem-solving Attention to detail and commitment to quality Excellent written and verbal communication Ability to influence cross-functional teams and external partners Effective project and time management Collaborative mindset with a continuous improvement focus Preferred Qualifications: Other Compliance or Regulatory certifications (e.g., RAC, ASQ) a plus. Experience auditing suppliers, CDMOs, and CTLs. Experience with Google Workspace applications (e.g., Sheets, Slides, etc.) and electronic Quality Management Systems. Experience in small molecule pharmaceutical development, routine analytical testing for solid oral dosage forms, and/or veterinary drug products preferred. Experience with international regulatory environments (EU, Canada, etc.) a plus Salary Range: $150,000 - $190,000 Loyal benefits Full-coverage health insurance — medical, dental and vision — for you and your dependents $1,000 home office equipment stipend $1,200/year learning budget for books, courses, etc. $250/month wellness budget for gym, cleaners, spa, food, etc. All 3-day weekends are turned into 4-day weekends 🎉 Unlimited vacation and paid holidays Paw-ternity leave — adopt a dog and get a day off with your new family member 🐶 Competitive salary Company equity options grant for new hires Loyal is founded and led by a first-gen female CEO and is proud to be an equal opportunity employer. We do not discriminate against applicants based on gender, race or color, ethnicity or national origin, age, disability, religion, sexual orientation, gender identity or expression, veteran status, or any other applicable characteristics protected by law. Our values Moonshots, derisked methodically Bringing the first longevity drug to market is an extremely difficult technical and social pursuit. To achieve this we must take bigger bets than the field has historically made, paired with the technical rigor to de-risk them step by step. We plan on both short and extremely long timescales, and we have the conviction to see our vision through to success or failure. Opportunity is at the intersection We lean into combining disciplines, expertise, and perspectives not normally adjacent. We design our organization to facilitate cross-pollination and cross-collaboration. We reject silos. Expertise without ego Titles do not determine who has a voice. We push back on each other, ask questions instead of issuing orders, and try to prove ourselves wrong. We are emotionally attached to the outcome, not our personal hypotheses, and welcome being challenged instead of treating it as a threat. High agency, high humility Most of what we're doing has never been done before, so we can't rely on established precedents to guide our way. We move forward to generate clarity, build strategies resilient to the fact that we don't know what we don't know, and design small experiments where we can fail safely, without jeopardizing the bigger mission. Lead with transparency and context We proactively and consistently share the why behind our strategy - not just the what - because we believe sharing context enables great people to make great decisions. Empathy and respect for all life Our patients are not just numbers. We deeply respect the value of every life, large and small and take our ethical responsibility to the families we treat extremely seriously. Create a Job Alert Interested in building your career at Loyal? Get future opportunities sent straight to your email. Create alert Apply for this job * indicates a required field Autofill my application First Name* Last Name* Email* Phone Country* Phone* Location (City)* Locate me Resume/CV* Attach Attach Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Cover Letter Attach Attach Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Do you now or in the future require sponsorship for employment?* Select... LinkedIn Profile Website Submit application Powered by

Listed by Loyal for a position based in the United States. Employers on this board attest they are hiring domestically.

Biotech/Pharma

58 days ago

Cell Therapy Specialist II (26101-B-683-MFG)

ArsenalBio · San Francisco (UCSF)

Pay

$85k–104k

Setting

On-site

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WHO WE ARE

ArsenalBio, a privately held, clinical-stage programmable cell therapy company engineering advanced CAR T therapies for solid tumors, is seeking a talented Cell Therapy Specialist II to work onsite based in our Hayward/UCSF and San Francisco office.

ArsenalBio’s mission and purpose is very clear: defeat cancer. With our programmable and computationally driven approach, our team is engineering medicines with the goal to attack cancer’s inherent multifaceted nature and overcome the challenges of addressing solid tumors with cell therapy.

Driven by a collective of diverse experts across multi-scientific disciplines as well as clinical and manufacturing expertise, we are united in our purpose to develop the optimal medicines for improving patients’ lives.

This means you’ll have the opportunity to work with the best talent in the field of cell therapy, and be part of ONE TEAM advancing therapies for patients who need it most.

ArsenalBio is seeking a talented and motivated Cell Therapy Specialist to join the ArsenalBio Technical Operations team supporting cell therapy manufacturing activities. This Specialist will work closely with Manufacturing, Process Development, Quality and other support roles. The position will report into the Director of Manufacturing in supporting day to day manufacturing processes. The individual will also interact cross-functionally across the organization to enable the success of ArsenalBio. This position requires a Tuesday to Saturday schedule and may require on-call off hours beyond that to support business needs.

Listed by ArsenalBio for a position based in the United States. Employers on this board attest they are hiring domestically.

Biotech/Pharma

59 days ago

Research Associate I, Platform Reagents & Assay Support

BigHat Biosciences · San Mateo, CA, US

Pay

$75k–88k

Setting

On-site

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Research Associate I, Platform Reagents & Assay Support

Department: Lab Science

Employment Type: Full Time

Location: San Mateo, CA

Description

The role: BigHat Biosciences is seeking a self-motivated individual for a Research Associate I, Platform Reagents & Assay Support (PRAS), role to power our in-house reagent manufacturing and QC efforts supporting our Milliner platform.

Key Responsibilities

Execute automated and manual high-throughput reagent manufacturing and QC workflows to support data generation across BigHat’s production assay suite.
Keep detailed records of all reagent lot manufacturing and QC events using BigHat’s documentation tools, and clearly communicate results and challenges.
Contribute to reagent lot performance monitoring, and assist with troubleshooting efforts as needed.
Collaborate on the creation of laboratory standard operating procedures (SOPs) for reagent manufacturing and QC.
Collaborate closely with BigHat team members to identify, design, and implement critical process and operational improvements to workflows and laboratory systems.
Operate automated liquid handlers and analytical instruments to ensure all lab and platform operations run efficiently.

Skills Knowledge and Expertise

BS in Biology or Chemistry, with 1+ year(s) of industry experience.
Experience in reagent manufacturing and quality control, process execution, and troubleshooting.
Hands-on experience with, or interest in, automated liquid handlers (e.g. Hamilton, OpenTrons, Tecan, Agilent systems). Experience with LIMS is a nice-to-have.
Experience with molecular biology techniques and general lab practices.
Efficient time management and ability to work on several projects simultaneously, in a dynamic start-up environment.
Strong interpersonal skills and ability to effectively communicate with members of a multidisciplinary team.
Excellent record keeping abilities to document experimental work and analytical data.
Nice-to-haves include previous experience working with barcoding systems and automated tube/plate labelers, inventory tracking, and experience with Google Workspace tools (Docs, Sheets, Slides, etc.)

Total Rewards

The salary estimated for this position is $75,000 - $88,000 + bonus + options + benefits. Compensation will vary depending on job-related knowledge, skills, and experience. Actual compensation will be confirmed in writing at the time of the offer.

What BigHat Offers:

Range of health insurance plan options through Anthem and Kaiser (monthly credit if benefit waived)
Dental, and vision coverage through Guardian
Additional well-being benefits through Nayya, OneMedical, Wagmo, Rula, and more
401(k) with company match
DTO, two weeks of company-wide shutdown, and 12 company holidays
Paid parental leave

Listed by BigHat Biosciences for a position based in the United States. Employers on this board attest they are hiring domestically.

Biotech/Pharma

64 days ago

Chemist

Neuralink · Austin, Texas, United States

Pay

$71k–119k

Setting

On-site

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Back to jobs Chemist Austin, Texas, United States Apply About Neuralink: We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world. Team Description: The Biocompatibility Team is responsible for executing a wide range of assays, performing method validations, finalizing reports, and supporting R&D activities. We are a dedicated group of highly skilled professionals committed to ensuring the accuracy, reliability, and regulatory compliance of test methods used in quality control. With deep expertise in analytical techniques, including chemical characterization, microbiological testing, and biocompatibility evaluations, as well as manufacturing processes such as cleaning, sterilization, and passivation, this team plays a critical role in maintaining the highest standards of product quality and patient safety. Job Description and Responsibilities: The Chemist will collaborate with cross-functional teams across Neuralink to analyze the chemical and biological characteristics of manufacturing processes and finished devices. This role involves various levels of product testing during R&D and product release to generate data required for regulatory approvals. The data produced will help confirm patient safety in accordance with applicable global regulations, regulatory guidelines, and voluntary consensus standards. Daily responsibilities include drafting internal procedures and test protocols, sample preparation, laboratory testing, method development, inventory management, and other general laboratory tasks. The primary goal of the Chemist is to support medical device chemical and biological characterization to ensure patient safety and facilitate regulatory approval. Additional responsibilities include: Preparing test samples and controls for analysis Performing chromatographic and mass spectrometric analysis using instruments such as LC-MS, GC-MS, and ICP-MS Conducting routine and non-routine testing of materials and products to ensure compliance with quality standards and regulatory requirements, including performing calibration checks and maintaining proper documentation Delivering test results related to device characteristics to support manufacturing changes and risk assessments Preparing laboratory reports that comply with applicable medical device evaluation standards and FDA/ISO guidance documents within a risk-based framework Collaborating with cross-functional teams to support multiple projects, ensuring timely completion of laboratory deliverables to meet project timelines Analyzing test results to determine whether data meets internal and external requirements; utilizing problem-solving skills and technical expertise to troubleshoot unexpected outcomes Participating in continuous improvement initiatives to increase laboratory efficiency, reduce turnaround times, and enhance data quality Required Qualifications: Bachelor of Science in Chemistry, Biochemistry, or a related field 1-2 years of experience in an analytical laboratory Strong knowledge of basic laboratory operations, including weighing, sample handling, and preparation of volumetric solutions Ability to perform routine analytical chemistry calculations (for example, dilutions, concentrations, and result calculations) Basic understanding of laboratory safety and proper use of engineering controls (for example, fume hoods and biological safety cabinets) Demonstrated ability to develop and optimize analytical methods for efficiency and compliance Strong problem-solving mindset Excellent written and oral communication skills Preferred Qualifications: Master’s degree in Chemistry, Biochemistry, or a related field Familiarity with Good Laboratory Practices (GLP) and/or Good Manufacturing Practices (GMP) Hands-on experience with LC-MS, GC-MS, and ICP-MS Familiarity with chromatography data systems Experience with statistical analysis Experience troubleshooting analytical instrumentation Experience performing bioanalytical procedures and cell-based assays Experience with method validation and transfer Expected Compensation: The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees. Base Salary Range: $71,000 - $119,000 USD What We Offer: Full-time employees are eligible for the following benefits listed below. An opportunity to change the world and work with some of the smartest and most talented experts from different fields Growth potential; we rapidly advance team members who have an outsized impact Excellent medical, dental, and vision insurance through a PPO plan Paid holidays Commuter benefits Meals provided Equity (RSUs) *Temporary Employees & Interns excluded 401(k) plan *Interns initially excluded until they work 1,000 hours Parental leave *Temporary Employees & Interns excluded Flexible time off *Temporary Employees & Interns excluded Get new jobs like this in your inbox We'll email you when Neuralink posts a job like this one. Create alert Apply for this job * indicates a required field Autofill my application First Name* Last Name* Email* Phone Country* Phone* Resume/CV* Attach Attach Dropbox Google Drive Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Cover Letter Attach Attach Dropbox Google Drive Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Please provide three examples of accomplishments that highlight your exceptional ability. Provide quantitative details and metrics to describe your impact. First example:* Second example:* Third example:* Are you currently authorized to work in the United States?* Select... Will you, at any point, require employer sponsorship to work in the United States?* Select... I am willing and able to work entirely on-site.* Select... I will need relocation to work on-site.* Select... Ideal start date in office* How did you hear about us?* Select... Please specify LinkedIn Profile Additional Link Include a link to any additional content (e.g. personal website, Github, portfolio, etc.) Preferred Pronouns Submit application Powered by

Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.

Biotech/Pharma

64 days ago

Environmental Health and Safety Specialist

Neuralink · Fremont, California, United States

Pay

$63k–114k

Setting

On-site

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Back to jobs Environmental Health and Safety Specialist Austin, Texas, United States; South San Francisco, California, United States Apply About Neuralink: We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world. Team Description: At Neuralink, safety isn't a checkpoint, it's what lets us move fast without breaking the people who build the future. The Safety Team is the tactical extension of our engineers and scientists, embedding directly into high-stakes labs and facilities to eliminate hazards before they slow anyone down. We own the programs that protect our people, visitors, and contractors, and we run them at the pace the mission demands. We're looking for a high-speed, high-ownership individual who runs toward problems, thrives in ambiguity, and wants their work to directly enable Neuralink's mission of building a brain interface that restores autonomy and unlock human potential. Job Description and Responsibilities: As an Environmental Health and Safety Specialist / Engineer at Neuralink, you will support and help drive the day-to-day functions of the Safety Team across our two California locations — South San Francisco and Fremont — as well as other functions throughout the company. This is a role for a highly motivated person who has deliberately chosen EHS as their career, or an experienced technical lead ready to own and manage multiple EHS programs across both sites. You will continuously maintain facility permits and registrations to comply with local, state, and federal regulations while improving existing safety programs, training, processes, and operations. We are looking for a well-rounded, mechanically-inclined team member who takes ownership, works independently across sites, and enjoys unique projects that push them outside their comfort zone. You will regularly split your time between the South San Francisco and Fremont facilities and be trusted to prioritize and advance programs at both. Additionally, you will be expected to: Manage and coordinate EHS programs across both the South San Francisco and Fremont sites, adapting priorities to each location's needs Support regulatory compliance across both the South San Francisco and Fremont sites — maintaining facility permits, registrations, and reporting obligations with local, state, and federal agencies (e.g., CUPA, air district, RCRA, DTSC), and coordinate/lead inspections and audits Manage the day-to-day hazardous waste lifecycle at both sites — identification, labeling, accumulation, storage, manifesting, and disposal Administer stormwater, industrial wastewater, SPCC, and soil management programs, and prepare the associated discharge and compliance reports on schedule Track changing environmental and safety regulations across two sites and, with guidance and oversight from the EHS Lead, translate new requirements into site-specific programs and corrective actions Collaborate with engineers and scientists to ensure their processes are safe, and review new and existing chemicals Required Qualifications: 3+ years of experience within a health and safety role 3+ years of experience handling, storing, safekeeping, and removing hazardous materials (e.g., acids, bases, solvents) Strong knowledge of local, state, and federal regulatory agencies and requirements (e.g., stormwater, hazardous waste, industrial wastewater, spill prevention, control, countermeasure (SPCC), and soil management) Excellent written and verbal communication skills Preferred Qualifications: EHS Certifications such as ASP: Associate Safety Professional, CSP: Certified Safety Professional, and CIH: Certified Industrial Hygienist Bachelor’s Degree in Environmental Engineering, Environmental Science, or Environmental-related discipline or equivalent industry experience Prior experience in building facilities (e.g., HVAC, DI water, CDA, Nitrogen, Vacuum, exhaust) and wastewater treatment (AWN) Previous experience preparing hazardous waste, stormwater, and wastewater discharge reports Familiarity with setting up EHS programs and training such as LOTO, Hazard Communication, Emergency Response, Fall Protection, Respiratory Protection, Hearing Conservation, Equipment Safety, Lockout/Tagout, Ergonomics, etc. Technical background knowledge of chemical interactions and handling Prior experience analyzing, developing, and implementing corrective actions to ensure safe working environments Knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices) Additional Requirements and Competencies: Must be able to lift up to 50 lbs Ability to stand and walk for 10+ hours daily Ability to climb stairs Expected Compensation: The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees. Base Salary Range: $63,000 - $114,400 USD What We Offer: Full-time employees are eligible for the following benefits listed below. An opportunity to change the world and work with some of the smartest and most talented experts from different fields Growth potential; we rapidly advance team members who have an outsized impact Excellent medical, dental, and vision insurance through a PPO plan Paid holidays Commuter benefits Meals provided Equity (RSUs) *Temporary Employees & Interns excluded 401(k) plan *Interns initially excluded until they work 1,000 hours Parental leave *Temporary Employees & Interns excluded Flexible time off *Temporary Employees & Interns excluded Create a Job Alert Interested in building your career at Neuralink? Get future opportunities sent straight to your email. Create alert Apply for this job * indicates a required field Autofill my application First Name* Last Name* Email* Phone Country* Phone* Resume/CV* Attach Attach Dropbox Google Drive Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Cover Letter Attach Attach Dropbox Google Drive Enter manually Enter manually Accepted file types: pdf, doc, docx, txt, rtf Please provide three examples of accomplishments that highlight your exceptional ability. Provide quantitative details and metrics to describe your impact. First example:* Second example:* Third example:* Are you currently authorized to work in the United States?* Select... Will you, at any point, require employer sponsorship to work in the United States?* Select... I am willing and able to work entirely on-site.* Select... I will need relocation to work on-site.* Select... Ideal start date in office* How did you hear about us?* Select... Please specify LinkedIn Profile Additional Link Include a link to any additional content (e.g. personal website, Github, portfolio, etc.) Preferred Pronouns Which onsite location would you like to apply to?* Select... Submit application Powered by

Listed by Neuralink for a position based in the United States. Employers on this board attest they are hiring domestically.

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