Top 202 Director of regulatory affairs Jobs in Fremont, Ca

Director, CMC QC Small Molecules
Ultragenyx Pharmaceutical —South San Francisco, CA
- $232,600 - $287,400 a year
- Hybrid work
- 5 years
- Master's degree
- Bachelor's degree
- Gym membership
Consumer Affairs Supervisor
National Beverage Corp. —Hayward, CA
- From $74,000 a year
- Full-time
- Marketing
- Ability to walk for extended periods
- 5 years
- Health savings account
- Health insurance
Quick Apply
5d
Director, Regulatory Affairs
Nova Pneuma, Inc. a wholly owned subsidiary of Lee's Pharmaceuticals Holdings —Fremont, CA
- From $230,000 a year
- Office
- Analysis skills
- Bachelor's degree
Quick Apply
Associate Director, Regulatory Affairs (on-site)
Abbott Laboratories —Alameda, CA
- $148,700 - $297,300 a year
- Full-time
- Computer science
- Computer Science
- 5 years
- Health insurance
- Tuition reimbursement
Director, Quality & Regulatory Affairs
Abbott Laboratories —Livermore, CA
- $172,000 - $344,000 a year
- Full-time
- 5 years
- Analysis skills
- Bachelor's degree
- Health insurance
- Tuition reimbursement
Assoc Regulatory Affairs Strategy Director (Oncology)
Exelixis, Inc. —Alameda, CA
- $195,000 - $277,500 a year
- Email
- 5 years
- Writing skills
- Office
- Paid holidays
- Disability insurance
Senior Director, Regulatory Affairs (Oncology)
Exelixis, Inc. —Alameda, CA
- $248,000 - $352,500 a year
- Email
- 11+ years
- Office
- Master's degree
- Paid holidays
- Disability insurance
Director of Regulatory Affairs
Epia Neuro —Alameda, CA
- $198,000 - $248,000 a year
- Full-time
- Office
- Neurology
- Senior level
- Paid parental leave
- Health insurance
Quick Apply
Associate Director, Regulatory Affairs (Onsite in S.SF - 3X/wk)
Zai Lab (US) LLC —South San Francisco, CA
- $198,000 - $257,000 a year
- Full-time
- Hybrid work
- Office
- Bachelor's degree
- Doctor of Philosophy
- Paid time off
- Parental leave
Quick Apply
Sr Manager/Assoc Director, CMC Regulatory Affairs
Erasca —South San Francisco, CA
- $175,000 - $205,000 a year
- Remote
- 5 years
- Bachelor's degree
- Quality control
- Health savings account
- AD&D insurance
Director - Quality Management & Regulatory Affairs
Stanford Health Care —Palo Alto, CA
- $89.01 - $117.94 an hour
- Full-time
- Microsoft Excel
- Master's degree
- Travel
DIRECTOR OF DEVELOPMENT AND EXTERNAL AFFAIRS
Axis Community Health —Pleasanton, CA
- $145,000 - $155,000 a year
- Full-time
- Clean driving record
- Marketing
- Public speaking
- 403(b) matching
- Paid holidays
Director, Regulatory Affairs CMC - Cell Therapy & Novel Therapeutics
Retro —Redwood City, CA
- $225,000 - $260,000 a year
- Full-time
- 7 years
- Office
- Bachelor's degree
- Paid parental leave
- Paid holidays
Quick Apply
Senior Director, Regulatory Affairs Advertising & Promotion
Summit Therapeutics —Palo Alto, CA
- $217,000 - $271,000 a year
- 11+ years
- Bachelor's degree
- Travel
Quick Apply
12d
Senior Manager / Associate Director, Regulatory Affairs
Neurona Therapeutics —South San Francisco, CA
- $150,000 - $195,000 a year
- Doctor of Philosophy
- Team management
- Mentoring
Quick Apply
10d
Senior Director, Head of Regulatory Affairs
Orca Bio —Menlo Park, CA
- $250,000 - $300,000 a year
- Full-time
- Bachelor's degree
- Continuous improvement
- Organizational skills
- Disability insurance
- Health insurance
Senior Director, Regulatory Affairs
Summit Therapeutics —Palo Alto, CA
- $203,000 - $253,000 a year
- Remote
- Doctoral degree
- 5 years
- Master's degree
Quick Apply
9h
Director, Regulatory Affairs CMC, Combination Products and Device
Gilead Sciences —Foster City, CA
- $210,375 - $272,250 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
- Health insurance
- Dental insurance
6d
Director of Regulatory Affairs and Policy
SupplyBank.org —Oakland, CA
- $115,000 - $130,000 a year
- Full-time
- Hybrid work
- Office
- Master's degree
- Bachelor's degree
- Dental insurance
- Vision insurance
Quick Apply
Director, Regulatory Affairs
CALICO —South San Francisco, CA
- $275,000 - $280,000 a year
- Full-time
- Office
- Master's degree
- Doctor of Philosophy

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Director, CMC QC Small Molecules

Ultragenyx Pharmaceutical -
South San Francisco, CA

Apply Now

Job Details

$232,600 - $287,400 a year

Benefits

Gym membership

Qualifications

Dissolution testing
USP standards
Drug regulation
ICH guidelines
Laboratory regulatory affairs
Pharmaceutical company experience
Pharmaceutical analysis
Chemistry, manufacturing & controls
Communication with regulatory authorities for clinical trials
Quality control experience within pharmaceutical industry
Pharmaceutical manufacturing facility experience
Mass spectrometry

Full Job Description

Why Join Us?

Be a hero for our rare disease patients

At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won't go – challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life-changing treatments. We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in ways that are most meaningful for them.

Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth – so employees can thrive in all areas of their lives, in and outside of work. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work.

If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team.

Position Summary:

ultradedicated – Your biggest challenges yield rare possibilities

The Director, CMC Quality Control – Small Molecules is responsible for providing technical and strategic oversight of all outsourced QC activities supporting Ultragenyx small molecule drug substance and drug product programs across development and commercialization. This position reports to the Executive Director, CMC‑QC. The role leads QC governance for contract manufacturing organizations (CMOs), contract laboratories (CLs), and other external partners, ensuring compliant, phase‑appropriate, and inspection‑ready execution. QC testing experience supporting rare and ultra‑rare disease development models—characterized by lean organizations, accelerated timelines, and high reliance on outsourced partners—is a strong asset. Experience with biologics QC is considered an additional advantage, particularly for candidates supporting hybrid portfolios in a virtual QC model.

Work Model:

Flex: This role will typically require onsite work 2-3 days each week, or more depending on business needs. In many locations, the business will set certain days each week that Flex employees are required to be onsite.

Responsibilities:

Provide end‑to‑end QC oversight for a 100% outsourced operating model, supporting small molecule drug substance and drug product programs across clinical and commercial stages.
Provide technical and strategic leadership for small molecule QC, including solid oral dosage forms and sterile parenterals, with hands‑on oversight of analytical testing, method validation, investigations (deviations, OOS), CAPAs, and lifecycle management in compliance with ICH/USP/Ph. Eur./JP requirements.
Perform technical review and approval of outsourced analytical data, method validation, stability programs, reference standards, specifications, and shelf‑life assignments, ensuring phase‑appropriate QC strategies and data integrity.
Lead the selection, qualification, and performance management of CMOs and contract laboratories, serving as the QC technical representative during manufacturing campaigns and managing quality agreements, scopes of work, and issue resolution.
Collaborate cross‑functionally and lead CMC QC contributions to regulatory submissions, inspections, and audits, including authoring and defending QC sections and managing responses to health authority observations.
Oligonucleotide Biologics QC (Advantage) - Provide QC oversight or strategic input for biologics and/or oligonucleotide programs, including analytical methods, stability, and regulatory interactions, as needed.
Lead selection, qualification, onboarding, and ongoing performance management of contract laboratories and QC service providers, including governance models, KPIs, and issue escalation.
Act as the QC representative in cross‑functional CMC teams, collaborating closely with Technical Operations, Analytical Development, QA, Regulatory Affairs, Supply Chain, and Program Management.
Lead QC support for regulatory inspections and audits involving CMOs and CLs; author and manage responses to QC‑related observations and commitments.

Requirements:

Bachelor's degree with 14+ years or Master's degree with 10–12+ years, or PhD with 8–10+ years of relevant GMP experience in chemistry, pharmaceutical sciences, biochemistry, or a related discipline.
Minimum 5–8+ years of direct CMC QC experience supporting small molecule drug substance and drug product, including commercial assets.
Demonstrated hands‑on expertise with small molecule analytical techniques, including HPLC/UPLC, LC‑MS, GC, dissolution, Karl Fischer, particle size, residual solvents, impurity profiling, and compendial safety testing.
Strong working knowledge of ICH, FDA, EMA, USP, and Ph. Eur. requirements applicable to small molecule development and commercialization.
Proven experience overseeing external QC laboratories, CMOs, and contract testing organizations, including technical governance and performance management.
Experience supporting global regulatory submissions and health authority inspections, including defense of outsourced QC data.
Quality control experience working within rare and/or ultra‑rare disease development models, including lean organizations, accelerated timelines, and high reliance on outsourced partners, is a strong asset.
Experience applying digital, automation, and/or AI‑enabled solutions within QC or CMC environments, such as analytical data review, trend analysis, stability modeling, data integrity monitoring, or outsourced partner performance management, is a strong asset.

#LI-CS1 #LI-Hybrid

Full Time employees across the globe enjoy a range of benefits, including, but not limited to:

Generous vacation time and public holidays observed by the company

Volunteer days

Long term incentive and Employee stock purchase plans or equivalent offerings

Employee wellbeing benefits

Fitness reimbursement

Tuition sponsoring

Professional development plans

Benefits vary by region and country

Ultragenyx Pharmaceutical 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 and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at [email protected].

See our CCPA Employee and Applicant Privacy Notice.

See our Privacy Policy.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Note to External Recruiters: All candidate activity and open positions are managed strictly through our Human Resources Department. Our Human Resources Department kindly requests that recruiters not contact employees/hiring managers directly in an attempt to solicit business and present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organization. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation. Inquiries on developing a recruiting relationship with us, may be directed to: [email protected].

Apply Now

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director of regulatory affairs jobs in fremont, ca

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