Top 23 Regulatory affairs Jobs in Oxnard Ca

Sr Associate Regulatory Affairs - CMC
Amgen —Thousand Oaks, CA
- $83,974.90 - $113,613.10 a year
- Remote
- Bachelor of Science
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
6d
Senior Director, Oncology Pharmacology
Jazz Pharmaceuticals —California
- $232,000 - $348,000 a year
- Analysis skills
- Doctor of Philosophy
- Mentoring
- Health insurance
- Dental insurance
Sr. Regulatory Affairs Specialist
Caldera Medical —Westlake Village, CA
- $100,000 - $130,000 a year
- Full-time
- Microsoft Excel
- 5 years
- Office
- Paid parental leave
- AD&D insurance
Quick Apply
Regulatory Expert, Digital Pathology
Agilent Technologies Inc —Carpinteria, CA
- $124,160 - $232,800 a year
- Full-time
- Engineering
- 8 years
- In-person
- Work from home
Executive Director of Regulatory Affairs - Obesity and Related Conditions
Amgen —Thousand Oaks, CA
- $255,301.75 - $345,408.25 a year
- 6 years
- Doctoral degree
- Writing skills
- Disability insurance
- Health insurance
Executive Director, Global Medical Affairs, GU, GI & Hematology Platform
Amgen —Thousand Oaks, CA
- $325,301.80 - $440,114.20 a year
- Remote
- Medicine
- 6 years
- Bachelor's degree
- Disability insurance
- Health insurance
Director, Global Regulatory Lead – Obesity & Related Conditions (Chronic Weight)
Amgen —Thousand Oaks, CA
- $195,640.25 - $264,689.75 a year
- Doctoral degree
- Office
- Master's degree
- Disability insurance
- Health insurance
QC Cell Culture Scientist (Biologist)
Avantor —Carpinteria, CA
- $69,000 - $110,975 a year
- Full-time
- Oracle
- Microsoft Outlook
- Bachelor of Science
Senior Research Analyst
Truven Health Analytics, an IBM Company —Thousand Oaks, CA
- Microsoft Excel
- Master's degree
- Bachelor's degree
Quick Apply
Associate Director, Medical Writer
MannKind Corporation —Westlake Village, CA
- $148,000 - $222,000 a year
- 7 years
- Bachelor of Science
- Bachelor's degree
Quick Apply
Executive Director, Medical Director- Diabetes
MannKind Corporation —Westlake Village, CA
- $224,000 - $336,000 a year
- Medicine
- Doctor of Philosophy
- Travel
Quick Apply
Director, Regulatory Affairs – CMC
Rocket Pharmaceuticals —United States
- $204,000 - $264,000 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
【Up to $190K plus bonus】 Medical Science Liaison (Rare Disease) |South, Southeast, and Midwest
Leverages U.S. Inc. (Shigotosagashi.com) —United States
- $16,000 - $190,000 a year
- Full-time
- Remote
- Spanish
- Medicine
- Up to 50% travel
- Health insurance
- Dental insurance
Quick Apply
10d
Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island
Vertex Pharmaceuticals —United States
- $171,300 - $256,900 a year
- Full-time
- English
- Mentoring
- Data entry
- Loan repayment program
- Health insurance

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Sr Associate Regulatory Affairs - CMC

Amgen -
Thousand Oaks, CA

Apply Now

Job Details

$83,974.90 - $113,613.10 a year
6 days ago

Benefits

Disability insurance
Health insurance
Dental insurance
Flexible spending account
Vision insurance
Retirement plan

Qualifications

Project reporting
Biotechnology
Document control experience within pharmaceutical industry
Bachelor of Science
Drug regulation
Project timeline management
Master's degree
High school diploma or GED
Records management
Pharmaceutical company experience
Quality control
Compliance documentation
Project delivery management
Organizational skills
Chemistry, manufacturing & controls
Regulatory submission editing and review
Managing projects
Quality assurance experience within manufacturing
Manufacturing
Senior level
Training
Cross-functional collaboration
Associate's degree
Leadership
Communication skills
Cross-functional communication
Product lifecycle management

Full Job Description

United States - Remote

JOB ID: R-248904 LOCATION: United States - Remote ; US - California - Thousand Oaks WORK LOCATION TYPE: Remote DATE POSTED: Jun. 29, 2026 CATEGORY: Compliance SALARY RANGE: 83,974.90USD -113,613.10 USD

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

SENIOR ASSOCIATE REGULATORY AFFAIRS – CMC

What you will do

Let’s do this. Let’s change the world. In this vital role you will facilitate product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle.

Amgen is searching for a Senior Associate to join the Regulatory Optimization of Technical, Surveillance, and Strategic Support (ROOTS2) group within RA CMC. The ROOTS2 team supports CMC submission execution for Amgen products across phases of development, modality, and country. The RA CMC Senior Associate will interface with the Amgen global, international, site and biosimilars RA CMC teams as well as the device team for specific strategies or activities that impact a product. The RA CMC Senior Associate will be responsible for varying levels of product support, including leading projects, based upon their experience level.

Responsibilities:

Contribute as a member of the global regulatory CMC product team
Interact with authors/reviewers and subject matter experts with respect to delivery of regulatory documents required for regulatory submissions
Contribute to the organization and preparation of CMC investigational product amendments, post‑market supplements/variations, and new marketing applications
Document and archive CMC submissions and related communications in the document management system
Initiate and maintain CMC product timelines at the direction of product lead
Interface with the regulatory operations team
Train staff on select CMC procedures and systems
Provide report status of activities and projects to teams and department
Participate in cross-functional special project teams

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The detail-oriented professional we seek is a collaborative and proactive team player with these qualifications.

Basic Qualifications:

Master’s degree

Bachelor’s degree and 2 years of Pharmaceutical/Biotech and/or Healthcare and/or Med Device and/or Scientific experience

Associate’s degree and 6 years of Pharmaceutical/Biotech and/or Healthcare and/or Med Device and/or Scientific experience

High school diploma / GED and 8 years of Pharmaceutical/Biotech and/or Healthcare and/or Med Device and/or Scientific experience

Preferred Qualifications:

BS degree in life science
Experience in manufacture, process development, quality assurance, quality control, or analytical development
Regulatory CMC specific knowledge and experience
Developed project management and organizational skills
Strong and effective oral and written communication skills

What you can expect from us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

and make a lasting impact with the Amgen team.

careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

Apply Now

Refine Your Search

regulatory affairs jobs in oxnard ca

Sr Associate Regulatory Affairs - CMC

Senior Director, Oncology Pharmacology

Sr. Regulatory Affairs Specialist

Regulatory Expert, Digital Pathology

Executive Director of Regulatory Affairs - Obesity and Related Conditions

Executive Director, Global Medical Affairs, GU, GI & Hematology Platform

Director, Global Regulatory Lead – Obesity & Related Conditions (Chronic Weight)

QC Cell Culture Scientist (Biologist)

Senior Research Analyst

Associate Director, Medical Writer

Executive Director, Medical Director- Diabetes

Director, Regulatory Affairs – CMC

【Up to $190K plus bonus】 Medical Science Liaison (Rare Disease) |South, Southeast, and Midwest

Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island