Top 20 Regulatory affairs Jobs in Oxnard Ca

QC Analyst III (Pharma)
Astrix Technology Group —Ventura, CA
- $58 - $60 an hour
- Contract
- 5 years
- Bachelor's degree
- Mentoring
Quick Apply
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
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
Senior Director, Oncology Pharmacology
Jazz Pharmaceuticals —California
- $232,000 - $348,000 a year
- Analysis skills
- Doctor of Philosophy
- Mentoring
- Health insurance
- Dental insurance
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
Senior Research Analyst
Truven Health Analytics, an IBM Company —Thousand Oaks, CA
- Microsoft Excel
- Master's degree
- Bachelor's degree
Quick Apply
QC Cell Culture Scientist (Biologist)
Avantor —Carpinteria, CA
- $69,000 - $110,975 a year
- Full-time
- Oracle
- Microsoft Outlook
- Bachelor of Science
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 Manager/Associate Director, Regulatory CMC Consultant (REMOTE)
Kaztronix —United States
- Contract
- Remote
- 6 years
- Management
- Bachelor's degree
Quick Apply
Vice President of Compliance
Scott & Associates, PC —United States
- Full-time
- Remote
- Data analysis skills
- HIPAA
- Finance
Deputy Chief Compliance Officer
Kaztronix —United States
- 11+ years
- Office
- Bachelor's degree
Quick Apply

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Sr Associate Regulatory Affairs - CMC
Amgen —Thousand Oaks, CA
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan. As we work to develop treatments that take care of…
$83,974.90 - $113,613.10 a year
6d
Sr Regulatory Affairs Associate, CMC
Kite Pharma —Santa Monica, CA
May act as Regulatory CMC representative on cross functional project teams by applying knowledge of regulations and interprets technical regulatory guidelines…
$115,260 - $149,160 a year

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Regulatory Affairs Manager - Labeling
Cardinal Health —Dublin, OH
Education: Bachelor’s degree in scientific, engineering, life sciences, or related field is preferred or equivalent work experience.
$105,100 - $150,100 a year
6d
Manager, Regulatory Affairs
Victoria's Secret —Reynoldsburg, OH
Experience improving processes, implementing tools, or driving operational efficiencies. Bachelor’s degree in a relevant field.
$112,700 - $153,720 a year

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QC Analyst III (Pharma)

Astrix Technology Group -
Ventura, CA

Quick Apply

Job Details

Contract
$58 - $60 an hour

Qualifications

Bachelor's degree
Pharmaceutical company experience
Chemical testing

Full Job Description

Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled QC Analyst III to join their team in Camarillo, CA!

Location: Ventura County, CA
Pay rate: $58 -$60/hr.
Job type: 6-month contract (possibility of extension or conversion)

Job Summary
The QC Analyst III is responsible for performing advanced analytical testing, data review, method validation, and laboratory investigations to support product quality and regulatory compliance. This role provides technical leadership for analytical activities, stability programs, and continuous improvement initiatives while collaborating with cross-functional teams to ensure timely and compliant laboratory operations.

Responsibilities

Perform complex analytical testing and data evaluation using techniques such as HPLC, ELISA, and other applicable methodologies.
Troubleshoot laboratory equipment and instrumentation issues, implement corrective actions, and communicate resolutions to management.
Participate in and support analytical method validations, verifications, and transfers.
Evaluate and trend analytical data to identify quality issues, process improvements, and potential risks.
Lead and support Out-of-Specification (OOS), Out-of-Trend (OOT), and atypical result investigations, including root cause analysis, product impact assessments, and implementation of CAPAs.
Collaborate with Quality Assurance, Manufacturing, Regulatory Affairs, and other departments to coordinate testing activities and communicate results.
Coordinate testing activities performed by external contract laboratories, including raw material, in-process, and finished product testing.
Maintain accurate, complete, and compliant laboratory records and documentation.
Author, execute, review, and approve SOPs, protocols, reports, investigations, change controls, risk assessments, and data summaries.
Develop, revise, and optimize analytical methods, testing procedures, and laboratory documentation.
Train laboratory personnel on analytical techniques, procedures, and compliance requirements.
Support laboratory equipment maintenance, qualification, calibration, and general upkeep activities.

Qualifications

Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Microbiology, or a related scientific discipline required; advanced degree preferred.
Minimum 5–8 years of experience in a pharmaceutical, biotechnology, or other regulated laboratory environment.
Demonstrated experience performing analytical testing using HPLC, ELISA, and other laboratory techniques.
Experience with analytical method validation, method transfer, and stability testing programs.
Strong understanding of cGMP regulations and applicable FDA, ICH, USP, and other regulatory requirements.
Experience conducting OOS/OOT investigations, root cause analysis, risk assessments, and CAPA implementation.
Proven ability to author and review technical documents, including SOPs, protocols, reports, and investigations.
Excellent organizational skills with the ability to manage multiple priorities and meet deadlines.
Strong verbal and written communication skills, including the ability to present technical information to diverse audiences.
Demonstrated leadership experience, including project management, mentoring, and training of laboratory personnel.
Proficiency with Microsoft Office applications and data analysis tools.
Ability to work independently and collaboratively within a cross-functional team environment.

Note: This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

INDBH
#LI-AH1

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Refine Your Search

regulatory affairs jobs in oxnard ca

QC Analyst III (Pharma)

Sr Associate Regulatory Affairs - CMC

Sr. Regulatory Affairs Specialist

Senior Director, Oncology Pharmacology

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)

Senior Research Analyst

QC Cell Culture Scientist (Biologist)

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 Manager/Associate Director, Regulatory CMC Consultant (REMOTE)

Vice President of Compliance

Deputy Chief Compliance Officer

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