91 regulatory associate jobs at 54 companies in Camp Pendleton North, CA
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Senior Regulatory Affairs Associate
Lake Forest, California, United States
$103k-$133k/yrOnsiteFull Time
AlconNYSE: ALC: Manufactures ophthalmic surgical equipment and vision care products.
2+ YOEBachelor's degree or equivalent experience, 2 years relevant experience, 1 year leadership, knowledge of regulatory submissions, GxP/SOP adherence, strong English communication, onsite in Lake Forest, CA.
Associate Director / Director, Regulatory Affairs - CMC
San Diego, California, United States
$164k-$245k/yrHybridFull Time
Iambic Therapeutics: Develops novel medicines using an AI-driven discovery platform.
8+ YOEBachelor's degree in a relevant scientific discipline, 8+ years' experience for Associate Director or 10+ for Director, substantial CMC regulatory experience, Module 3 content expertise, and global regulatory knowledge.
Travere TherapeuticsNASDAQ: TVTX: Developing and selling therapies for rare kidney diseases.
8+ YOEBachelor's degree in a scientific discipline and 8+ years of biotechnology or pharmaceutical regulatory experience, including significant CMC expertise in biologics development, submissions, and lifecycle management.
IND, IMPD, CTA, BLA, NDA, MAA, Module 2, Module 3, FDA, EMA, MHRA, PMDA, ICH
Rapport TherapeuticsNASDAQ: RAPP: Developing precision medicines for neurological and psychiatric disorders.
10+ YOEBachelor's in life science, 10+ years pharma/biotech experience, global drug development and neurology/small-molecule experience preferred, experience with FDA neurology divisions, leadership, strong communication.
AbbVieNYSE: ABBV: Develops and sells innovative pharmaceutical and biopharmaceutical medicines.
8+ YOEBachelor's degree in science and 8 years of relevant industry experience required; PharmD and 6 years preferred. Requires advertising and promotion regulatory expertise, matrix-environment experience, and strong communication skills.
Ensign ServicesNASDAQ: ENSG: Provides administrative and clinical support to post-acute healthcare facilities.
0+ YOEJuris Doctor degree, 0–3 years of legal practice, and admission in good standing to at least one state bar. Requires strong research, analytical, writing, communication, and matter-management skills.
Clinical Research Regulatory Coordinator: Hoag Clinical Research
Newport Beach, California, United States
$39-$61/hrOnsiteFull Time
Hoag: Operates hospitals and healthcare centers in Orange County, California.
1+ YOEAssociate degree or equivalent required; bachelor's preferred. Requires over one year of clinical research regulatory documentation experience. FDA, NIH, OHRP, and ICH GCP knowledge preferred.
Applied Medical: Manufacturer of advanced medical devices and surgical products.
Bachelor's degree in Engineering or sciences; regulatory labeling experience; strong writing and project management; cross-functional collaboration; familiarity with QSRs, GMPs, ISO standards.
Senior Clinical Research Associate (level dependent on experience)
San Diego, California, United States
RemoteFull Time
CTI Clinical Trial and Consulting Services: Global CRO providing clinical research services.
2+ YOEBachelor or Master in allied health or RN with associate degree/nursing diploma; 2+ years clinical nursing; site monitoring and regulatory knowledge.
PIMCO: Global investment management firm specializing in fixed income strategies.
3+ YOEBachelor’s degree required; J.D. strongly preferred. Minimum 3–5 years legal/compliance experience in financial services; experience with client contracting, regulatory filings, and U.S. securities laws. Microsoft Excel proficiency.
Catalent: Global provider of drug development and manufacturing solutions.
Bachelor’s degree in physical, chemical, biological, or pharmaceutical science required; formulation and analytical techniques, accurate records, SOP and regulatory compliance, and Microsoft Office experience preferred.
Dairy Farmers of America: Produces and distributes milk, cheese, butter, and dairy ingredients.
0+ YOEUndergraduate degree or equivalent,0–2 years transportation/dispatch/supply chain experience, knowledge of distribution/regulatory requirements, Microsoft Office and TMS preferred, must be able to communicate in English.
Microsoft Office Suite, Transportation Management Systems (TMS)
PCI Pharma Services: Integrated pharmaceutical development, manufacturing, and global packaging services.
6+ YOEBachelor's degree in life sciences or equivalent experience, 6+ years of relevant QA experience, and GMP manufacturing experience preferred. Requires regulatory knowledge, QMS software experience, collaboration, auditing, and training skills.
Schwan's Company: Manufactures and distributes frozen pizzas and desserts.
0+ YOEHigh school diploma or GED preferred; 0–1 year related sanitation or food manufacturing experience preferred. Requires knowledge of cleaning, safety, regulatory, and GMP procedures.
Walgreens: Retail pharmacy providing prescriptions and health and wellness products.
Provides courteous, efficient checkout and customer service, handles transactions, maintains merchandising and store appearance, follows asset-protection and regulatory procedures, and completes assigned training.
Environment, Energy & Resources - Associate Attorney – Midlevel
Washington or Palo Alto or Anchorage or San Francisco or New York or Chicago or San Diego or Portland or Phoenix or Madison or Boise or Bellevue or Seattle
$190k-$390k/yrHybridFull Time
Perkins Coie: International law firm providing legal and business counsel.
3+ YOE3-6 years energy law experience; regulatory and transactional background; draft energy contracts; FPA familiarity; JD; bar admission or eligibility to waive.
IQVIANYSE: IQV: Provides clinical research and healthcare data analytics services.
Perform site monitoring and management per protocol and regulations, support recruitment and documentation, evaluate site quality, and manage regulatory submissions and TMF/ISF documentation.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, iPhone, iPad
IQVIANYSE: IQV: Provides clinical research and data analytics for pharmaceutical companies.
Bachelor's degree in science or healthcare preferred, or equivalent education and experience; clinical research regulatory knowledge, CRA training or monitoring experience, computer proficiency, English communication, and organizational skills.
Good Clinical Practice (GCP), International Conference on Harmonization (ICH), Microsoft Word, Microsoft Excel, Microsoft PowerPoint, iPhone, iPad, Trial Master File (TMF), Investigator's Site File (ISF)
8+ YOEPhD in a relevant biological field and 8+ years of biopharma experience in biomarker development, clinical biomarker strategy, and operations; assay validation, CRO transfer, regulatory documents, and staff management required.