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Mhra Jobs in California (NOW HIRING)

Overjet

Head of Regulatory

San Mateo, CA · On-site

$170K - $225K/yr

Serve as the primary point of contact with regulatory authorities (e.g., FDA, Health Canada, MHRA, TGA, EU Notified Bodies) for product approvals, QMS compliance, and ongoing reporting. * Interpret ...

Overjet

Head of Regulatory

San Mateo, CA · On-site

$210 - $260/hr

Serve as the primary point of contact with regulatory authorities (e.g., FDA, Health Canada, MHRA, TGA, EU Notified Bodies) for product approvals, QMS compliance, and ongoing reporting. * Interpret ...

MEDVACON

Medical Affairs Manager [515]

Foster City, CA · Hybrid

Provide guidance and oversight related to health authority (FDA, EMA, MHRA, etc.) regulations that impact the Medical Affairs organization. * May assist in development or review of Medical Affairs ...

MEDVACON

Medical Affairs Manager [515]

Foster City, CA · On-site +1

Provide guidance and oversight related to health authority (FDA, EMA, MHRA, etc.) regulations that impact the Medical Affairs organization. * May assist in development or review of Medical Affairs ...

micro1 AI

Regulatory Affairs Specialist

Berkeley, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Anaheim, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Modesto, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Richmond, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Pasadena, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Orange, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Regulatory Affairs Specialist

Lancaster, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Regulatory Affairs Specialist

Hayward, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Lancaster, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Regulatory Affairs Specialist

Clovis, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

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All JobsMhra JobsMhra Jobs in California

Mhra information

See California salary details

$15

$49

$74

How much do mhra jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for mhra in California is $49.79, according to ZipRecruiter salary data. Most workers in this role earn between $39.13 and $60.48 per hour, depending on experience, location, and employer.

What is an MHRA inspector?

MHRA inspectors are professionals employed by the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK. They are responsible for inspecting organizations that manufacture, distribute, or supply medicines and medical devices to ensure compliance with legal standards and regulations. Their work helps ensure that products are safe, effective, and of high quality for public use. MHRA inspectors also provide guidance, investigate complaints, and take enforcement action when necessary.

What kind of projects or responsibilities can a new MHRA inspector expect during their first year on the job?

As a new MHRA inspector, you can expect to be involved in a variety of projects focused on ensuring compliance with pharmaceutical regulations and safety standards. Early responsibilities often include conducting routine inspections of manufacturing sites, reviewing documentation for product approvals, and participating in team audits alongside more experienced inspectors. You'll also collaborate with regulatory affairs professionals, quality assurance teams, and sometimes external stakeholders. Comprehensive training and mentorship are provided to help you build expertise and gradually take on more complex cases. This role offers a strong foundation for career advancement within regulatory affairs or specialized inspection roles.

What are the key skills and qualifications needed to thrive as an MHRA regulatory affairs specialist, and why are they important?

To thrive as an MHRA regulatory affairs specialist, you need a strong understanding of pharmaceutical regulations, compliance processes, and often a life sciences degree. Familiarity with regulatory submission systems, document management tools, and knowledge of relevant certifications like RAC (Regulatory Affairs Certification) are typical requirements. Outstanding attention to detail, strong communication, and analytical thinking set top professionals apart in this field. These skills ensure accurate submissions, regulatory compliance, and effective collaboration with internal teams and external authorities, directly impacting public health and product success.

What is the difference between Mhra vs Pharmacist?

AspectMhraPharmacist
Required CredentialsRegulatory knowledge, compliance certificationsPharmacy degree, licensing, registration
Work EnvironmentRegulatory agencies, pharmaceutical companiesCommunity pharmacies, hospitals, clinics
Employer & Industry UsageHealth authorities, pharmaceutical industryHealthcare providers, retail pharmacies

While Mhra professionals focus on regulatory compliance and overseeing pharmaceutical standards, pharmacists are licensed healthcare providers who dispense medications and advise patients. Both roles are essential in the healthcare industry but serve different functions related to medication safety and regulation.

What are popular job titles related to Mhra jobs in California?

For Mhra jobs in California, the most frequently searched job titles are:

What job categories do people searching Mhra jobs in California look for?

The top searched job categories for Mhra jobs in California are:

Mhra jobs near you
Infographic showing various Mhra job openings in California as of August 2026, with employment types broken down into 40% Full Time, 58% Part Time, and 2% Contract. Highlights an 22% Physical, 1% Hybrid, and 77% Remote job distribution, with an average salary of $103,570 per year, or $49.8 per hour.

Regulatory Affairs Specialist

Qnovia, Inc.

Newport Beach, CA • On-site

$120 - $155/hr

Other

Medical, Dental, Vision, Retirement

Posted 4 days ago

Job description

Lead regulatory strategy and submission activities for Qnovia's drug-device combination products across FDA, MHRA, and other global regulatory bodies.

About the Role

Qnovia is advancing a portfolio of drug-device combination products through regulatory pathways in the United States and United Kingdom. As a Regulatory Affairs Specialist, you will develop and execute regulatory strategies, prepare submission documents, and serve as the primary liaison with regulatory agencies. This role requires deep knowledge of CDER and CDRH requirements for combination products.

Responsibilities
  • Develop and execute regulatory strategies for drug-device combination products
  • Prepare and manage IND, NDA, 505(b)(2), and MAA submissions
  • Author and review regulatory documents including briefing packages, meeting requests, and agency correspondence
  • Monitor and interpret evolving regulatory requirements and guidance documents
  • Support pre-submission meetings and formal interactions with FDA and MHRA
  • Collaborate with clinical, quality, and R&D teams to ensure regulatory compliance throughout product development
  • Maintain regulatory intelligence on combination product pathways and competitive landscape
  • Contribute to labeling development and promotional review activities
Qualifications
  • Bachelor's degree in life sciences, pharmacy, engineering, or related field; advanced degree preferred
  • 5+ years of regulatory affairs experience in the pharmaceutical or medical device industry
  • Direct experience with FDA CDER and/or CDRH submission processesKnowledge of 21 CFR Parts 210, 211, 314, 812, and 820
  • Experience with combination product regulatory pathways (21 CFR Part 3)
  • Strong technical writing and document management skills
Preferred Qualifications
  • Experience with inhaled drug products or respiratory drug delivery
  • Background in UK MHRA or EMA regulatory submissions
  • Experience with breakthrough therapy or fast-track designation processes
  • Familiarity with eCTD submission format and publishing tools

$120,000 - $155,000 annually, depending on experience. Equity participation included.

  • Comprehensive medical, dental, and vision insurance
  • Equity ownership in a pre-commercial stage company
  • Flexible hybrid work arrangement
  • 401(k) with company match

Qnovia, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by applicable federal, state, or local law.

If you require a reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please contact us at careers@qnovia.com.

This job description is intended to describe the general nature and level of work being performed by individuals assigned to this position. It is not intended to be an exhaustive list of all duties, responsibilities, and skills required. Qnovia reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

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