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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 ...

DGN Technologies

Senior QC Technician

Oceanside, CA · On-site

Eur, USP, ICH, MHRA, and related standards * Experience with LIMS systems (LabWare, CoreLims, LabVantage) * Experience with ELN/LES systems (especially ONELab from Biovia) * Experience with ...

Lancesoft INC

Senior QC Technician

Oceanside, CA · On-site

$30 - $36/hr

Eur, USP, ICH, MHRA, and related standards * Experience with LIMS systems (LabWare, CoreLims, LabVantage) * Experience with ELN/LES systems (especially ONELab from Biovia) * Experience with ...

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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 Aug 24, 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.

Head of Regulatory

San Mateo, CA • On-site

Overjet
Software Development • 11 - 50 employees
Learn more about Overjetexternal

$170K - $225K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago

Job description

Lead the Future of Dentistry.
Overjet is the world-leader in dental AI. Already, thousands of dental providers and insurers rely on our platform to deliver the best possible care. Now, we're looking for talented people to fulfill our mission: improve oral health for all.
Overjet is where builders become leaders. Everyone here loves to make new things: new products, new partnerships, new content, and a new category of AI technology. And as Overjet grows ridiculously fast, so will you.
Simply put, there's no better place to accelerate your career. Come join us!
The Role
Overjet is looking for a Head of Regulatory to own the critical regulatory function at a growing Healthtech AI company. As a key member of the Engineering team, reporting to our VP of Machine Learning & Compliance. This is an incredible opportunity to help lead the future of dental care - by building and leading the regulatory function as we scale.
Responsibilities
  • Develop, lead, and execute Overjet's global regulatory strategy, ensuring alignment with business goals and evolving international requirements.
  • Own the planning, coordination, and submission of regulatory filings, including FDA 510(k), De Novo, Health Canada Medical Device License (MDL), EU MDR (via SGS NB and Casus EU RP), UK MHRA registration (via Casus UK RP), and Australian TGA (via sponsor Emergo by UL).
  • 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 and communicate new or evolving global regulatory requirements across internal stakeholders, and incorporate them into Overjet's regulatory and quality systems.
  • Partner with Product, Clinical, Engineering, and QA teams to ensure regulatory requirements are embedded throughout the product lifecycle-including design controls, validation, verification, and risk management.
  • Manage development and maintenance of submission-ready documentation and regulatory dossiers.
  • Provide regulatory input for clinical studies, real-world evidence programs, and data usage strategies.
  • Collaborate with the VP of Machine Learning & Compliance and Director of Security to align regulatory strategies with privacy, cybersecurity, and AI risk management frameworks.
  • Support regulatory due diligence for partnerships, audits, and customer-facing compliance engagements.
  • Lead inspections and audits from regulatory authorities and Notified Bodies, and ensure timely resolution of findings.
  • Build and manage the regulatory team as Overjet scales globally.

Qualifications
  • 7+ years of experience in regulatory affairs for medical devices, including 2+ years with software as a medical device (SaMD) under FDA and at least one international regulatory framework (e.g., Health Canada, EU MDR, MHRA, TGA).
  • Proven success managing regulatory submissions and approvals in multiple jurisdictions (e.g., FDA 510(k), De Novo, CE Marking, MDEL, UK MHRA registration, TGA conformity assessments).
  • Deep knowledge of global regulatory frameworks including:
    • U.S. FDA (21 CFR Part 820, SaMD guidance)
    • Canada's Medical Devices Regulations
    • EU MDR and IVDR (including Notified Body processes)
    • UK Medical Device Regulations
    • Australian TGA (including sponsor model)
  • Experience interacting directly with agencies and notified bodies, including leading meetings and responses to questions or deficiencies.
  • Expertise in ISO 13485, ISO 14971, and IEC 62304; familiarity with ISO 27001 and data protection standards (HIPAA, GDPR) a plus.
  • Strong knowledge of quality management systems and compliance audits, including internal and external inspection readiness.
  • Excellent communication skills, including the ability to translate technical and regulatory language for cross-functional teams.
  • High degree of ownership, self-direction, and comfort working in fast-paced, high-growth environments.
  • Bachelor's degree in a scientific or engineering discipline required; advanced degree (e.g., MS, PhD, JD, MPH) or RAC credential preferred.

Why Overjet?
  • Competitive Compensation and Equity
  • Hybrid workplace that provides flexibility, vibrant in-person workspaces, and the ability to build strong connections across all of Overjet - regardless of location
  • 401k plans with a matching program
  • Medical, Dental and Vision coverage: 99% employee premium covered, 75% dependent premium covered
  • Life and AD+D Insurance
  • 8 weeks Paid Parental Leave
  • Optional HSA with Employer contribution
  • Flexible Time Off and company paid holidays
  • Annual Learning and Development Stipend

Our Hybrid Workplace
We have a unique hybrid workplace at Overjet - which combines the teamwork of meeting in person, with the flexibility of working from anywhere.
Many of our positions are based in San Mateo, New York City, Boston, and Salt Lake City. The Jetters who live in these "geo-hubs" come to the office on Tuesdays and Wednesdays, while having the option to work from home the rest of the week.
Our People Team is happy to answer any questions about what hybrid work means for your specific role!
Overjet's Values
  • Excellence: Aim Higher
  • Velocity: Quickly Deliver Results
  • Ownership: Go the Extra Mile
  • Win-win: Care Deeply

Company Recognition
  • Included on Best Places to Work by BuiltIn lists in 2026: #3 overall in the US, #1 in NYC, #1 in San Francisco, and #2 in Boston
  • #4 on FastCompanys's Most Innovative Companies list in Healthcare for 2026
  • Named one of the TIME Best Inventions of 2024
  • Recognized in Newsweek's Most Loved Workplaces in America 2024
  • Won the Dental Health category at the Digital Health Awards 2024 and 2024 Best Places to Work by Built In
  • Recognized as one of the Top Startups of 2023 by LinkedIn
  • Included on the definitive 2022 Forbes AI 50

EEOC
Overjet is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We believe diversity enriches our team so we hire people with a wide range of identities, backgrounds, and experiences. Even if you don't meet 100% of the qualifications for this job, we strongly encourage you to apply!
If you are a Colorado resident: Please contact us by emailing recruiting@overjet.ai to receive compensation and benefits information for this role. Please include the job title in the subject line of the email.

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