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Mhra Jobs (NOW HIRING)

micro1 AI

Compliance Officers

Port Saint Lucie, FL · Remote

$50 - $70/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

Palm Bay, FL · Remote

$50 - $70/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

Detroit, MI · Remote

$50 - $70/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

Tulsa, OK · Remote

$50 - $70/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

Garland, TX · Remote

$50 - $70/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

Mckinney, TX · Remote

$50 - $70/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

Columbia, SC · Remote

$50 - $70/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

Rockford, IL · Remote

$50 - $70/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

Gilbert, AZ · Remote

$50 - $70/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

Palm Bay, FL · Remote

$50 - $70/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

Davenport, IA · Remote

$50 - $70/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

New Braunfels, TX · Remote

$50 - $70/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

Dearborn, MI · Remote

$50 - $70/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

Tyler, TX · Remote

$50 - $70/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

Rio Rancho, NM · Remote

$50 - $70/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

Palm Coast, FL · Remote

$50 - $70/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

Newport News, VA · Remote

$50 - $70/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

Coral Springs, FL · Remote

$50 - $70/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

Joliet, IL · Remote

$50 - $70/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

Abilene, TX · Remote

$50 - $70/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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Mhra information

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How much do mhra jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for mhra in the United States is $50.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $61.30 per hour, depending on experience, location, and employer.

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 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.
More about Mhra jobs
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Mhra jobs near you
Infographic showing various Mhra job openings in the United States as of August 2026, with employment types broken down into 24% Full Time, 75% Part Time, and 1% Contract. Highlights an 21% Physical, 1% Hybrid, and 78% Remote job distribution, with an average salary of $104,945 per year, or $50.5 per hour.

Compliance Officers

micro1 AI

Port Saint Lucie, FL • Remote

$50 - $70/hr

Part-time

Posted 8 days ago

Job description

Role Title: Regulatory Affairs Specialist


Role Type: Contractor


Location: Remote


micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review evaluation tasks inspired by real-world agency requests and sponsor response threads, determining if drafted responses meet regulatory expectations.
  2. Apply expert judgment to review clinical documentation, assessing whether conclusions are substantiated, commitments are properly scoped, and records can withstand regulatory scrutiny.
  3. Distinguish between substantively adequate and superficially polished responses, articulating clear rationales for any deficiencies.
  4. Assess consistency across comprehensive document sets, identifying unsupported or conflicting claims within or between documents.
  5. Provide structured, well-reasoned written feedback grounded in applicable regulatory guidelines rather than subjective impressions.
  6. Collaborate asynchronously and communicate complex regulatory concepts clearly in both written and verbal form.


Preferred Qualifications

  1. 5+ years of direct regulatory affairs experience at a sponsor, CRO, or consultancy, with responsibility for clinical submissions.
  2. Documented experience drafting or leading responses to health authority information requests, particularly for ongoing regulatory filings.
  3. 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).
  4. Proven ability to critically read clinical or safety documents to identify regulatory risks, unsupported statements, and potential reviewer concerns.
  5. Exceptional written communication skills, with the capability to convey regulatory reasoning clearly, concisely, and defensibly.
  6. Degree in life sciences, pharmacy, medicine, or a related field; RAC certification is an advantage.
  7. Experience engaging with multiple regions or agencies, prior health authority reviewer/assessor background, or familiarity with AI-assisted regulatory tools (all considered valuable).

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