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 ...
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 ...
Develop and implement a comprehensive, risk-based quality compliance strategy aligned with global regulatory expectations (FDA, EMA, MHRA, ICH). * Provide executive oversight of core quality systems ...
Develop and implement a comprehensive, risk-based quality compliance strategy aligned with global regulatory expectations (FDA, EMA, MHRA, ICH). * Provide executive oversight of core quality systems ...
Director, Clinical Quality and Pharmacovigilance
New York, NY · Remote
$81K - $111K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Quick apply
Director, Clinical Quality and Pharmacovigilance
New York, NY · Remote
$81K - $111K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Senior Director, Quality
Mount Vernon, IN · On-site
Serve as the primary site contact for health authority inspections (e.g., FDA, MHRA); lead responses to inquiries, facilitate investigations, and maintain strong agency relationships. Quality Unit ...
Senior Director, Quality
Mount Vernon, IN · On-site
Serve as the primary site contact for health authority inspections (e.g., FDA, MHRA); lead responses to inquiries, facilitate investigations, and maintain strong agency relationships. Quality Unit ...
Knowledge of GxP systems, risk-based quality management principles, and GCP regulations (FDA, MHRA, EMA, etc.) and guidance documents (GCP/ICH) is required. Experience supporting global clinical ...
Knowledge of GxP systems, risk-based quality management principles, and GCP regulations (FDA, MHRA, EMA, etc.) and guidance documents (GCP/ICH) is required. Experience supporting global clinical ...
Medical writing
Wadsworth, OH · On-site
$150K - $175K/yr
Must Have Technical/Functional Skill Awareness of Regulatory guidelines (PhrMA, IFPMA, USFDA-OPDP, MHRA, EMA etc) for Product promotion, Advertising Standards Council guidelines, Sunshine act ...
Medical writing
Wadsworth, OH · On-site
$150K - $175K/yr
Must Have Technical/Functional Skill Awareness of Regulatory guidelines (PhrMA, IFPMA, USFDA-OPDP, MHRA, EMA etc) for Product promotion, Advertising Standards Council guidelines, Sunshine act ...
Knowledge of GxP systems, risk-based quality management principles, and GCP regulations (FDA, MHRA, EMA, etc.) and guidance documents (GCP/ICH) is required. Experience supporting global clinical ...
Knowledge of GxP systems, risk-based quality management principles, and GCP regulations (FDA, MHRA, EMA, etc.) and guidance documents (GCP/ICH) is required. Experience supporting global clinical ...
Director, Clinical Quality and Pharmacovigilance
New York, NY · On-site
$87K - $119K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Director, Clinical Quality and Pharmacovigilance
New York, NY · On-site
$87K - $119K/yr
FDA, EMA, MHRA etc.), including sponsor pre-approval and pre-license inspections supporting marketing applications (NDA/MAA). * Prepare and support internal teams, sponsors, and/or clinical sites ...
Sr. Specialist, Quality Assurance LMS (Learning Management Systems)
Sanford, NC · On-site
$72K - $99K/yr
... MHRA, Health Canada) and internal audits and function as the Training contact in inspections (FDA, EMA, MHRA, Health Canada) and internal audits. • Ensure electronic Veeva Training system audit ...
Sr. Specialist, Quality Assurance LMS (Learning Management Systems)
Sanford, NC · On-site
$72K - $99K/yr
... MHRA, Health Canada) and internal audits and function as the Training contact in inspections (FDA, EMA, MHRA, Health Canada) and internal audits. • Ensure electronic Veeva Training system audit ...
Maintain accurate training records to support inspections (FDA, EMA, MHRA, Health Canada) and internal audits and function as the Training contact in inspections (FDA, EMA, MHRA, Health Canada) and ...
Maintain accurate training records to support inspections (FDA, EMA, MHRA, Health Canada) and internal audits and function as the Training contact in inspections (FDA, EMA, MHRA, Health Canada) and ...
Senior Director, Quality
Mount Vernon, IN · On-site
Serve as the primary site contact for health authority inspections (e.g., FDA, MHRA); lead responses to inquiries, facilitate investigations, and maintain strong agency relationships. * Quality Unit ...
Senior Director, Quality
Mount Vernon, IN · On-site
Serve as the primary site contact for health authority inspections (e.g., FDA, MHRA); lead responses to inquiries, facilitate investigations, and maintain strong agency relationships. * Quality Unit ...
Previous experience supporting audits and regulatory inspections (e.g., FDA, PMDA, EMA, MHRA). * Thorough understanding of ICH- GCP guidelines and regulatory requirements as they apply to the TMF.
Previous experience supporting audits and regulatory inspections (e.g., FDA, PMDA, EMA, MHRA). * Thorough understanding of ICH- GCP guidelines and regulatory requirements as they apply to the TMF.
Chief Legal Officer
Manhattan, NY · On-site
You will sit on the executive team and report directly to the CEO. The three loads you carry are: keeping the platform compliant with FDA AI/ML guidance, EMA, MHRA, and any emerging AI-disclosure ...
Chief Legal Officer
Manhattan, NY · On-site
You will sit on the executive team and report directly to the CEO. The three loads you carry are: keeping the platform compliant with FDA AI/ML guidance, EMA, MHRA, and any emerging AI-disclosure ...
Ensures medical assessment of individual case safety reports meets highest standards and processes and activities are compliant with ICH, FDA, EMA, MHRA regulations. * Provides guidance and ...
Ensures medical assessment of individual case safety reports meets highest standards and processes and activities are compliant with ICH, FDA, EMA, MHRA regulations. * Provides guidance and ...
The successful candidate will bring deep expertise in global quality and regulatory requirements (FDA, EMA, MHRA, PMDA, TGA, Health Canada, and other applicable health authorities) for stability and ...
The successful candidate will bring deep expertise in global quality and regulatory requirements (FDA, EMA, MHRA, PMDA, TGA, Health Canada, and other applicable health authorities) for stability and ...
Ensures medical assessment of individual case safety reports meets highest standards and processes and activities are compliant with ICH, FDA, EMA, MHRA regulations. * Provides guidance and ...
Ensures medical assessment of individual case safety reports meets highest standards and processes and activities are compliant with ICH, FDA, EMA, MHRA regulations. * Provides guidance and ...
Experience in regulatory submissions to medical device regulatory bodies a plus; e.g., FDA, Health Canada, ANVISA/INMETRO, EU NB, MHRA, Swissmedic, NMPA, PMDA, MFDS, and TGA. * Experience with ...
Experience in regulatory submissions to medical device regulatory bodies a plus; e.g., FDA, Health Canada, ANVISA/INMETRO, EU NB, MHRA, Swissmedic, NMPA, PMDA, MFDS, and TGA. * Experience with ...
Experience in regulatory submissions to medical device regulatory bodies a plus; e.g., FDA, Health Canada, ANVISA/INMETRO, EU NB, MHRA, Swissmedic, NMPA, PMDA, MFDS, and TGA. * Experience with ...
Experience in regulatory submissions to medical device regulatory bodies a plus; e.g., FDA, Health Canada, ANVISA/INMETRO, EU NB, MHRA, Swissmedic, NMPA, PMDA, MFDS, and TGA. * Experience with ...
Lead inspection readiness and management for regulatory authority inspections (FDA, EMA, MHRA, PMDA); serve as primary QA contact, coordinate responses to observations, and oversee regulatory ...
Quick apply
Lead inspection readiness and management for regulatory authority inspections (FDA, EMA, MHRA, PMDA); serve as primary QA contact, coordinate responses to observations, and oversee regulatory ...
Senior Director, Quality
Mount Vernon, IN · On-site
Serve as the primary site contact for health authority inspections (e.g., FDA, MHRA); lead responses to inquiries, facilitate investigations, and maintain strong agency relationships. * Quality Unit ...
Senior Director, Quality
Mount Vernon, IN · On-site
Serve as the primary site contact for health authority inspections (e.g., FDA, MHRA); lead responses to inquiries, facilitate investigations, and maintain strong agency relationships. * Quality Unit ...
Mhra information
See salary details
$15.87 - $21.28
3% of jobs
$21.28 - $26.70
3% of jobs
$26.70 - $32.12
3% of jobs
$32.12 - $37.54
8% of jobs
$39.98 is the 25th percentile. Wages below this are outliers.
$37.54 - $42.96
16% of jobs
$42.96 - $48.38
9% of jobs
The median wage is $50.58 / hr.
$48.38 - $53.80
17% of jobs
$58.95 is the 75th percentile. Wages above this are outliers.
$53.80 - $59.22
16% of jobs
$59.22 - $64.64
8% of jobs
$64.64 - $70.06
7% of jobs
$70.06 - $75.48
8% of jobs
$15
$50
$75
How much do mhra jobs pay per hour?
As of Sep 1, 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 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?
| Aspect | Mhra | Pharmacist |
|---|---|---|
| Required Credentials | Regulatory knowledge, compliance certifications | Pharmacy degree, licensing, registration |
| Work Environment | Regulatory agencies, pharmaceutical companies | Community pharmacies, hospitals, clinics |
| Employer & Industry Usage | Health authorities, pharmaceutical industry | Healthcare 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.
More about Mhra jobs
What states have the most Mhra jobs?
States with the most job openings for Mhra jobs include:
What job categories do people searching Mhra jobs look for?
The top searched job categories for Mhra jobs are:
Contractor
Re-posted 15 days ago
Job description
Company Description
MEDVACON Life Sciences works with many leading pharmaceutical companies to hire contractors for projects & assignments in cGMP Quality, Compliance, Validation and CSV work.
We're supporting our client in Foster City CA to hire contractors for several roles. This is an outstanding opp to work with colleagues across different therapy areas and functional teams (Clinical Operations, Business Conduct, etc)
Job Description
- 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 SOPs and other procedural documents.
- Participates in developing and presenting training using standard modules and training on compliance related topics.
- Participates in the periodic assessment and review of Medical Affairs GxP role-based training plans to suggest improvements to existing curriculums.
- Assists in audit readiness for regulatory agency inspections
- Supports Medical Affairs with internal or external routine audit activities and document reviews.
- Ability to work hybrid if local to the site only - NO Full remote
Qualifications
Exp in a pharma Medial Affairs lead role.
Ability to work W2 only
$45 ph
Excellent written/oral communication skills.
Solid organizational & planning skills.
Excellent problem-solving skills
Additional Information
Please attach a WORD resume to your submission
All of your information will be kept confidential according to EEO guidelines.
ON-SITE only on W2
This is a contract role and does not offer benfits
40-hour week