In-depth knowledge of US FDA regulations, ISO standards, MHRA and EU regulations (including Annex 11), and ICH guidelines and Drug Development Life Cycle process. Extensive experience developing and ...
In-depth knowledge of US FDA regulations, ISO standards, MHRA and EU regulations (including Annex 11), and ICH guidelines and Drug Development Life Cycle process. Extensive experience developing and ...
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 ...
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 ...
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 software ...
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 software ...
Program Director HRA
Bronx, NY · On-site
Extensive knowledge of principles and practices of HIV/AIDS Program guidelines and the HRA, MHRA and HPD regulations and directives, as applicable to the Program. Ability to provide emergency ...
Program Director HRA
Bronx, NY · On-site
Extensive knowledge of principles and practices of HIV/AIDS Program guidelines and the HRA, MHRA and HPD regulations and directives, as applicable to the Program. Ability to provide emergency ...
Clinical Quality Auditor
South San Francisco, CA · On-site
$60 - $75/hr
Experience with MHRA and Health Canada regulations * Familiarity with Veeva and/or Smartsheets * Strong communication, collaboration, and stakeholder management skills INDBH #LI-MG1
Clinical Quality Auditor
South San Francisco, CA · On-site
$60 - $75/hr
Experience with MHRA and Health Canada regulations * Familiarity with Veeva and/or Smartsheets * Strong communication, collaboration, and stakeholder management skills INDBH #LI-MG1
Alarm Management Technician
Frederick, MD · On-site
$23 - $25/hr
Stay current with regulatory requirements (e.g., GMP, FDA, MHRA) related to alarm management and pharmaceutical operations. * Participate in emergency response drills and support real-time emergency ...
Quick apply
Alarm Management Technician
Frederick, MD · On-site
$23 - $25/hr
Stay current with regulatory requirements (e.g., GMP, FDA, MHRA) related to alarm management and pharmaceutical operations. * Participate in emergency response drills and support real-time emergency ...
Alarm Management Technician
Frederick, MD · On-site
$22 - $25/hr
Stay current with regulatory requirements (e.g., GMP, FDA, MHRA) related to alarm management and pharmaceutical operations. * Participate in emergency response drills and support real-time emergency ...
Quick apply
Alarm Management Technician
Frederick, MD · On-site
$22 - $25/hr
Stay current with regulatory requirements (e.g., GMP, FDA, MHRA) related to alarm management and pharmaceutical operations. * Participate in emergency response drills and support real-time emergency ...
Senior Director - Quality GCP
Boston, MA · On-site
Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus. * Able to provide solution ...
Senior Director - Quality GCP
Boston, MA · On-site
Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus. * Able to provide solution ...
Alarm Management Technician
Frederick, MD · On-site
$23 - $25/hr
Stay current with regulatory requirements (e.g., GMP, FDA, MHRA) related to alarm management and pharmaceutical operations. * Participate in emergency response drills and support real-time emergency ...
Quick apply
Alarm Management Technician
Frederick, MD · On-site
$23 - $25/hr
Stay current with regulatory requirements (e.g., GMP, FDA, MHRA) related to alarm management and pharmaceutical operations. * Participate in emergency response drills and support real-time emergency ...
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 ...
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 ...
Senior Director Quality GCP
Boston, MA · On-site
$185K - $235K/yr
Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus. * Able to provide solution ...
Senior Director Quality GCP
Boston, MA · On-site
$185K - $235K/yr
Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus. * Able to provide solution ...
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Quick apply
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Quick apply
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Senior Director - Quality GCP
Boston, MA · On-site
$185K - $235K/yr
Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus. * Able to provide solution ...
Senior Director - Quality GCP
Boston, MA · On-site
$185K - $235K/yr
Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus. * Able to provide solution ...
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Quick apply
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Quick apply
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Quick apply
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Field Property Technician - Construction & Maintenance
Auburn, ME · On-site
$21.25 - $29/hr
Consistent with the provisions of the Americans With Disabilities Act (ADA) and the Maine Human Rights Act (MHRA), and other States' disability laws, applicants may request accommodations needed to ...
Field Property Technician - Construction & Maintenance
Auburn, ME · On-site
$21.25 - $29/hr
Consistent with the provisions of the Americans With Disabilities Act (ADA) and the Maine Human Rights Act (MHRA), and other States' disability laws, applicants may request accommodations needed to ...
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Quick apply
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
Quick apply
QA Product Manager (Sterile Products)
Florham Park, NJ · Remote
$45 - $59/hr
Strong knowledge of regulatory requirements and guidelines, such as FDA, EMA, MHRA, PIC/S, ICH, and sterility assurance standards. System One, and its subsidiaries including Joulé and Mountain Ltd ...
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?
What is an MHRA inspector?
What kind of projects or responsibilities can a new MHRA inspector expect during their first year on the job?
What are the key skills and qualifications needed to thrive as an MHRA regulatory affairs specialist, and why are they important?
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.
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:

Job description
Lead Quality Assurance resource needed to provide quality support for global computer validation projects in the ERP area, such as SAP, under the guidance of the Global Quality Computer Compliance team.
Job duties will include:
- Reviewing and providing input to validation and test strategies
- Verify documentation is in compliance with internal procedures and external regulations
- Participate in review and approval of requirements, test scripts, reports and other SDLC documentation with a focus on quality, and testability
- In addition, the resource may be pulled to support other programs of the following as needed:
- Participate in process changes in the organization
- Participate in audits
- Participate in change management of additional systems
Education/Training/Work Experience:
The position requires a Bachelor's Degree in Engineering or Sciences with a minimum of 5-8 years experience working in life sciences industry with focus in the area of Quality Assurance.
Experience working with various GxP Enterprise Computerized Systems (on-premise and Cloud based (SaaS) COTS) used in the life sciences industry. Candidate must be well-versed with Software Development Life Cycle (SDLC) methodologies such as Waterfall and V-model. In-depth knowledge of US FDA regulations, ISO standards, MHRA and EU regulations (including Annex 11), and ICH guidelines and Drug Development Life Cycle process. Extensive experience developing and using risk based approaches for computer systems validation. Experience in managing multiple projects and determined to get job done correctly and on time.
All your information will be kept confidential according to EEO guidelines.
About LanceSoft
Sourced by ZipRecruiter
Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.
Industry
Recruiting and staffing services
Company size
1,001 - 5,000 Employees
Headquarters location
Herndon, VA, US
Year founded
2000