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Mhra Jobs (NOW HIRING)

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 ...

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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Mhra information

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$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?

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.

More about Mhra jobs

What states have the most Mhra jobs?

States with the most job openings for Mhra jobs include:

Infographic showing various Mhra job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, 1% Part Time, 1% Temporary, and 3% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $104,945 per year, or $50.5 per hour.

Quality Assurance Compliance Specialist

LanceSoft Inc

Rockaway, NJ

Full-time

Re-posted 26 days ago


Job description

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.



Specialized Knowledge and Skills: Knowledge in SAP is a plus. In addition, Microsoft Office experience (Word, Excel, PowerPoint). Experience with Microsoft SharePoint is also recommended. Good organization skills and strong interpersonal skills as well as ability to work with other departments. 
Additional Information

All your information will be kept confidential according to EEO guidelines.


LanceSoft logo

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

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