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 ...
Regulatory Affairs Specialist
Bedford, MA · On-site
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 ...
Regulatory Affairs Specialist
Bedford, MA · On-site
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 ...
IVD Laboratory Technician
Alpharetta, GA · On-site
$18.50 - $24.75/hr
Familiarity with IVD product development processes and regulatory requirements (NMPA, FDA, IVDR) preferred. Experience * Minimum of 2-3 years of laboratory or R&D experience in the IVD industry ...
IVD Laboratory Technician
Alpharetta, GA · On-site
$18.50 - $24.75/hr
Familiarity with IVD product development processes and regulatory requirements (NMPA, FDA, IVDR) preferred. Experience * Minimum of 2-3 years of laboratory or R&D experience in the IVD industry ...
IVD Laboratory Technician
Alpharetta, GA · On-site
$18.50 - $24.75/hr
Familiarity with IVD product development processes and regulatory requirements (NMPA, FDA, IVDR) preferred. Experience * Minimum of 2-3 years of laboratory or R&D experience in the IVD industry ...
IVD Laboratory Technician
Alpharetta, GA · On-site
$18.50 - $24.75/hr
Familiarity with IVD product development processes and regulatory requirements (NMPA, FDA, IVDR) preferred. Experience * Minimum of 2-3 years of laboratory or R&D experience in the IVD industry ...
Vice President, Regulatory and Head of Regulatory Affairs
San Mateo, CA · On-site
$340K - $370K/yr
Deep expertise in US and international regulatory systems (FDA, EMA, NMPA, PMDA) and familiarity with clinical development processes and requirements * Demonstrated ability to manage complex, cross ...
Vice President, Regulatory and Head of Regulatory Affairs
San Mateo, CA · On-site
$340K - $370K/yr
Deep expertise in US and international regulatory systems (FDA, EMA, NMPA, PMDA) and familiarity with clinical development processes and requirements * Demonstrated ability to manage complex, cross ...
Vice President, Regulatory and Head of Regulatory Affairs
San Mateo, CA · On-site
$340K - $370K/yr
Deep expertise in US and international regulatory systems (FDA, EMA, NMPA, PMDA) and familiarity with clinical development processes and requirements * Demonstrated ability to manage complex, cross ...
Vice President, Regulatory and Head of Regulatory Affairs
San Mateo, CA · On-site
$340K - $370K/yr
Deep expertise in US and international regulatory systems (FDA, EMA, NMPA, PMDA) and familiarity with clinical development processes and requirements * Demonstrated ability to manage complex, cross ...
Vice President, Regulatory and Head of Regulatory Affairs (Foster City)
Foster City, CA · On-site
$340K - $370K/yr
Deep expertise in US and international regulatory systems (FDA, EMA, NMPA, PMDA) and familiarity with clinical development processes and requirements. * Demonstrated ability to manage complex, cross ...
Vice President, Regulatory and Head of Regulatory Affairs (Foster City)
Foster City, CA · On-site
$340K - $370K/yr
Deep expertise in US and international regulatory systems (FDA, EMA, NMPA, PMDA) and familiarity with clinical development processes and requirements. * Demonstrated ability to manage complex, cross ...
IVD Laboratory Technician
Alpharetta, GA · On-site
$18.50 - $24.75/hr
Familiarity with IVD product development processes and regulatory requirements (NMPA, FDA, IVDR) preferred. Experience * Minimum of 2-3 years of laboratory or R&D experience in the IVD industry ...
Quick apply
IVD Laboratory Technician
Alpharetta, GA · On-site
$18.50 - $24.75/hr
Familiarity with IVD product development processes and regulatory requirements (NMPA, FDA, IVDR) preferred. Experience * Minimum of 2-3 years of laboratory or R&D experience in the IVD industry ...
Director, Global CMC Regulatory
$153K - $202K/yr
Interpret and apply global CMC regulatory guidance (FDA, EMA, ICH, PMDA, NMPA, MHRA, etc.) to ensure compliant and efficient regulatory pathways. * Anticipate regulatory risks and proactively develop ...
Director, Global CMC Regulatory
$153K - $202K/yr
Interpret and apply global CMC regulatory guidance (FDA, EMA, ICH, PMDA, NMPA, MHRA, etc.) to ensure compliant and efficient regulatory pathways. * Anticipate regulatory risks and proactively develop ...
Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami ...
Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami ...
Senior Human Factors Engineer
San Diego, CA · On-site
$125 - $150/hr
Familiarity with regulatory standards (FDA Human Factors Guidance, IEC 62366, AAMI HE75, NMPA). * Experience with customer‑facing activities, in‑vitro diagnostics products, and point‑of‑care ...
Senior Human Factors Engineer
San Diego, CA · On-site
$125 - $150/hr
Familiarity with regulatory standards (FDA Human Factors Guidance, IEC 62366, AAMI HE75, NMPA). * Experience with customer‑facing activities, in‑vitro diagnostics products, and point‑of‑care ...
Associate Study Director
Northwood, OH · On-site
FDA, NMPA, ANSM, etc) • Prepares protocol submissions for IACUC review and responds to committee comments/questions as necessary. • Other duties as assigned. Qualifications & Technical ...
Associate Study Director
Northwood, OH · On-site
FDA, NMPA, ANSM, etc) • Prepares protocol submissions for IACUC review and responds to committee comments/questions as necessary. • Other duties as assigned. Qualifications & Technical ...
Associate Director, Statistical Programming
Waltham, MA · Hybrid
$171K - $214K/yr
Strong knowledge of ICH, FDA, EMA, and NMPA regulations and guidelines. * Exceptional interpersonal skills and problem-solving capabilities. * Excellent oral and written communication skills.
Associate Director, Statistical Programming
Waltham, MA · Hybrid
$171K - $214K/yr
Strong knowledge of ICH, FDA, EMA, and NMPA regulations and guidelines. * Exceptional interpersonal skills and problem-solving capabilities. * Excellent oral and written communication skills.
Head of Regulatory Affairs
San Francisco, CA · On-site
$220K - $280K/yr
Experience developing international regulatory strategies, including CE Mark / EU MDR, PMDA (Japan), NMPA (China), and Health Canada * Experience designing real-world evidence strategies and post ...
Head of Regulatory Affairs
San Francisco, CA · On-site
$220K - $280K/yr
Experience developing international regulatory strategies, including CE Mark / EU MDR, PMDA (Japan), NMPA (China), and Health Canada * Experience designing real-world evidence strategies and post ...
$180 - $240/hr
Deep understanding of global regulatory requirements (FDA, ICH, EMA, NMPA). * Strong scientific background with the ability to interpret complex data. * Proficiency with document management systems ...
New
$180 - $240/hr
Deep understanding of global regulatory requirements (FDA, ICH, EMA, NMPA). * Strong scientific background with the ability to interpret complex data. * Proficiency with document management systems ...
New
Experience with regulatory audits and inspections (e.g., FDA, PMDA, NMPA, EMA) is a strong advantage.
Experience with regulatory audits and inspections (e.g., FDA, PMDA, NMPA, EMA) is a strong advantage.
Experience with regulatory audits and inspections (e.g., FDA, PMDA, NMPA, EMA) is a strong advantage.
Quick apply
Experience with regulatory audits and inspections (e.g., FDA, PMDA, NMPA, EMA) is a strong advantage.
Regulatory Affairs Manager
Santa Ana, CA · On-site
$38 - $48/hr
Navigate regulations and standards specific to botanicals and Traditional Chinese Medicine, including the USP Herbal Medicines Compendium, World Health Organization guidance, and China NMPA standards.
Quick apply
Regulatory Affairs Manager
Santa Ana, CA · On-site
$38 - $48/hr
Navigate regulations and standards specific to botanicals and Traditional Chinese Medicine, including the USP Herbal Medicines Compendium, World Health Organization guidance, and China NMPA standards.
Director, Biocompatibility
Saint Paul, MN · On-site
$172K - $344K/yr
Provide expert input for regulatory submissions (IDE, PMA, 510(k), CE, NMPA, etc.) and represent the function during audits and agency interactions. * Maintain strong awareness of evolving global ...
Director, Biocompatibility
Saint Paul, MN · On-site
$172K - $344K/yr
Provide expert input for regulatory submissions (IDE, PMA, 510(k), CE, NMPA, etc.) and represent the function during audits and agency interactions. * Maintain strong awareness of evolving global ...
Director, Biocompatibility
Saint Paul, MN · On-site
$172K - $344K/yr
Provide expert input for regulatory submissions (IDE, PMA, 510(k), CE, NMPA, etc.) and represent the function during audits and agency interactions. * Maintain strong awareness of evolving global ...
Director, Biocompatibility
Saint Paul, MN · On-site
$172K - $344K/yr
Provide expert input for regulatory submissions (IDE, PMA, 510(k), CE, NMPA, etc.) and represent the function during audits and agency interactions. * Maintain strong awareness of evolving global ...
Nmpa information
See salary details
$8.89 - $13.70
16% of jobs
$15.17 is the 25th percentile. Wages below this are outliers.
$13.70 - $18.51
29% of jobs
The median wage is $19.71 / hr.
$18.51 - $23.32
19% of jobs
$27.58 is the 75th percentile. Wages above this are outliers.
$23.32 - $28.13
12% of jobs
$28.13 - $32.93
8% of jobs
$32.93 - $37.74
5% of jobs
$37.74 - $42.55
4% of jobs
$42.55 - $47.36
2% of jobs
$47.36 - $52.16
2% of jobs
$52.16 - $56.97
1% of jobs
$56.97 - $61.78
1% of jobs
$8
$26
$61
How much do nmpa jobs pay per hour?
As of Sep 5, 2026, the average hourly pay for nmpa in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.
What is an NMPA?
NMPA stands for National Medical Products Administration, which is the Chinese regulatory authority responsible for the supervision and regulation of drugs, medical devices, and cosmetics in China. The NMPA evaluates and approves new medical products before they can be marketed, monitors product safety, and enforces quality standards to protect public health. Their work is crucial for ensuring that medical products available in China meet national and international safety and efficacy standards.
What skills and qualifications are needed to thrive as an NMPA?
To thrive as an NMPA, you need a comprehensive understanding of pharmacology, clinical assessment, and relevant healthcare guidelines, often supported by a healthcare degree and specific non-medical prescribing certification. Familiarity with prescribing software, electronic health records, and drug databases is typically required. Strong communication, decision-making, and attention to detail are vital soft skills for effectively managing patient care. These competencies ensure safe, effective medication management and uphold high standards of patient safety and clinical practice.
What are common challenges faced by NMPAs and how can they be addressed?
Professionals in NMPA (National Medical Products Administration) roles often encounter challenges such as navigating complex regulatory requirements, staying updated with frequent policy changes, and ensuring timely approvals for medical products. To address these, it's crucial to maintain strong attention to detail, build collaborative relationships with regulatory colleagues, and participate in ongoing training or professional development. Many NMPA teams operate in fast-paced environments where adaptability and clear communication with cross-functional teams—including R&D, quality assurance, and legal—are key to success.
What is the difference between Nmpa vs Pharmacist?
| Aspect | Nmpa | Pharmacist |
|---|---|---|
| Required Credentials | Certification in medical device or pharmaceutical regulation, often specific to NMPA standards | Doctor of Pharmacy (PharmD) or Bachelor of Pharmacy, state licensure |
| Work Environment | Regulatory agencies, pharmaceutical companies, medical device firms | Hospitals, retail pharmacies, clinics |
| Industry Usage | Regulation and compliance within China’s pharmaceutical and medical device sectors | Dispensing medications, patient counseling, healthcare settings |
While Nmpa professionals focus on regulatory compliance and approval processes within China’s pharmaceutical and medical device industries, pharmacists are healthcare providers responsible for dispensing medications and patient care. Both roles require specialized knowledge but serve different functions in the healthcare and industry sectors.
More about Nmpa jobs
What job categories do people searching Nmpa jobs look for?
The top searched job categories for Nmpa jobs are:
- Biology Degree Cosmetic
- Regulatory Affairs Associate
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- International Affairs Manager
- Entry Level Regulatory Affairs Associate
- Cosmetic Regulatory
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- Freelance Cmc Regulatory Affairs
- Quality Regulatory Manager
- Freelance Pharmaceutical Regulatory Affairs
Full-time
Re-posted 18 days ago
Job description
Responsibilities:
Determine and document change assessments for US Class II devices to ensure compliance with the US regulation. Plan and prepare submissions for US Class II devices, including creating, translating, revising, reviewing, and compiling documents, as well as responding to questions and requests from the FDA.
Determine and document change assessments for US Class II devices to ensure compliance with the US regulation. Plan and prepare submissions for US Class II devices, including creating, translating, revising, reviewing, and compiling documents, as well as responding to questions and requests from the FDA.
- Determine and document change assessments for EU Class III & IIb devices to ensure compliance with the EU Medical Device Regulation.
- Plan and prepare submissions for EU Class III & IIb devices, including creating, translating, revising, reviewing, and compiling documents, as well as responding to questions and requests from the Notified Body.
- Support submission and maintenance of product registrations in markets worldwide.
- Support product registrations, including creating, revising, reviewing and compiling documents for submission to regulatory authorities, as well as assisting in responding to questions and requests from such authorities.
- Assist in external audits by supporting responses to auditor questions and requests.
- Keep abreast of new or changed regulations and standards and perform gap analyses.
- Perform additional duties as assigned.
- (REQUIRED) Bachelor's degree, preferably in the life sciences; advanced degree a plus.
- (REQUIRED) At least 3 years of experience in medical device field, including hands-on experience with submissions.
- 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-driven and electro-mechanical medical devices a plus.
- Strong knowledge of US and international requirements for regulatory submissions and maintenance of medical devices.
- Team player with ability to work independently in hybrid/in-person setting (Bedford, MA).
- Excellent and effective written and verbal communication skills.
- Excellent interpersonal skills, good judgment and analytical skills.
- Effective time management and organizational skills.
- Consistent, quality work and commitment to follow-through.
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008