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Nmpa Jobs (NOW HIRING)

NAMSA

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 Competencies:

Sironax Ltd.

Medical Writing Director

Waltham, MA · On-site

$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

Revance

Regulatory Device Specialist

Johnson City, TN · On-site

$65K - $73K/yr

... NMPA (China), MFDS (South Korea), COFEPRIS (Mexico), SFDA (Saudi Arabia), and MOHAP (UAE). * Prepare and manage export and country-specific documentation, including Certificates to Foreign Government ...

CSL

GRA CMC Specialist

King Of Prussia, PA · On-site

Monitor, interpret, and communicate evolving global CMC regulations (FDA, EMA, PMDA, NMPA, etc.). Ensure timely dissemination of regulatory intelligence to internal stakeholders and integration into ...

CSL Plasma Inc.

$180 - $240/hr

Monitor, interpret, and communicate evolving global CMC regulations (FDA, EMA, PMDA, NMPA, etc.). * Ensure timely dissemination of regulatory intelligence to internal stakeholders and integration ...

New

CRISPR Therapeutics

$170 - $190/hr

Partner with Regulatory Affairs on safety‑related regulatory submissions and health authority queries (FDA, EMA, PMDA/MHLW, NMPA/CDE) * Provide medical safety training to case processing staff ...

ZEISS

Senior Supplier Quality Expert

Hebron, KY · On-site

Lead quality governance for distribution and wholesale, ensuring compliance with EU GMP, 21 CFR 210/211/820/111, ISO 13485, EU MDR, NMPA/SAMR, EFSA, DSHEA, ICH, and other standards. * Establish and ...

CSL Plasma Inc.

GRA CMC Specialist

Waltham, MA · On-site

$180 - $240/hr

Monitor, interpret, and communicate evolving global CMC regulations (FDA, EMA, PMDA, NMPA, etc.). * Ensure timely dissemination of regulatory intelligence to internal stakeholders and integration ...

New

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How much do nmpa jobs pay per hour?

As of Sep 6, 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?

AspectNmpaPharmacist
Required CredentialsCertification in medical device or pharmaceutical regulation, often specific to NMPA standardsDoctor of Pharmacy (PharmD) or Bachelor of Pharmacy, state licensure
Work EnvironmentRegulatory agencies, pharmaceutical companies, medical device firmsHospitals, retail pharmacies, clinics
Industry UsageRegulation and compliance within China’s pharmaceutical and medical device sectorsDispensing 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.

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What job categories do people searching Nmpa jobs look for?

The top searched job categories for Nmpa jobs are:

Nmpa jobs near you
Infographic showing various Nmpa job openings in the United States as of August 2026, with employment types broken down into 99% Full Time, and 1% Contract. Highlights an 66% Physical, 14% Hybrid, and 20% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.

Associate Study Director

NAMSA

Northwood, OH • On-site

Full-time

Re-posted 29 days ago

Key responsibilities

  • Assist in the coordination of study conduct tasks from study initiation to study completion.

  • Perform noncomplex studies and serve as the primary contact for the client, keeping them informed of schedule and issues.

  • Ensure project compliance with applicable quality system regulations and NAMSA SOPs, and serve as Study Director for GLP and non-GLP preclinical studies.

NAMSA rating

8.3

Company rating: 8.3 out of 10

Based on 16 frontline employees who took The Breakroom Quiz

37th of 121 rated laboratories

Job description

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.

We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry's premier provider. We provide support for clients during every step of the product development lifecycle and beyond.

Come and work for an organization with the:

Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the

Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core

Values:

  • Act with integrity in everything we do.

  • Provide best-in-class customer experiences.

  • Develop superior talent and deliver expertise.

  • Respond with agility and provide timely results.

  • Embrace collaboration, diverse perspectives and ideas.

Job Description:

Assists in the coordination of study conduct tasks from study initiation to study completion.
Performs noncomplex studies and serves as the primary contact for the client, as assigned, and keeps the client informed of schedule and any unforeseen events or issues.
Performs project in compliance with applicable quality system regulations (i.e. ISO, GMP, GLP) and NAMSA SOPs.
Knows and understands the Animal Welfare Requirements and serves as Principal Investigator, when applicable.
Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed.
May need to participate in study specific procedures.
Evaluates, analyzes and interprets data and presents in a clear, well-organized, scientifically sound report.
Assures that all data including unanticipated responses are accurately recorded, verified and organized.
May need to ensure that study records for GLP studies are archived upon completion of the study.
May need to interact with regulatory bodies (i.e. FDA, NMPA, ANSM, etc)
Prepares protocol submissions for IACUC review and responds to committee comments/questions as necessary.
Other duties as assigned.

Qualifications & Technical Competencies:

Medical device research or pathology experience preferred.
Requires a minimum of a Bachelor's degree, preferably in a scientific discipline, with a minimum of 1 year of related laboratory experience.

Working Conditions:

While performing the duties of this job, the Associate is regularly exposed to general office conditions, and will be required to regularly work on personal computers and keyboards. The Associate is frequently exposed to a variety of livestock, domestic and laboratory animals and to fluoroscopy and faxitron x-ray imaging. The Associate is occasionally exposed to sharp objects, radioactive isotopes, gasses such as CO2 and isoflurane, toxic or caustic chemicals, and a Bio-Safety-Level 2 (BSL2) environment. On rare occasions, the Associate may be exposed to zoonotic diseases and blood borne pathogens.
The noise level in the work environment is usually moderate.
While performing the duties of this job, the Associate is regularly required to sit, stand, walk, use hands and fingers, reach with hands and arms, talk and hear, use computer keyboard, and view computer monitors. The Associate must occasionally lift and/or move up to 50 pounds.
Specific vision abilities required by this job include close vision, the ability to adjust focus, exceptional spatial acuity and visual-kinesthetic coordination.

NAMSA is an equal employment opportunity company. NAMSA participates in pre-employment background and drug screen processes aligned to local, state and federal laws.

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