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Nmpa Jobs (NOW HIRING)

CorDx

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 ...

CorDx

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 ...

CorDx

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 ...

Gateway Recruiting

VP of Trade Compliance

Sunnyvale, CA

$147K - $197K/yr

Understanding FDA-regulated products and global equivalents (EU MDR, UKCA, PMDA, NMPA, ANVISA, etc.). Governance, Policy, and Risk Management: * Establish and maintain global policies covering: HS ...

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 Behring

GRA CMC Specialist

King Of Prussia, PA

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 ...

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 ...

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How much do nmpa jobs pay per hour?

As of Jun 4, 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 are the key skills and qualifications needed to thrive as an NMPA (Non-Medical Prescribing Associate), and why are they important?

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 some common challenges faced by professionals working in NMPA roles 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 are NMPA and what do they do?

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 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.

More about Nmpa jobs
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 May 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.
IVD Laboratory Technician

IVD Laboratory Technician

CorDx

Alpharetta, GA • On-site

$18.50 - $24.75/hr

Full-time

Medical, Retirement, PTO

Posted 18 days ago

Job description

About Us

CorDx, a multi-national biotech organization, focused on pushing the limits of innovation and supply in global health. With over 2000 employees across the world serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious diseases such as COVID-19, pregnancy, drug abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.

Key Responsibilities1. Laboratory & Technical Responsibilities
  • Perform laboratory testing and experimentation related to lateral flow (chromatographic) diagnostic products, including but not limited to assay preparation, testing, troubleshooting, and optimization.
  • Execute routine and non-routine testing to support product development, verification, validation, and performance evaluation.
  • Accurately document experimental procedures, observations, and results in laboratory notebooks, controlled forms, and electronic systems in compliance with quality system requirements.
  • Assist in reagent preparation, sample handling, equipment calibration, and laboratory maintenance.
2. Product Design & Development Support
  • Support various stages of the IVD product design and development process, from feasibility and prototyping through verification and validation.
  • Collaborate with R&D, Quality, and Regulatory teams to ensure development activities comply with applicable sections of ISO 13485 and 21 CFR Part 820 (Quality System Regulation).
  • Contribute to design inputs, design outputs, risk management activities, and design change documentation as required.
3. Evaluation Protocols & Performance Testing
  • Execute testing activities in accordance with Evaluation Protocol (EP) documents for analytical and clinical performance evaluation.
  • Apply EPs to assess performance characteristics such as sensitivity, specificity, accuracy, precision, reproducibility, robustness, and stability.
  • Support data analysis and summary reporting for internal reviews, regulatory submissions, and design history file (DHF) documentation.
4. Quality & Compliance
  • Follow Good Documentation Practices (GDP) and laboratory best practices.
  • Adhere to CorDx quality policies, standard operating procedures (SOPs), and safety requirements.
  • Participate in audits, inspections, and internal reviews as needed.

Requirements

Education
  • Bachelor’s degree or higher in Biology, Medical Laboratory Science, Biotechnology, or a closely related field.
Technical Skills
  • Strong understanding of biological laboratory operations, experimental procedures, and common laboratory instruments.
  • Ability to design experiments, perform data analysis, interpret results, and independently complete technical reports.
  • Proficiency in scientific literature search and interpretation.
  • 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 preferred.

Benefits

  • Comprehensive medical insurance.
  • 401(k) plan with company contributions.
  • Flexible paid time off (PTO) policy.