Product Security Engineer
Raleigh, NC · On-site
Support Regulatory Affairs and Quality Assurance with global regulatory submissions (e.g., US FDA, EU MDR, China NMPA) by providing product security subject matter expertise. * Review system ...
Raleigh, NC · On-site
Support Regulatory Affairs and Quality Assurance with global regulatory submissions (e.g., US FDA, EU MDR, China NMPA) by providing product security subject matter expertise. * Review system ...
Raleigh, NC · On-site
Support Regulatory Affairs and Quality Assurance with global regulatory submissions (e.g., US FDA, EU MDR, China NMPA) by providing product security subject matter expertise. * Review system ...
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.
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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.
Experience with regulatory audits and inspections and IR (e.g., FDA, PMDA, NMPA, EMA) is a strong advantage.
Experience with regulatory audits and inspections and IR (e.g., FDA, PMDA, NMPA, EMA) is a strong advantage.
Ensure compliance with applicable global regulations and standards, including GLP, GMP, FDA, EMA, ICH, OECD, NMPA, and other relevant regulatory requirements. * Provide strategic quality oversight of ...
Ensure compliance with applicable global regulations and standards, including GLP, GMP, FDA, EMA, ICH, OECD, NMPA, and other relevant regulatory requirements. * Provide strategic quality oversight of ...
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 ...
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 ...
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 ...
Wauwatosa, WI · On-site
Works with a cross functional team to prepare and submit regulatory submissions such as MDR EU Technical Files, or submissions to other global regulators such as NMPA, TGA, etc., for the purpose of ...
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Wauwatosa, WI · On-site
Works with a cross functional team to prepare and submit regulatory submissions such as MDR EU Technical Files, or submissions to other global regulators such as NMPA, TGA, etc., for the purpose of ...
Oro Valley, AZ · On-site
$25.50/hr
Accurately performs tasks in a regulated environment (OSHA, NMPA, FDA, etc.). Performs and documents all transactions and production instructions with accuracy related to the proper receipt ...
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Oro Valley, AZ · On-site
$25.50/hr
Accurately performs tasks in a regulated environment (OSHA, NMPA, FDA, etc.). Performs and documents all transactions and production instructions with accuracy related to the proper receipt ...
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 ...
$174K - $230K/yr
Maintain deep expertise in global diagnostic regulations (FDA, EU IVDR, PMDA, NMPA, etc.) and assess impact on development and registration activities. * Monitor evolving regulatory landscape and ...
$174K - $230K/yr
Maintain deep expertise in global diagnostic regulations (FDA, EU IVDR, PMDA, NMPA, etc.) and assess impact on development and registration activities. * Monitor evolving regulatory landscape and ...
Ensure timely and compliant processing and reporting of ICSRs to Health Authorities (e.g., FDA, Health Canada, NMPA, etc.) and business partners. * Oversee operational performance and workload ...
Ensure timely and compliant processing and reporting of ICSRs to Health Authorities (e.g., FDA, Health Canada, NMPA, etc.) and business partners. * Oversee operational performance and workload ...
Redmond, WA · On-site
$150K - $230K/yr
Contribute to global regulatory strategy including FDA, IVDR, and NMPA * Support transition from RUO/LDT assays to IVD companion diagnostics * Ensure diagnostic strategy supports precision medicine ...
Redmond, WA · On-site
$150K - $230K/yr
Contribute to global regulatory strategy including FDA, IVDR, and NMPA * Support transition from RUO/LDT assays to IVD companion diagnostics * Ensure diagnostic strategy supports precision medicine ...
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 ...
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 ...
Westlake Village, CA · On-site
$100K - $130K/yr
Prepare, review, and submit and provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA, TGA ...
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Westlake Village, CA · On-site
$100K - $130K/yr
Prepare, review, and submit and provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA, TGA ...
Westlake Village, CA · On-site
$100K - $130K/yr
Prepare, review, and submit and provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA, TGA ...
Westlake Village, CA · On-site
$100K - $130K/yr
Prepare, review, and submit and provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA, TGA ...
IVDR, FDA, NMPA) impacting Clinical LC-MS adoption. Qualifications Education: Degree in Life Sciences, Chemistry, Engineering, or related scientific discipline. Advanced degree (Master's or PhD ...
IVDR, FDA, NMPA) impacting Clinical LC-MS adoption. Qualifications Education: Degree in Life Sciences, Chemistry, Engineering, or related scientific discipline. Advanced degree (Master's or PhD ...
Redmond, WA · On-site
$90K - $140K/yr
NMPA/CDE requirements (China), where applicable * IVDR (EU), as relevant * Support preparation of regulatory documentation, including: * IDE/IND biomarker sections * CDx bridging strategies (RUO/LDT ...
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Redmond, WA · On-site
$90K - $140K/yr
NMPA/CDE requirements (China), where applicable * IVDR (EU), as relevant * Support preparation of regulatory documentation, including: * IDE/IND biomarker sections * CDx bridging strategies (RUO/LDT ...
Morrisville, NC · On-site
$106K - $146K/yr
Support Regulatory Affairs and Quality Assurance with global regulatory submissions (e.g., US FDA, EU MDR, China NMPA) by providing product security subject matter expertise. * Review system ...
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Morrisville, NC · On-site
$106K - $146K/yr
Support Regulatory Affairs and Quality Assurance with global regulatory submissions (e.g., US FDA, EU MDR, China NMPA) by providing product security subject matter expertise. * Review system ...
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 ...
Thousand Oaks, CA · On-site
$157K - $208K/yr
Lead strategy development, preparation, and cross-functional alignment for key Health Authority interactions (FDA, EMA, PMDA, NMPA, etc.) related to metabolic disorders, including protocol advice, CV ...
Thousand Oaks, CA · On-site
$157K - $208K/yr
Lead strategy development, preparation, and cross-functional alignment for key Health Authority interactions (FDA, EMA, PMDA, NMPA, etc.) related to metabolic disorders, including protocol advice, CV ...
$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
| 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.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 6 days ago
Sourced by ZipRecruiter
Medical equipment and supplies manufacturing
10,000+ Employees
Tempe, AZ, US
1997