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Pmda Jobs in California (NOW HIRING)

AccuScan Sciences

Head of Product Management

Milpitas, CA · On-site

$271K - $284K/yr

Support regulatory and reimbursement strategies, including work related to MolDx, IVDR, and PMDA. * Drive global market strategy. * Coordinate cross-functional execution from development through ...

AccuScan Sciences

Head of Product Management

Milpitas, CA · On-site

$271K - $284K/yr

Support regulatory and reimbursement strategies, including work related to MolDx, IVDR, and PMDA. * Drive global market strategy. * Coordinate cross-functional execution from development through ...

AccuScan Sciences

Head of Product Management

Milpitas, CA · On-site

$271K - $284K/yr

Support regulatory and reimbursement strategies, including work related to MolDx, IVDR, and PMDA. * Drive global market strategy. * Coordinate cross-functional execution from development through ...

micro1 AI

Regulatory Affairs Specialist

Carlsbad, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Vista, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Regulatory Affairs Specialist

Concord, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Garden Grove, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Oakland, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Compliance Officers

Palmdale, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

micro1 AI

Regulatory Affairs Specialist

Antioch, CA · Remote

$50 - $80/hr

Demonstrated working knowledge of the ICH framework, CTD/eCTD structure, and practical expectations of at least one major regulatory body (FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to ...

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Pmda information

What is a PMDA?

PMDA stands for Pharmaceuticals and Medical Devices Agency, which is a Japanese government agency responsible for reviewing, approving, and monitoring pharmaceuticals, medical devices, and regenerative medicines. They ensure the safety, efficacy, and quality of these products before and after they enter the Japanese market. PMDA also provides consultation services during the development process and post-marketing surveillance to protect public health.

What are the key skills and qualifications needed to thrive as a PMDA reviewer, and why are they important?

To thrive as a PMDA reviewer, you need an advanced degree in pharmaceutical sciences, medicine, or related fields, along with a thorough understanding of drug development and regulatory requirements. Familiarity with regulatory submission systems, guideline databases, and scientific data analysis tools is essential. Strong analytical thinking, attention to detail, and effective communication are critical soft skills for this role. These competencies ensure rigorous evaluation of medical products, safeguard public health, and facilitate clear interactions with stakeholders.

What are some common challenges faced by a PMDA, and how can they be addressed?

One common challenge for a PMDA is balancing the need for timely project updates with ensuring data accuracy and consistency across multiple sources. Since PMDAs often work with cross-functional teams, aligning everyone on standardized data reporting processes can be demanding. Building strong communication channels and implementing robust data validation tools can help overcome these challenges. Additionally, proactively seeking feedback from stakeholders and regularly updating documentation can streamline workflows and support project success.

What is the difference between Pmda vs Pharmacist?

AspectPmdaPharmacist
Required CredentialsTypically requires a specialized certification or training in medical device regulationRequires a pharmacy degree and licensure
Work EnvironmentRegulatory agencies, medical device companies, healthcare complianceCommunity pharmacies, hospitals, healthcare settings
Industry UsageRegulatory and compliance sectors within healthcarePharmaceuticals, healthcare, patient care

While Pmda professionals focus on medical device regulation and compliance, pharmacists are licensed healthcare providers specializing in medication dispensing and patient care. Both roles are vital in healthcare but serve different functions and require distinct credentials.

What are popular job titles related to Pmda jobs in California?

For Pmda jobs in California, the most frequently searched job titles are:

What job categories do people searching Pmda jobs in California look for?

The top searched job categories for Pmda jobs in California are:

What cities in California are hiring for Pmda jobs?

Cities in California with the most Pmda job openings:

Pmda jobs near you
Infographic showing various Pmda job openings in California as of August 2026, with employment types broken down into 42% Full Time, 57% Part Time, and 1% Contract. Highlights an 21% Physical, 5% Hybrid, and 74% Remote job distribution.

Head of Product Management

Milpitas, CA • On-site

AccuScan Sciences
See more jobs at AccuScan Sciencesexternal

$271K - $284K/yr

Full-time

Re-posted 18 days ago

Job description

AccuScan Sciences is a liquid biopsy biotechnology company developing whole-genome sequencing solutions for minimal residual disease detection in oncology. The team is focused on turning complex clinical and genomic insights into products that can support more informed cancer care and broaden the impact of precision diagnostics.

In this role, you will shape product strategy for a growing oncology portfolio, helping connect scientific innovation, clinical evidence, and market needs. You will work across internal teams and external stakeholders to guide how products are defined, positioned, and advanced in regulated global markets.

Responsibilities
  • Define the product roadmap for MRD assays across multiple indications.
  • Translate clinical data into product requirements, claims, and market positioning.
  • Support regulatory and reimbursement strategies, including work related to MolDx, IVDR, and PMDA.
  • Drive global market strategy.
  • Coordinate cross-functional execution from development through launch.
  • Engage key opinion leaders, partners, and consortia to inform product direction.

Requirements

  • 8+ years of product management experience in oncology diagnostics or molecular diagnostics.
  • Experience launching regulated IVD or LDT products across global markets.
  • Strong knowledge of MRD and liquid biopsy, with experience in clinical evidence strategy.
  • Experience working with MolDx, IVDR, and PMDA.
  • Proven ability to interface effectively with key opinion leaders, commercial leadership, regulatory teams, reimbursement teams, and external partners.
  • Must be eligible to work in the United States.
  • A PhD or MBA is a plus.

Apply