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What are the key skills and qualifications needed to thrive as a PMDA (Pharmaceuticals and Medical Devices Agency) 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 PMDA and what do they do?

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 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 some common challenges faced by a PMDA (Project Management Data Analyst), 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 are popular job titles related to Pmda jobs in Virginia? For Pmda jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Pmda jobs in Virginia look for? The top searched job categories for Pmda jobs in Virginia are:
What cities in Virginia are hiring for Pmda jobs? Cities in Virginia with the most Pmda job openings:
Pmda jobs near you
Infographic showing various Pmda job openings in Virginia as of July 2026, with employment types broken down into 95% Full Time, and 5% Part Time. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution.
Pharmaceutical Operator

Pharmaceutical Operator

Afton Scientific, LLC

Charlottesville, VA • On-site

$25 - $30/hr

Full-time

Posted 27 days ago

Job description

Afton Scientific is a contract manufacturing organization (CMO) in Virginia that specializes in small-batch filling of injectables from clinical trials to approved commercial drugs.
Utilizing 35,000 Sq. Ft of manufacturing, lab, warehouse, and administrative space, Afton provides custom, innovative solutions for clinical to commercial sterile manufacturing, packaging and labeling, analytical and micro lab services, and pharmaceutical support services.
Our Ready-To-Fill® line continues with our philosophy of guidance and support for our clients. It offers top-quality pre-sterilized components to those who can fill in-house.
  • Serving clients in 18 Countries
  • Successful NDA and ANDA drug registrations
  • In good standing with the FDA, PMDA, and MHRA

NOTE: Afton Scientific does not sponsor work visas. No recruiters please.
Pay Details: Non-exempt position, range of $25 - $30 per hour, depending on level of experience.
Essential Functions:
1. Perform manufacturing processes and operate production equipment, including, but not limited to: washers, autoclave, dry heat oven, heat sealers, vial washer, ultrasonic cleaner.
2. Perform production operations according to Batch Records and Standard Operating Procedures (SOPs)
3. Maintain proper documentation (batch records, production logs, etc.)
4. Write and review master documents as applicable: SOPs and batch records
5. Write Operation Deviation Reports
6. Supervise contract production employees as applicable
7. Maintain inventory of control warehouse space
8. Perform production and maintenance activities in the Aseptic Processing Area (APA)
9. Write and edit documents including: procedures, deviations, master batch records, protocols and reports as necessary
10. Perform initial assembly and review of completed production records for completeness
11. Maintain order and cleanliness in production area
Knowledge, Skills & Abilities
1. Ability to read and write English. Dress, speak and act in a professional manner
2. Physically able to stand for extended periods of time, mover objects up to 50 pounds, bend and reach to access equipment, have near vision correctable to 20/20 and be able to wear corrective eyewear to achieve this, if necessary.
3. Must be capable of working in close proximity to other employees, regardless of gender, in the confined environment of the production facility.
4. Must be capable of working in the clean room for uninterrupted extended periods
5. Ability to maintain neat and accurate records required
6. Must be able to work with minimal supervision.
Requirements for Education and Experience
1. Minimum of high school diploma or GED; Associates or Bachelor's degree desirable
2. One year of manufacturing experience required. Three years manufacturing experience or more strongly preferred.
3. Clean room experience preferred.

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