ZipRecruiter

Log In

1

Regulatory Affairs Associate Two Jobs (NOW HIRING)

Stark Pharma Solutions Inc

IL · On-site

I am working on Regulatory Affairs Associate I position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed is as follows. Job ...

AstraZeneca

Regulatory Affairs Associate

Santa Clara, CA · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

next page

Showing results 1-20

All JobsRegulatory Affairs Associate Two Jobs

Regulatory Affairs Associate Two information

See salary details

$18

$39

$62

How much do regulatory affairs associate two jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for regulatory affairs associate two in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What is the difference between Regulatory Affairs Associate Two vs Regulatory Affairs Associate One?

AspectRegulatory Affairs Associate TwoRegulatory Affairs Associate One
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, entry-level certifications may suffice
Work EnvironmentMid-level regulatory team, more independent responsibilitiesEntry-level, supervised tasks within regulatory teams
Employer & Industry UsagePharmaceutical, biotech, medical device companiesSimilar industries, often within larger regulatory departments
Common Search & Comparison IntentUnderstanding role progression and responsibilitiesEntry-level position details and requirements

The main difference between Regulatory Affairs Associate Two and Regulatory Affairs Associate One lies in experience and responsibilities. Associate Two typically has more experience, handles more complex tasks independently, and may require relevant certifications. Associate One is an entry-level role focused on foundational regulatory tasks. Both roles are common in the pharmaceutical and biotech industries, with Associate Two representing a more advanced position within the regulatory team.

Is regulatory affairs a stable career?

Regulatory affairs is generally considered a stable career due to consistent demand in industries like pharmaceuticals, medical devices, and biotechnology. Professionals in this field often require specialized knowledge of regulations and may hold certifications, which support long-term employment opportunities.
More about Regulatory Affairs Associate Two jobs
What cities are hiring for Regulatory Affairs Associate Two jobs? Cities with the most Regulatory Affairs Associate Two job openings:
What states have the most Regulatory Affairs Associate Two jobs? States with the most job openings for Regulatory Affairs Associate Two jobs include:
What job categories do people searching Regulatory Affairs Associate Two jobs look for? The top searched job categories for Regulatory Affairs Associate Two jobs are:
Regulatory Affairs Associate Two jobs near you
Infographic showing various Regulatory Affairs Associate Two job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Affairs Associate - II

Fladger Associates

Foster City, CA • On-site

Contractor

Re-posted 26 days ago

Job description

Foster City, CA
Contract Duration: 12-18 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Regulatory Affairs Associate II in the Foster City, CA area. (Onsite Role)
  • Contractor must meet the company site requirements for the COVID Vaccination PRIOR to starting role
  • Responsible for the preparation of Drug Listings/Lot Distribution Reports (Biologics)
  • Responsible for compiling documentation and sending Certificate of Pharmaceutical Product (CPP) requests to FDA
  • Manage Notarizations (CA licensed notary public a plus), Legalization/apostille of regulatory documents
  • Assist in documentation and signature preparation for:
    • License renewals
    • Establishment registration
  • Performs document filing and retrieval functions as directed, or in conjunction with departmental SOPs and work instructions and direction of a senior Regulatory Affairs professional.
  • Performs workflows and procedures regarding document tracking, indexing and retrieving, and disseminating information to the Regulatory Affairs CMC department.
  • Seeks assistance from appropriate internal and external resources.
  • Participates in preparing regulatory submissions under direction of a senior Regulatory Affairs Professional which require some interactions with other members in the Regulatory department for investigational and commercial products in line with US and ICH requirements, regional requirements and scientific and company policies and procedures.
  • Works to develop and acquire required regulatory skills and knowledge, with guidance from immediate supervisor.
  • Assist with miscellaneous US RA CMC team-related administrative documents/activities such as processing of invoices.
  • Participates in group meetings and provides tactical approaches to addressing issues of moderate complexity and seeks assistance from appropriate internal and external resources.

Experience:

  • A Bachelor's Degree with a minimum of 2+ years of relevant training or industry experience preferably in a GMP environment, OR 1+ years relevant training or industry experience preferably in GMP environment with advanced degree.
  • Must work well under deadlines and have excellent attention to detail.
  • Strong computer and organizational skills required.
  • Excellent verbal and written communication skills and interpersonal skills are required.
  • Preferred:
    • Degree in a relevant Scientific field
    • Relevant Regulatory CMC submission experience