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Regulatory Affairs Associate Two Jobs (NOW HIRING)

Lancesoft

Regulatory Affairs Associate II

Princeton, NJ · On-site

$50 - $55/hr

Regulatory Affairs Associate II Hybrid working once fully trained. More on site presence whilst training. Role Purpose: Regulatory contractor for data management including data entry, review and ...

Lancesoft

Regulatory Affairs Associate II

Princeton, NJ · On-site

$50 - $55/hr

Regulatory Affairs Associate II Hybrid working once fully trained. More on site presence whilst training. Role Purpose: Regulatory contractor for data management including data entry, review and ...

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 ...

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Regulatory Affairs Associate Two information

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

As of Jun 17, 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 another word for regulatory?

In the context of a Regulatory Affairs Associate, another word for regulatory is compliance or oversight, which refers to ensuring that products and processes meet legal and industry standards. These terms are often used interchangeably when describing the responsibilities of maintaining adherence to regulations and standards in the industry.

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.

What does regulatory mean?

In the context of a Regulatory Affairs Associate Two, 'regulatory' refers to the processes and requirements related to ensuring that products, such as pharmaceuticals or medical devices, comply with government laws and industry standards. This role involves preparing documentation, understanding regulations, and working with agencies to obtain approvals or maintain compliance.

What does regulatory taking mean?

Regulatory taking refers to a situation where government regulations limit the use of private property to such an extent that it effectively deprives the owner of economic value, which can lead to legal disputes. In the context of a Regulatory Affairs Associate, understanding regulatory takings is important for ensuring compliance with property and environmental laws that may impact product approvals or manufacturing processes.

What are examples of regulatory?

Regulatory examples include laws, regulations, and standards that govern the development, approval, and marketing of products such as pharmaceuticals, medical devices, and food. A Regulatory Affairs Associate Two ensures compliance with these requirements, often preparing documentation for regulatory submissions and staying updated on changing regulations.
More about Regulatory Affairs Associate Two jobs
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Regulatory Affairs Associate Two jobs near you
Infographic showing various Regulatory Affairs Associate Two job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, and 2% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% 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

Posted 6 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