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Full Time Pharmaceutical Regulatory Affairs Jobs

Regulatory Specialist

Lake Zurich, IL · On-site

$100.71K - $110.42K/yr

Must have a Bachelor's degree in Chemistry, Biochemistry, Biology, Biotechnology or related field and one (1) year of experience in pharmaceutical regulatory affairs or other scientific area ...

Regulatory Specialist

Lake Zurich, IL · Hybrid

$100.71K - $110.42K/yr

Must have a Bachelor's degree in Chemistry, Biochemistry, Biology, Biotechnology or related field and one (1) year of experience in pharmaceutical regulatory affairs or other scientific area ...

Regulatory Affairs Specialist We are currently seeking a detail-oriented and motivated Regulatory ... Bachelor's degree in a related field such as biology, chemistry, or pharmaceutical sciences.

NJ · On-site

... pharmaceutical regulatory affairs (mandatory) Attention to detail Excellent oral and written ... communication skills Knowledge of US drug regulatory requirements (mandatory) REQUIRED BS or MS in ...

Bachelor's degree in a related field such as biology, chemistry, or pharmaceutical sciences ... Previous experience in a regulatory affairs role within the pharmaceutical industry is preferred.

Role Description This is a full-time on-site role for a Regulatory Affairs Specialist located in ... Pharmacies * Bachelor's degree in a relevant field (pharmacy, biology, chemistry, etc.

Medical Affairs Employment Type: Full Time Location: Austin, TX Description Who We Are Powered by ... or pharmaceuticals preferred). * Demonstrated experience preparing and managing regulatory ...

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Full Time Pharmaceutical Regulatory Affairs information

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How much do full time pharmaceutical regulatory affairs jobs pay per hour?

As of May 28, 2026, the average hourly pay for full time pharmaceutical regulatory affairs in the United States is $56.97, according to ZipRecruiter salary data. Most workers in this role earn between $42.07 and $66.59 per hour, depending on experience, location, and employer.

What is the difference between Full Time Pharmaceutical Regulatory Affairs vs Full Time Pharmaceutical Quality Assurance?

AspectFull Time Pharmaceutical Regulatory AffairsFull Time Pharmaceutical Quality Assurance
Primary FocusEnsuring compliance with regulations, preparing submissions, and maintaining regulatory documentationMaintaining product quality, implementing quality systems, and conducting audits
Required CredentialsBachelor's in pharmacy, life sciences, or related field; regulatory certificationsBachelor's in pharmacy, chemistry, or related; quality management certifications
Work EnvironmentRegulatory agencies, pharmaceutical companies, documentation-heavy tasksManufacturing sites, quality labs, compliance departments
Industry UsageCommonly searched for regulatory compliance rolesOften compared in quality management contexts

Full Time Pharmaceutical Regulatory Affairs focuses on navigating regulatory requirements and submissions, while Full Time Pharmaceutical Quality Assurance emphasizes maintaining product quality and compliance through audits and quality systems. Both roles require related credentials and are integral to pharmaceutical industry success, but they serve distinct functions within the product lifecycle.

What cities are hiring for Full Time Pharmaceutical Regulatory Affairs jobs? Cities with the most Full Time Pharmaceutical Regulatory Affairs job openings:
What are the most commonly searched types of Pharmaceutical Regulatory Affairs jobs? The most popular types of Pharmaceutical Regulatory Affairs jobs are:
What states have the most Full Time Pharmaceutical Regulatory Affairs jobs? States with the most job openings for Full Time Pharmaceutical Regulatory Affairs jobs include:

Remote Regulatory Affairs Consultant - Biosimilars

Apsida Life Science

Manhattan, NY • Remote

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

A leading life science consulting firm is seeking a Pharmaceutical Regulatory Consultant to provide regulatory expertise in drug development. The candidate will be responsible for interpreting FDA requirements, investigating patent expiry timelines, and translating legal frameworks into insights for teams. This fully remote role requires a bachelor's degree in Life Sciences or Pharmacy and at least 5 years of regulatory affairs experience.

Offers competitive compensation and a work-life balance. #J-18808-Ljbffr