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Remote Biomedical Regulatory Affairs Jobs in Rutherford, NJ

Director, Regulatory Affairs

New York, NY ยท On-site +1

$164K - $216K/yr

We are seeking a Director of Regulatory Affairs who will play a critical role in supporting global ... This role is remote-friendly, with most work conducted from home. There may be occasional ...

Director, CMC Regulatory Affairs

New York, NY ยท Remote

$207K - $255K/yr

The Team You'll Join As Director CMC Regulatory Affairs, you will be an essential member of the ... This role is remote-friendly, with most work conducted from home. There may be occasional ...

Director, US Regulatory Affairs

Morristown, NJ ยท On-site +1

$154K - $204K/yr

Depending upon location, this role will be hybrid or remote and will require some travel as ... This position reports to the Vice President, Regulatory Affairs. Essential Functions: * High-level ...

Biomedical Engineering Tutor

Clifton, NJ ยท Remote

$18 - $40/hr

... and regulatory affairs. Ability to explain signal processing for biosignals, finite element ... Familiar with biomedical engineering curricula and common challenges such as integrating biology ...

... and regulatory affairs. Ability to explain signal processing for biosignals, finite element ... Familiar with biomedical engineering curricula and common challenges such as integrating biology ...

... and regulatory affairs. Ability to explain signal processing for biosignals, finite element ... Familiar with biomedical engineering curricula and common challenges such as integrating biology ...

Biomedical Engineering Tutor

Summit, NJ ยท Remote

$18 - $40/hr

... and regulatory affairs. Ability to explain signal processing for biosignals, finite element ... Familiar with biomedical engineering curricula and common challenges such as integrating biology ...

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Remote Biomedical Regulatory Affairs information

See Rutherford, NJ salary details

$19

$40

$63

How much do remote biomedical regulatory affairs jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for remote biomedical regulatory affairs in Rutherford, NJ is $40.34, according to ZipRecruiter salary data. Most workers in this role earn between $32.36 and $47.79 per hour, depending on experience, location, and employer.

What is the difference between Remote Biomedical Regulatory Affairs vs Remote Biomedical Quality Assurance?

AspectRemote Biomedical Regulatory AffairsRemote Biomedical Quality Assurance
Required credentialsLife sciences degree, regulatory certifications (e.g., RAC)Quality management certifications (e.g., CQE, ISO auditor)
Work environmentCollaborates with regulatory agencies, documentation reviewEnsures product quality, audits, compliance checks
Employer usagePharmaceutical, biotech, medical device companiesManufacturers, medical device firms, healthcare organizations
Search intentRegulatory submissions, compliance strategiesProduct quality, process improvements

Remote Biomedical Regulatory Affairs focuses on navigating regulatory requirements and submissions, while Remote Biomedical Quality Assurance emphasizes maintaining product quality and compliance through audits and process controls. Both roles are essential in the biomedical industry and often overlap but serve distinct functions.

What are popular job titles related to Remote Biomedical Regulatory Affairs jobs in Rutherford, NJ? For Remote Biomedical Regulatory Affairs jobs in Rutherford, NJ, the most frequently searched job titles are:
What cities near Rutherford, NJ are hiring for Remote Biomedical Regulatory Affairs jobs? Cities near Rutherford, NJ with the most Remote Biomedical Regulatory Affairs job openings:

Director - CMC Regulatory Affairs (Gene Therapy)

Stark Pharma Solutions Inc

Piscataway, NJ โ€ข Remote

$153K - $202K/yr

Contractor

Posted 27 days ago


Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Director โ€“ CMC Regulatory Affairs position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Role: Director โ€“ CMC Regulatory Affairs (Gene Therapy)

Location: Remote (Anywhere in the U.S.)
ย 

We're looking for an experienced Director โ€“ CMC Regulatory Affairs to join a well-funded, mid-sized Gene Therapy Biotech organization with a strong pipeline and proven success.

Key Responsibilities

  • Lead CMC Regulatory Affairs strategy for gene therapy programs.
  • Author and review CMC sections for regulatory submissions (INDs, BLAs, amendments, and global filings).
  • Collaborate with CMC, Manufacturing, Quality, and Regulatory teams to ensure compliant submissions.
  • Support interactions with regulatory agencies and drive submission readiness.
  • Provide strategic regulatory guidance throughout product development and commercialization.

Required Qualifications

  • Extensive experience in CMC Regulatory Affairs within the biotechnology or pharmaceutical industry.
  • Hands-on experience authoring CMC regulatory content (not just reviewing submissions).
  • Strong knowledge of FDA and global regulatory requirements for biologics/gene therapy products.
  • Experience supporting INDs, BLAs, and other regulatory submissions.
  • Excellent communication, leadership, and cross-functional collaboration skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you. ย 

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates:ย https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email:ย karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com