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Regulatory Affairs Assistant Jobs (NOW HIRING)

Research applicable regulations, standards, and guidance documents and summarize findings for review * Assist with reviewing and writing SOPs and other Regulatory Affairs policies as necessary

New

NY · On-site

$56 - $76/hr

Primary Purpose ofJob Assess and support regulatory compliance and the quality of service deliverysystems. Assist in the development and implementation of Regulatory Affairs related staff training ...

New

Job Title: Regulatory Affairs Manager - Mass Markets South Location: Remote (Austin, Houston ... * Assist in drafting regulatory comments, filings, responses, and supporting documentation as ...

Primary Purpose of Job Assess and support regulatory compliance and the quality of service delivery systems. Assist in the development and implementation of Regulatory Affairs related staff training ...

NY · On-site

$75 - $95/hr

# Regulatory Affairs SpecialistZdrowie i urodaBobrowiecka, Warszawa +2 Lokalizacje## PolpharmaPełny ... Assist in developing and implementing regulatory strategies for new and existing products*

New

Job Title: Regulatory Affairs Manager - Mass Markets South Location: Remote (Austin, Houston ... * Assist in drafting regulatory comments, filings, responses, and supporting documentation as ...

Regulatory Affairs Specialist 1 Year Contract Warsaw, IN (100% Onsite) Duties Responsible for ... Respond to requests from foreign government and/or distributors as needed Assist with the research ...

$70 - $90/hr

Regulatory Affairs Specialist 1 Year Contract Warsaw, IN (100% Onsite) Duties Responsible for ... Respond to requests from foreign government and/or distributors as needed * Assist with the ...

New

Regulatory Affairs Associate Location: South Portland, ME Duration: 12 Months Shifts: 8AM TO 4:30PM ... Strategic Planning: Assist in SOP development, review and initiation; Stay abreast of regulatory ...

Regulatory Affairs Specialist 1 Year Contract Warsaw, IN (100% Onsite) Duties Responsible for ... Respond to requests from foreign government and/or distributors as needed * Assist with the ...

Duties and Responsibilities * Assist the Regulatory Affairs Manager (RAM) with the maintenance and upkeep of registration and listings for each of the sterilization sites. * Perform activities for ...

Showing results 21-40

Regulatory Affairs Assistant information

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$15

$34

$145

How much do regulatory affairs assistant jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for regulatory affairs assistant in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What is a regulatory affairs assistant?

Regulatory Affairs Assistants are professionals who support regulatory affairs teams in ensuring that companies comply with all relevant laws and regulations related to their products, such as pharmaceuticals, medical devices, or food products. Their responsibilities typically include preparing and submitting documentation to regulatory bodies, maintaining records, tracking regulatory changes, and assisting in audits or inspections. They play a crucial role in helping organizations bring products to market efficiently and legally, while minimizing compliance risks. This entry-level position is foundational for a career in regulatory affairs and requires attention to detail, organizational skills, and an understanding of regulatory requirements.

How does a regulatory affairs assistant typically interact with other departments within a company?

Regulatory Affairs Assistants often work closely with various departments such as research and development, quality assurance, and manufacturing. Their main responsibility is to help ensure that all product documentation and submissions comply with relevant regulations, which requires gathering information and coordinating updates from these teams. Effective communication and collaboration are essential, as Regulatory Affairs Assistants may attend cross-functional meetings and serve as a liaison to clarify regulatory requirements. This interdepartmental interaction helps streamline the approval process and ensures products meet compliance standards before reaching the market.

What are the key skills and qualifications needed to thrive as a regulatory affairs assistant, and why are they important?

To thrive as a Regulatory Affairs Assistant, you need a solid understanding of regulatory guidelines, attention to detail, and a degree in life sciences or a related field. Familiarity with document management systems, regulatory submission software, and databases like eCTD is typically required. Strong organizational skills, effective communication, and the ability to work well under deadlines are essential soft skills. These competencies ensure accurate and timely submissions, compliance with regulations, and effective support of regulatory teams.

What is the difference between Regulatory Affairs Assistant vs Regulatory Affairs Specialist?

AspectRegulatory Affairs AssistantRegulatory Affairs Specialist
CredentialsTypically requires a bachelor's degree in life sciences or related fieldRequires a bachelor's degree, often with additional certifications or experience
Work EnvironmentSupports regulatory teams, handles documentation, and assists with submissionsLeads regulatory strategies, reviews submissions, and interacts with authorities
Industry UsageCommonly employed in pharmaceutical, biotech, and medical device companiesMore senior role, but overlaps in industry and employer types

The main difference is that Regulatory Affairs Assistants support and perform administrative tasks within regulatory teams, while Regulatory Affairs Specialists take on more responsibility in strategy, review, and communication with regulatory agencies. The Assistant role is often an entry-level position, whereas the Specialist role requires more experience and expertise.

How to get into regulatory affairs with no experience?

Regulatory Affairs Assistants often start with a bachelor's degree in life sciences, pharmacy, or related fields. Gaining knowledge of regulations through online courses or certifications and developing skills in document management and attention to detail can improve chances; internships or entry-level roles in healthcare or compliance also provide valuable experience.

Is regulatory affairs high paying?

Regulatory affairs assistants typically earn moderate salaries, with pay increasing with experience, certifications, and the complexity of the industry they work in. While entry-level positions may have lower pay, experienced professionals or those in specialized sectors can earn higher wages, especially with advanced knowledge of regulations and compliance tools.
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What states have the most Regulatory Affairs Assistant jobs?

States with the most job openings for Regulatory Affairs Assistant jobs include:

Infographic showing various Regulatory Affairs Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

$68K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Key responsibilities

  • Support company registrations and device listings in domestic and international markets.

  • Assist with preparing and maintaining regulatory documentation and submissions, including technical files and regulatory filings such as 510(k).

  • Coordinate with cross-functional teams regarding product changes, regulatory notifications, and compliance requirements.


Job description

Job Summary:

 

Zymo Research is looking for a motivated individual to join our Regulatory Affairs team! In this role, you will play a vital part in supporting regulatory activities and maintaining compliance with applicable requirements, utilizing your skills and expertise in regulatory documentation, coordination, and compliance support. Your contributions will help ensure high-quality, compliant regulatory processes that support Zymo Research.

The Regulatory Affairs Associate is an entry-level position for an individual committed to developing a career in Regulatory Affairs. The role supports Regulatory Affairs activities primarily for Zymo Research and may also support affiliated companies as business needs require, with training and guidance from experienced Regulatory Affairs personnel.

Join us in making a meaningful impact!

Essential Duties and Responsibilities

 

  • Support company registrations and device listings in domestic (U.S.) and international markets
  • Support preparation and maintenance of IVDD/IVDR technical documentation and registrations
  • Support product registrations and regulatory submissions to FDA and other regulatory bodies including 510(k) submissions as applicable
  • Research applicable regulations, standards, and guidance documents and summarize findings for review
  • Assist with reviewing and writing SOPs and other Regulatory Affairs policies as necessary
  • Coordinate with cross functional teams regarding product changes and regulatory notification and/or approval requirements
  • Perform initial reviews of marketing materials, labels, and public communications for regulatory compliance under guidance
  • Assist with evaluating product compliance with applicable regulations and project requirements
  • Assist with and participate in notified body audits, ISO registrar audits, government inspections, customer audits, and other audits or regulatory activities as needed.
  • Support Regulatory Affairs projects across Zymo Research and affiliated companies and perform other related duties as business needs require

Education and Experience:

 

  • Bachelor's degree in a science or related discipline preferred. Entry-level candidates and recent graduates are encouraged to apply; prior Regulatory Affairs experience is not required.
  • Demonstrated interest in developing a long-term career in Regulatory Affairs.
  • Positive, collaborative, and professional attitude with a strong willingness to learn and contribute to the team.
  • Demonstrates initiative, ownership, and willingness to take on new responsibilities and unfamiliar assignments as learning opportunities.
  • Flexible and adaptable, with the ability to research and work through regulatory questions that may require interpretation, judgment, and guidance.
  • Highly organized and efficient, with strong attention to detail, time management, and ability to prioritize multiple tasks.
  • Ability to work independently when appropriate, use MS Office to organize information for reports and presentations, and handle confidential information with professional integrity.


About Us:

 

Since its inception in 1994, Zymo Research has been proudly serving the scientific community by providing innovative, reliable, and high-quality research tools and products. Whether it's DNA, RNA, epigenetics, microbiomics, protein, or yeast-based research, our philosophy remains the same: To provide the highest quality products in the industry while ensuring they are both simple to use and reliable in their performance.

Recognized as a Top Workplace by the Orange County Register in 2021, 2022, and named a Top Workplace USA in 2023, Zymo Research continues to be a vibrant community where employees thrive, feel connected, and are inspired by their work. If you are passionate about contributing to scientific advancement and want to be part of an exceptional team in a dynamic, growing company, we'd love to hear from you!

 

Compensation, Benefits, and Perks:                                 

The estimated base compensation range for this position is $68,000-75,000 at the time of posting. Actual compensation details will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors.

Zymo Research also offers competitive benefits and perks including:

  • Medical, Dental, Vision, and Life Insurance Coverages
  • EAP Sessions
  • Vacation Time plus Company Holidays
  • Paid Sick Leave
  • Generous 401(K) with matching 
  • Employee Referral Bonus
  • Complimentary fruit, snacks, and beverages
  • Complimentary catered lunches on Thursdays 
  • Complimentary EV Charging 
  • Cell phone stipend


Equal Employment Opportunity Employer:

Zymo Research welcomes candidates of all backgrounds. These include sex, age, color, race, religion, marital status, national origin, ancestry, sexual orientation, gender, gender identity, gender expression, physical & mental disability, medical condition, genetic information, military and veteran status, or any other protected status as defined by federal, state, or local law.

 

Location:

Onsite - Zymo Research Operations - 2961 Dow Ave, Tustin, CA, 92780

Disclaimer: At Zymo, we take the integrity of our hiring process seriously. Please be aware of fraudulent recruitment activities that may use our name to deceive job seekers. We will never ask for payment, sensitive personal information, or financial details during the recruitment process.

All legitimate communications will come from an official Zymo or TriNet Hiring email address. If you are contacted by anyone claiming to represent us using a free email service (e.g., Gmail, Yahoo, Hotmail) or asking for payment, please treat this as fraudulent and report it immediately to careers@zymoresearch.com