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Regulatory Operations Jobs in Edison, NJ (NOW HIRING)

Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and Regulatory (MLR) groups. This position will ...

As an integral member of Otsuka's regulatory operations team, providesregulatory publishing and submissionassignments, monitoring,andoversight, as well as alead orsupport for GRA efforts * Ensures ...

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Regulatory Operations information

See Edison, NJ salary details

$11

$27

$55

How much do regulatory operations jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for regulatory operations in Edison, NJ is $27.17, according to ZipRecruiter salary data. Most workers in this role earn between $18.41 and $31.35 per hour, depending on experience, location, and employer.

What do regulatory operations do?

Regulatory operations professionals manage the processes and systems involved in preparing, submitting, and maintaining regulatory documents for product approvals and compliance. They ensure that regulatory submissions meet legal requirements, often using specialized software and working closely with cross-functional teams such as R&D, quality, and legal. Their work supports the timely approval and ongoing compliance of products in regulated industries like pharmaceuticals and medical devices.

What are common day-to-day responsibilities for professionals in regulatory operations?

Regulatory Operations professionals are primarily responsible for preparing, formatting, and submitting regulatory documents to health authorities, ensuring they meet stringent compliance standards. They coordinate with cross-functional teams—such as clinical, quality, and legal departments—to gather and verify required information. Daily tasks often include managing document workflows, maintaining regulatory databases, and tracking submission timelines. This role requires close attention to regulatory updates and an ability to quickly adapt processes in response to changing requirements.

What are the key skills and qualifications needed to thrive in regulatory operations, and why are they important?

To excel in Regulatory Operations, candidates should have a strong understanding of regulatory guidelines, documentation processes, and compliance standards—often supported by a degree in life sciences, pharmacy, or a related field. Familiarity with electronic document management systems (EDMS), submission publishing tools, and possibly certifications such as Regulatory Affairs Certification (RAC) are commonly expected. Excellent attention to detail, project management, and effective communication skills enable individuals to coordinate across teams and ensure timely submissions. These competencies are critical for maintaining compliance, minimizing risk, and supporting the efficient approval of products in highly regulated industries.

What is a regulatory operations job?

A Regulatory Operations job involves managing the submission and compliance processes required for regulatory approval of products, typically in industries like pharmaceuticals, biotechnology, and medical devices. Responsibilities include formatting and submitting regulatory documents, ensuring compliance with global regulations, and maintaining submission lifecycle management. This role often requires collaboration with cross-functional teams, expertise in regulatory guidelines, and proficiency in regulatory submission systems such as eCTD.

What are popular job titles related to Regulatory Operations jobs in Edison, NJ? For Regulatory Operations jobs in Edison, NJ, the most frequently searched job titles are:
What job categories do people searching Regulatory Operations jobs in Edison, NJ look for? The top searched job categories for Regulatory Operations jobs in Edison, NJ are:
What cities near Edison, NJ are hiring for Regulatory Operations jobs? Cities near Edison, NJ with the most Regulatory Operations job openings:
Infographic showing various Regulatory Operations job openings in Edison, NJ as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $56,513 per year, or $27.2 per hour.

Regulatory Operations Specialist

Omnicom

New York, NY • On-site

$65K - $80K/yr

Full-time

Posted 12 days ago


Job description

Agency:
Omnicom Precision Marketing
Job Function:
Production
Job Subfunction:
Production Operations
Job Description:
MRM is part of the Omnicom Precision Marketing activation practice. This practice integrates CRM platform expertise, journey management, and first-party data capabilities with creative excellence and performance capabilities, enabling Omnicom to deliver intelligent activation across the full funnel with data-driven decisioning at scale to help clients move faster and deliver more connected customer experiences.
MRM is a modern relationship marketing agency dedicated to building enduring brand relationships. MRM's specialized capabilities drive relationship lifetime value and span CRM, Customer Experience, and Commerce with data and martech at the core. MRM operates in a borderless, integrated way to enable greater collaboration, creativity, and true speed to market. For more information, please visit www.mrm.com.
The Regulatory Operations Specialist position is an integral part of MRM Health and the Regulatory Operations capability. Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and Regulatory (MLR) groups.
This position will support the Princeton pharmaceutical/health Client base. The Regulatory Operations Specialist will manage submission workflow and capacity for specific brands and work to achieve expert level status on Client regulatory submission, collaboration, and archive platforms/tools. This includes a supporting role in adhering to and maintaining processes and requirements for the capability.
Responsibilities:
- Serve as day-to-day submissions lead; manage and filter workload to team members
- Demonstrate general knowledge of Regulatory Affairs and guidelines that govern advertising and promotional material according to FDA
- Work cross functionally with Project Management to ensure submission timelines are met and all material is gathered for accurate and timely submissions
- Learn client-based submission systems and be able to navigate for efficient use, including the tagging and linking of references based on annotations provided by Copy team
- Maintain reference library and asset library for internal cross-functional use
- Execute submissions in the following manner:
- Initiate the submission process
- Track the project from kickoff through to final submission Client MLR approval
- Organize submission materials in accordance with the Client dictated requirements
- Ensure integrity of submission materials to ensure adherence with Client MLR requirements
- Submit materials via Client MLR submission platform/tool
- Provide status updates on submission progresses
- Support team with prepping and sending final samples, and 2253 materials when needed
- Record keeping and knowledge base:
- Document and maintain project tracker
- Document and maintain current Client requirements for MLR submission
- Maintain knowledge of the Client MLR schedule
- Utilize and maintain regulatory document control and appropriate distribution of regulatory documents
Education and Experience:
- 2 -4 years of experience in a relatable role preferred
- Familiarity with agency submission process and MLR preferred
- Strong interpersonal and problem-solving skills; be able to build strong relationships within the agency and client organizations, and must be able to participate in client and internal agency meetings with senior personnel
- Ability to manage multiple projects as one cohesive program
- Capacity for risk identification and management
- Strong sense of ownership of process and results
- Strong writing and verbal skills
- High-level of organization and detail with an ability to influence others in these areas
- Ability to find creative solutions to complex problems and multi-task
- Must be comfortable working in an environment that utilizes electronic docbases, databases, and computer systems (Microsoft Office, Veeva Vault, Zinc, and web based applications)
- Experience and competence in MS Office
- Workload management and people supervisory experience a plus
This position will be based in New York City. The salary range for this position is $65,000 to $80,000. Where an employee or prospective employee is paid within this range will depend on, among other factors, actual ranges for current/former employees in the subject position; the associated discipline; market considerations; budgetary considerations; tenure and standing with the company (applicable to current employees); as well as the employee's/applicant's background, pertinent experience, and qualifications$65,000-$80,000
Omnicom's policy requires employees to work in the office for a minimum of three days a week, unless additional in-office days are directed by their agency or manager. Our objective is to increase this requirement over time, and many of our agencies as well as Omnicom's corporate group already require five days of in-office attendance.
Omnicom is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we're focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us-we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice.
Link to Recruitment Privacy Notice: https://www.omc.com/privacy-notice
For US Job Seekers:
It is the policy of Omnicom and any of its affiliates to provide equal employment opportunities to all employees and applicants for employment without regard to race, religion, color, ethnic origin, gender, gender identity, age, marital status, veteran status, sexual orientation, disability, or any other basis prohibited by applicable federal, state, or local law. EOE/AA/M/D/V/F.