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Regulatory Science Jobs in Ohio (NOW HIRING)

AtriCure

Regulatory Affairs Specialist

Mason, OH · On-site

Bachelor's degree in a technical/scientific/life science discipline required or 3+ years of Regulatory experience in the medical device industry * Proficient on programs within Microsoft Office

F. Hoffmann-La Roche AG

$104 - $139/hr

Bachelor's Degree in Life Sciences, Regulatory Affairs, or a related field * 5 to 10 years of experience in Regulatory Affairs ( Regulatory, R&D, Quality and/or Clinical), with some experience in ...

prince

Color Science Specialist

Ashtabula, OH

This full-time position, Color Science Technician, will be proficient in the completion of Color ... Complies with safety rules and regulations, attends safety meetings and training. * Active support ...

Nationwide Children's Hospital

Coordinates the regulatory and compliance process of all clinical research conducted in the NCH/RI ... Bachelor's degree or equivalent experience in medical/science field. Licensure Requirement: (not ...

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How much do regulatory science jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for regulatory science in Ohio is $47.59, according to ZipRecruiter salary data. Most workers in this role earn between $33.12 and $49.38 per hour, depending on experience, location, and employer.

What is regulatory science?

A Regulatory Science job involves evaluating and developing scientific methods to assess the safety, efficacy, and quality of medical products, food, and other regulated items. Professionals in this field work at the intersection of science, policy, and regulation to ensure compliance with government standards. They may collaborate with regulatory agencies, industry stakeholders, and researchers to facilitate product approvals and post-market surveillance.

What are the typical responsibilities of a regulatory science professional?

Regulatory Science professionals are responsible for ensuring that products comply with regulations throughout all development and commercialization stages. Their daily activities may include preparing and submitting regulatory documents, collaborating with R&D, quality assurance, and legal teams, and interpreting updates to regulations or guidelines that affect product approval. They may also interact directly with regulatory agencies and participate in strategic meetings to help guide product development decisions. Working in Regulatory Science often means being a key liaison between internal teams and regulatory authorities to facilitate smooth approvals and ongoing compliance.

What are the key skills and qualifications needed to thrive in regulatory science?

To thrive in Regulatory Science, you need a solid background in life sciences or a related field, strong analytical and research skills, and familiarity with regulatory frameworks. Experience with regulatory submission systems (like eCTD), knowledge of global regulations, and certifications such as RAC (Regulatory Affairs Certification) can be highly advantageous. Excellent attention to detail, problem-solving abilities, and strong cross-functional communication are critical for success in this field. These competencies ensure regulatory compliance and efficient product development while minimizing delays and risks for organizations bringing products to market.

What can you do with a regulatory science degree?

A regulatory science degree prepares individuals for roles in regulatory affairs, compliance, and policy within industries such as pharmaceuticals, biotechnology, and medical devices. Graduates can work as regulatory specialists, managers, or consultants, often utilizing knowledge of regulations, safety standards, and documentation processes to ensure products meet legal requirements and facilitate approval processes.

What does a regulatory scientist do?

A regulatory scientist evaluates and ensures that products such as pharmaceuticals, medical devices, or food meet government regulations and safety standards. They analyze data, prepare documentation for regulatory submissions, and stay informed about evolving policies, often using scientific and regulatory tools to support product approval and compliance.

What are popular job titles related to Regulatory Science jobs in Ohio?

For Regulatory Science jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Regulatory Science jobs in Ohio look for?

The top searched job categories for Regulatory Science jobs in Ohio are:

What cities in Ohio are hiring for Regulatory Science jobs?

Cities in Ohio with the most Regulatory Science job openings:

Regulatory Science jobs near you
Infographic showing various Regulatory Science job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $98,992 per year, or $47.6 per hour.

Manager of Regulatory Affairs

Mason, OH • On-site

Aprecia Pharmaceuticals, LLC
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Aprecia Pharmaceuticals, LLCexternal

Full-time

Re-posted 7 days ago

Job description

General Purpose of Position:
Responsible for the preparation, review, and submission of regulatory filings (e.g. original NDAs/ANDAs, annual reports, supplements, CBEs (Changes Being Effected), protocols, etc.), tracking and updating status reports for drug product registrations.Regulatory responsibilities also include post-approval drug product reporting activities such as completing regulatory impact assessments for commercial drug product changes, filing labeling and promotional material submissions, supporting adverse event reporting activities and developing appropriate regulatory strategies to support business objectives.
Primary Duties and Responsibilities (Essential Functions):
Duties/Responsibilities 1 Work with Product Development, Technical Services, Analytical, Project Management, Quality Assurance and other staff contributing to the preparation of CMC (Chemistry, Manufacturing, and Controls) and/or clinical, and regulatory submissions. 2 Develop regulatory submission timelines, eCTD (electronic Common Technical Dossier) submission content plans and table of contents, as necessary. 3 Ensure that all eCTD submissions and sections are consistent with regulatory requirements, internal submission criteria, and format standards as necessary for US and international drug product registration applications. 4 Prepare, author, and review regulatory submissions for regulatory compliance, accuracy, and quality.Examples include IND (Investigational New Drug Application), NDA (New Drug Application), PAS (Prior Approval Supplement), AR (Annual Report), and regulatory meeting briefing packages. 5 Remain current with existing and developing FDA regulations, review new regulatory guidance documents and associated regulatory information, and inform RA and other staff regarding applicability and impact of emerging regulations. 6 Review and approve technical and scientific protocols, reports, change controls, and other GMP documents for the RA department. 7 Complete regulatory impact assessments for commercial drug product changes and develop regulatory strategies to support business objectives. 8 Manage development and revisions to Aprecia product labeling. Ensure labeling is kept current with 505(b)(2) Listed Drugs as necessary. 9 Participate in Medical, Legal and Regulatory (MLR) team reviews for Aprecia drug product advertising and promotional materials.Provide regulatory approval of labeling and promotional materials in the MLR process.Prepare and file FDA labeling and promotional material submissions and communicate dissemination dates to appropriate personnel. 10 Provide support and/or oversight for outsourced pharmacovigilance activities and file safety report submissions with the FDA or other authorities as necessary. 11 Collaborate with Scientific Affairs leadership and other team members regarding projects and perform other duties as assigned. 12 Complete and/or manage all responsibilities expected of a Regulatory Affairs Manager.
Reporting to this Position:
No direct reports
Travel:
Position may require up to 10% travel
Work Shift:
This position works days, but may include extended hours and weekend work when required
Knowledge, Skills and Abilities:
  • Excellent oral and written communication skills
  • Strong problem solving and critical thinking skills
  • Strong organizational skills and attention to detail
  • Strong familiarity with MSOffice
  • Working knowledge of cGMPs (current Good Manufacturing Practices) and FDA (Food & Drug Administration) pharmaceutical regulations
  • Strong command of internet search tools and techniques for research-related responsibilities
  • Good time management with demonstrated ability to manage multiple priorities simultaneously
  • Able to operate successfully in a team environment
  • Strong interpersonal and influencing skills to participate and/or lead (as needed) cross-functional teams, successfully challenging them to work collaboratively on solutions and meet project deadlines
Education and Experience:
  • B.S. degree in Biology, Chemistry, or Allied Health Sciences desired
  • M.S. degree in Pharmacy (or a related scientific field) or M.P.H. preferred
  • Minimum 6 years of prior experience working in the pharmaceutical industry or equivalent process-related industry.Less experience may be acceptable with a graduate degree
Physical Demands and Work Environment:
  • Ability to sit for extended periods at a desk
  • Occasional awkward positions (bending, kneeling, reaching, etc.) in the performance of the job
  • Ability to wear appropriate PPE (personal protective equipment) as required for exposure to pharmaceutical operations (e.g. respirators, over-gowning, gloves, steel toe shoes)
  • Good eyesight to tolerate extended viewing of computer screen.Able to read, interpret, and create business documents and communications
  • Good manual dexterity to operate computer, keyboards, and general office equipment
GENERAL INFORMATION:
The expectation for all employees is to support the company's mission, vision, culture and core values while adhering to all company policies.The above information is intended to describe the general nature and level of work being performed by individuals assigned to this position.It is not intended to be an exhaustive list of all duties, responsibilities, and skills required.The position may require other duties as assigned and can be changed at any time by the company.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, genetic information, sexual orientation, gender identity, national origin, disability or veteran status.

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