Pharmaceutical Regulatory Affairs Technician

Company: Actalent
Location: Westerville
Posted on: February 20, 2026

Job Description:

Job Description Job Description We are hiring for a Regulatory Affairs Technician role that will be focused on reviewing regulatory documentation to be submitted to the FDA and other regulatory bodies for review. This role is primarily a desk based job and will specifically focus on working with regulatory requirements around labeling pharmaceutical products. An ideal candidate for this role will have a Bachelors Degree in a Scientific field. This is an entry-level position and a great opportunity for someone who wants to be in the sciences without being in a laboratory environment. Job Description We are seeking a dedicated and detail-oriented Regulatory Affairs Technician to ensure that new and generic pharmaceutical products comply with established state and federal regulations. The role involves providing guidance for the submission of federal regulations, reviewing product labels and raw material information, and preparing electronic regulatory documents for submission to the FDA. Responsibilities Ensure compliance of pharmaceutical products with state and federal regulations. Provide guidance for the submission of federal regulatory documents. Review and analyze product labels and raw material information. Research and analyze industry-specific regulations in pharmaceutical manufacturing. Prepare electronic regulatory documents for FDA review and submission. Qualifications: Bachelor's degree in a scientific field. Comfortability with being in a desk based, non-laboratory role in the sciences. Job Type & Location This is a Permanent position based out of Columbus, OH. Pay and Benefits The pay range for this position is $22.00 - $22.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on Feb 27, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Keywords: Actalent, Hamilton , Pharmaceutical Regulatory Affairs Technician, Science, Research & Development , Westerville, Ohio