Senior Associate, Regulatory Affairs

About the role

Employment Type: Full Time

Location: Hybrid (Cincinnati, Ohio) - Location Address: 4545 Creek Rd Blue Ash, OH 45242

• Responsible for managing, planning, preparation, and delivery of documents both electronic- and paper-based in support of assigned. global regulatory product registrations, renewals, tenders/customs, etc.
• Coordinate the preparation and submission of medical device applications by providing regulatory information and documents and following up closely on queries from inspection through approval.
• Prepare and/or review letters of authorization, cover letters for registration certificates, declarations, power of attorney, and other regulatory documentation to ensure accuracy, appropriateness, and consistency of documents intended for various global regulatory submissions.
• Submit and manage applications for the US FDA Certificates to Foreign Government (CFGs).
• Maintain various tracking tools to ensure up-to-date information and traceability of all regulatory data/documentation.
• Perform and/or coordinate legalization, notarization, and apostille of regulatory documents
• Ensure compliance with current good documentation practices, including but not limited to proofreading, formatting, indexing and recordkeeping.
• Assist all regions in answering inquiries and providing required documents and information utilizing various search tools and systems.
• Perform document filing and retrieval functions as directed and per company's policies and procedures.
• Effectively communicate with internal and external teams and/or clients as to the status of deliverables, to ensure timely and satisfactory completion of tasks and expectations.
• Communicate with the project teams on a regular basis regarding regulatory updates.
• Provide support to internal and external teams to address various technical inquiries and provide requested data/information
• Participate in group meetings and provide tactical approaches to addressing issues of basic complexity
• Perform other tasks as assigned.

Experience/Skills

• Bachelor's degree (Life Sciences or a regulatory related field preferred)
• Minimum of 1 year of hands-on experience in medical device regulatory affairs, or at least 3 years of combined regulatory affairs and related experience.
• Basic knowledge of US FDA QSR, ISO 13485, EU MDD/MDR.
• Knowledge of global medical devices registration process is a plus
• Proficient in Microsoft Office (e.g., Word, Excel, PowerPoint)
• Have a good understanding of current Good Documentation Practices in a regulatory environment.
• Self-starter with the ability to work in a team environment and on projects of diverse scope where analysis of a situation or data requires evaluation of various factors with minimal supervision.
• Excellent organizational skills with strong attention to detail, effective planning, and the ability to multitask efficiently
• Must possess excellent written and verbal communication skills.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.