Senior Manager/Associate Director, Regulatory Operations

Company: Ocugen, Inc.
Location: Malvern
Posted on: November 2, 2025

Job Description:

Purpose The Senior Manager / Associate Director of Regulatory Operations will lead the planning, preparation, and execution of regulatory submissions to advance Ocugen’s biologics, cell, and gene therapy programs. This role provides strategic and operational leadership for global regulatory submission activities, ensuring compliance with electronic submission standards, and driving cross-functional alignment to meet critical regulatory milestones. Responsibilities Regulatory Submission Leadership Lead and oversee the preparation, formatting, publishing, and submission of regulatory documents for INDs, IMPDs, BLAs, MAAs, and amendments. Ensure submissions are fully compliant with FDA, EMA, Health Canada, and ICH electronic submission standards (eCTD). Provide oversight of regulatory publishing activities, including vendor management and internal coordination, to achieve on-time delivery. Establish and maintain submission trackers, dashboards, and metrics for organizational visibility and audit readiness. Regulatory Documentation & Compliance Provide high-level review of submission components (CMC, clinical, safety) for accuracy, consistency, and compliance. Drive best practices in document lifecycle management, including version control, archival, and audit preparedness. Serve as a subject matter expert, monitoring changes in regulatory requirements and proactively updating processes and systems. Cross-Functional & Strategic Coordination Partner with Regulatory Affairs, Clinical, CMC, Quality, and Medical Writing leadership to align submission strategies with development goals. Advise internal stakeholders on regulatory submission requirements, timelines, and risks. Lead collaboration with IT and external vendors to optimize submission platforms and tools, driving efficiency and compliance. Team & Vendor Leadership Provide mentorship and guidance to junior Regulatory Operations staff. Manage vendor relationships to ensure quality and timeliness of outsourced publishing activities. Contribute to department planning, resource allocation, and process improvement initiatives. Qualifications Bachelor’s degree in life sciences or related field required; advanced degree preferred. 7–10 years of experience in Regulatory Operations within the biotechnology or pharmaceutical industry, with increasing leadership responsibility. Proven expertise in global regulatory submission requirements, including FDA, EMA, Health Canada, and ICH guidelines. Demonstrated proficiency in eCTD publishing, electronic submission platforms, and regulatory information management systems (RIMS). Experience managing teams and/or vendors to deliver complex submissions on accelerated timelines. Strong organizational skills with the ability to prioritize and lead multiple projects simultaneously. Exceptional communication and influencing skills; able to effectively partner with cross-functional leaders and external stakeholders. Working Conditions This position operates in an office setting, in person. Job may additionally require incumbent to be available outside of these hours to handle priority business needs. Ocugen is an equal opportunity employer. In order to provide equal employment and advancement opportunities to all individuals, we make all of our employment decisions based upon merit, qualifications, abilities, and an individual’s conduct and performance. We will not make any of our decisions, and will not discriminate against any employee or applicant, on the basis of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including sexual orientation, gender identity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past, current or prospective service in the uniformed services, genetic information, or any other characteristic protected from discrimination under the law. Ocugen complies with applicable federal, state and local laws governing nondiscrimination in employment.

Keywords: Ocugen, Inc., Lower Merion , Senior Manager/Associate Director, Regulatory Operations, Science, Research & Development , Malvern, Pennsylvania