
201 - 500 employees
💊 Pharmaceuticals
🤝 B2B
Pharmaceuticals • B2B
Padagis LLC is a pharmaceutical manufacturer focused on expanding access to high-quality, affordable topical and other non-oral medications. The company develops and produces a broad portfolio of prescription and over-the-counter extended topical products—including creams, ointments, gels, foams, sprays, patches, nasal treatments, and suppositories—and specializes in Paragraph IV generic products that navigate branded patent complexities. Padagis also pursues research and development, strategic partnerships, product acquisitions, and contract manufacturing to support healthcare providers, distributors, and patients.
🕒 April 2
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201 - 500 employees
💊 Pharmaceuticals
🤝 B2B
Pharmaceuticals • B2B
Padagis LLC is a pharmaceutical manufacturer focused on expanding access to high-quality, affordable topical and other non-oral medications. The company develops and produces a broad portfolio of prescription and over-the-counter extended topical products—including creams, ointments, gels, foams, sprays, patches, nasal treatments, and suppositories—and specializes in Paragraph IV generic products that navigate branded patent complexities. Padagis also pursues research and development, strategic partnerships, product acquisitions, and contract manufacturing to support healthcare providers, distributors, and patients.
• Oversee regulatory strategies, submissions, and writing for pharmaceutical products targeted for the U.S. market • Work cross-functionally with internal teams and external stakeholders to ensure regulatory compliance • Provide consultation on regulatory aspects during the development phase • Ensure all activities are planned and executed for a successful submission • Guide products through the development pipeline and secure FDA approval
• Advanced degree in life sciences, pharmacy, or a related field • 7–10+ years of experience in Regulatory Affairs within the pharmaceutical or biotechnology industry • Proven track record of leading and successfully managing ANDA, IND, NDA, submissions and approvals with the FDA • Experience in regulatory strategy planning for generic drugs and combination products • Strong knowledge of FDA regulations and guidelines, including regulatory requirements for preclinical, clinical, and CMC submissions • Exceptional project management skills with the ability to manage multiple priorities and deadlines • Strong analytical and problem-solving skills with a proactive and solutions-oriented mindset • Excellent communication and interpersonal skills for effective collaboration with internal teams, external partners, and regulatory agencies.
• Remote work options • Professional development opportunities
Apply Now🕒 April 2
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