[Remote] Specialist, Regulatory Affairs - CMC - Remote

Note: The job is a remote job and is open to candidates in USA. Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings throughout every stage of life. The Specialist, Regulatory Affairs - CMC will be responsible for Regulatory Affairs activities for assigned commercial and investigational development products from preclinical candidate designation through product approval, including regulatory submissions.

Responsibilities

• Serves as regulatory CMC representative on project teams to ensure that development activities support and comply with the relevant regulatory requirements
• Reviews proposed CMC changes and assesses regulatory impact and filing requirements
• Supports the preparation, submission, and management of regulatory filings (INDs, CTAs, BLAs, etc.) to health authorities
• Collaborates on submission content with contributing authors across functional areas to achieve clarity and regulatory compliance (INDs, CTAs, BLAs/NDAs, meeting packages, responses, supplements, annual reports)
• Ensures timely preparation of organized and scientifically valid applications
• Contributes to the development of internal regulatory CMC guidance and SOPs
• Reviews/contributes to product development plans for assigned submissions/products
• Interacts with regulatory agencies on defined matters
• Responsible for executing regulatory documentation infrastructure, including paper and electronic submissions
• May be required to travel up to 15%

Skills

• Minimum of a Bachelor's degree in Chemistry, Biology, Pharmaceutical Science or related field
• Must be Proficient in MS Office Suite (Word, Excel, PowerPoint, Outlook)
• 0-2 years of experience in Regulatory Affairs
• Strong written and verbal communication, organizational, and people skills
• Demonstrate strong analytical, problem-solving skills, and attention to detail
• Ability to work cross-functionally and manage multiple projects simultaneously
• Regulatory Affairs Certification or equivalent training
• Experience in pharmaceutical Regulatory Affairs with a focus in drugs/biologics
• Experience in preparation, submission and lifecycle management of investigational/marketing applications in eCTD format
• Knowledge of US, EU, Health Canada, and ICH regulatory requirements
• Experience directly interfacing with regulatory authorities

Benefits

• Competitive Compensation including base salary and annual performance bonus.
• Flexible PTO, holidays, and parental leave.
• Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!

Company Overview

Company H1B Sponsorship