Regulatory Affairs Manager
Newport Beach, California, United States
Evolus is a performance beauty company with a customer-centric approach focused on delivering breakthrough products. We are seeking an experienced and driven Regulatory Affairs Manager to join our Regulatory Team. This role demands technical depth and a high bar for quality. If you join our team, you will be working on some of the most exciting opportunities and challenges we face, with a team that values growth, recognition, and camaraderie. In this role, you will be challenged to drive the success of Evolus in an effort to build a brand like no other. Let’s talk about some of the key responsibilities of the role:
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- Responsible for the preparation, compilation, submission, and submission tracking of US, EU, UK, Australian, Canadian and global regulatory drug and biologic submissions for Evolus’ products.
- Responsible for maintaining relationships and working with external publishing vendors to ensure all submissions to Global Health Agencies are submitted per agreed timelines and with exceptional quality.
- Manage regulatory assessment and guidance on product compliance topics including change controls, deviations and GMP investigations.
- Responsible for providing regulatory support and guidance to cross-functional teams and key stakeholders.
- Assist in determining regulatory requirements for registration, approval, and maintenance of existing drug/biologics and potential new drug products in global markets.
- Establish clear priorities and bring key projects to completion on time, within budget and of significant impact to the growth of the business.
- Effectively communicate project needs and deliverables to R&D and upper management as needed.
- Other duties as assigned
- Bachelor’s degree (or 5+ years of experience in related field)
- Strong proven hands-on Regulatory Affairs experience (3+ years) and knowledge of regulatory submission and maintenance requirements for US and global filings (EU, UK, Canada, Australia, etc.) for drug/biologic products.
- Effective planning, organizational and task management skills
- Ability to balance multiple projects with tight deadlines
- Detail-oriented and goal-driven individual
- Excellent facilitation and creative problem-solving skills
- Excellent communication skills while simultaneously being able to work independently
- Demonstrated ability to prepare complex documents/submissions and presentations
- Knowledge of manufacturing processes associated with drugs and biologics.
- Experience in working with regulatory documentation systems and IT systems for regulatory document maintenance.
- Fully Remote Optional
- Office Location - Newport Beach (hybrid onsite Tuesday, Wednesday and Thursday) / Monday + Friday remote optional
- Position reports directly to Vice President, Regulatory Affairs-Drug
- Some travel may be required
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Job Profile
Regions
Countries
Hybrid onsite Tuesday to Thursday Remote Monday and Friday
Benefits/Perks401(k) match Bonuses Camaraderie Dental Equity options Life Insurance Medical Recognition Short Term Disability Vision Vision Benefits
Tasks- Assess product compliance
- Communicate project needs
- Maintain vendor relationships
- Prepare and submit regulatory filings
- Provide regulatory guidance
Communication Detail Orientation Document Preparation GMP IT systems Organizational Planning Problem-solving Project Management Regulatory Affairs Regulatory Submission
Experience5 years
Education TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9
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