Senior Manager, Regulatory Affairs

Qualifications and Education Requirements

• Minimum Bachelor of Science or preferred advanced health care discipline degree (PharmD, PhD, Master of Science, etc.) or equivalent qualification.
• Minimum of 10 years in the pharmaceutical industry with at least 8 of those years in regulatory affairs.
• Combination of education and applicable job experience may be considered.
• Excellent organizational, interpersonal, verbal, and written communication skills, strong grammar, and proofreading/editing skills, and MS Office skills are required.
• Track record of successfully working with cross-functional teams, including external partners
• Ability to work independently with minimal supervision in a fast-paced deadline driven environment.
• Keen attention to detail.
• Ability to rapidly adapt to changing environment and circumstances that require flexibility, tolerance and a great sense of urgency while ensuring that all regulatory requirements are met.
• Ability to successfully communicate, negotiate and influence regulatory strategy to key stakeholders.

Principle Responsibilities

1. 1Represent Regulatory Affairs on assigned product and related project teams (both internal and external cross-functional teams)
2. 2Provide regulatory assessment of due diligence requests to support new business development activities.
3. 3Serve as primary interface with FDA and Health Canada for assigned products. Prepare and author portions of Health Authority meeting request and briefing documents.  Attend Health Authority meetings as assigned.
4. 4Drive regulatory strategies for drug product registration and for life-cycle management across North America.
5. 5Manage regulatory filings including IND, NDA, ANDA, NDS, DMF for a variety of dosage forms including solid oral, parenteral, liquids, topicals, inhalation and nasal, and drug/device combination drug products. Respond to FDA or Health Canada Requests for Information.
6. 6Manage operational aspects of preparing compliant submissions to regulatory agencies.
7. 7Establish and manage timelines associated with regulatory submissions.
8. 8Manage archive of regulatory submissions, regulatory correspondence and associated logs and tracking mechanisms as per Azurity SOPs.
9. 9Provide regulatory guidance on requirements for post-approval/life-cycle changes, as required, for assigned commercial products including change control assessments.
10. 10Provide regulatory support for Senior Leadership Team (SLT) and Executive Leadership Team (ELT) meetings and presentations.
11. 11Monitor evolving, region-specific regulations and proactively provide strategic guidance to cross-functional teams to ensure compliance.
12. 12Assist in preparing budgets and reviewing invoices on assigned projects and relevant product/filing fees, as needed.
13. 13Participate in various activities of setting goals, tracking deliverables and process improvements within the regulatory department.