Director, RA-CMC PAC DM

Responsibilities

• Leads a global RA CMC PAC DM team who project manages marketed product variations including authoring and compilation of chemistry, manufacturing, and control (CMC) sections to ensure timely preparation of submission documents.
• Devises (or advises their team on) tactical strategies for executing post approval changes with complicated scenarios (e.g., complex dosage form or multiple operational changes, aggressive timelines).
• Provides leadership to PAC-DM staff to ensure consistency in the execution of post approval changes across all global programs.
• Provides direction and guidance to direct reports and their teams, as applicable, who exercise significant latitude and independence in their assignments.
• Effectively mentors staff to achieve business objectives and staff member personal growth. Reviews and provides feedback on RA training programs.
• Provides leadership to PAC-DM staff by communicating and providing guidance towards achieving department objectives. Identifies engagement needs and partners with stakeholders to implement action plans accordingly.
• Trains, develops and mentors individuals; includes formal supervisory responsibilities. Evaluates performance of and assists in career development planning for PAC-DM staff.
• Required Education: Bachelor's degree in pharmacy, biology, chemistry, pharmacology, engineering or related subject.
• Preferred Education: Relevant advanced degree preferred. Certification a plus.
• Required Experience: 10 years biopharmaceutical experience with 3-plus years demonstrated enterprise leadership. 5-plus years in RA or relevant exposure to RA activities.
• Preferred Experience: 10-plus years biopharmaceutical experience including 7-plus years in regulatory affairs, 2-plus years supervising employees.
• Prior experience in the preparation of CMC sections of regulatory dossiers including electronic submissions.
• Strong working knowledge of manufacturing unit operations and CTD structure.
• Strong oral and written communication skills.
• Strong understanding of the business/enterprise.
• Ability to work collaboratively with all levels and types of global personnel.
• **Equal Opportunity Employer Minorities/Women/Veterans/Disabled**
• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term incentive programs.
• AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
• US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
• US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
• https://www.abbvie.com/join-us/reasonable-accommodations.html

Benefits

Additional Information

The Director Regulatory Affairs for Chemistry, Manufacturing and Controls Post Approval Change Dossier Management (CMC PAC DM) combines scientific, regulatory and business knowledge with superior leadership skills to lead the PAC DM team responsible for ensuring RA-CMC post approval change objectives are met. Builds and maintains partnerships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Provides an environment for staff members to develop their careers and take their own leadership positions throughout AbbVie.

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