Senior Manager, Global Controlled Substance Audit Lead

Pfizer

. Set and manage high-complexity project objectives .

Posted 9/18/2026full-timeCollegeville • Kansas • United StatesSenior💰 $139,100 - $231,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing high-complexity projects, regulatory compliance, and talent development within a regulated environment. Proven ability to lead teams, influence senior management, and implement strategic initiatives while maintaining effective communication and interpersonal relationships.

Highest-signal resume keywords

Project ManagementRegulatory CompliancePeople ManagementRecords ManagementMicrosoft Office Suite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementRegulatory ComplianceRecords ManagementKey Performance IndicatorsAudit Management

Soft Skills

Interpersonal SkillsCommunication SkillsLeadership

Tools & Technologies

Microsoft Office Suite

Industry Keywords

Regulated EnvironmentTalent DevelopmentCompliance IssuesStrategic DirectionExternal Agency Relationships

About the role

Key responsibilities & impact

Set and manage high-complexity project objectives
Lead and allocate people, technology, and financial resources, including resources outside direct authority
Share knowledge across multiple functions and contribute to knowledge management processes
Champion and implement innovative ideas while taking appropriate risks
Assess talent needs, identify talent, and hold managers accountable for developing a diverse talent pipeline
Lead teams in implementing strategic direction and influence senior management decisions
Investigate and resolve compliance issues
Conduct audits and maintain ownership of the Regulatory change process
Develop relationships with external agencies
Leverage regulatory intelligence
Support inspections and audits
Develop key performance indicators for compliance and improvement initiatives
Periodically support site operations, inspections, audits, investigations, and time-sensitive regulatory matters

Requirements

What you’ll need

BA/BS with 6+ years of experience, or MBA/MS with 5+ years of experience, or PhD/JD with 1+ year of experience, or MD/DVM with any years of relevant experience
Proven ability to handle complex and global projects efficiently
Deep understanding of records management within a regulated environment
Proficiency in Microsoft Office Suite
Effective interpersonal and communication skills
Experience in people management
Relevant regulatory expertise and business acumen
Up to 30% travel
Must be authorized to be employed in the U.S. by any employer
Permanent work authorization in the United States required
U.S. work visa sponsorship is not available now or in the future

Benefits

Comp & perks

Global Performance Plan with a bonus target of 17.5% of base salary
Share-based long-term incentive program
401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Paid holidays
Paid personal days
Paid caregiver/parental leave
Paid medical leave
Medical, prescription drug, dental, and vision coverage
Relocation assistance may be available based on business needs and/or eligibility