The "Senior Issue Lead, Inspections" will be accountable to drive GCP quality in withstanding regulatory scrutiny, operational data and documentation. Major areas of focus will include:

• Directing Inspection readiness and providing inspection support for GCP sponsor inspection activities
• CAPA management

Inspection Coordination

This individual may be assigned additional focus areas in inspection coordination, including inspection responsibilities around:

• Directing asset/study team colleagues within CS&O/Clinical to ensure successful inspection and audit outcomes
• Leading key activities in the inspection control room as required
• Communicating audit and inspection progress and needs to CS&O/Clinical stakeholders
• Serving as the point of contact for Regulatory Quality Assurance related to inspection CAPA management

Quality Compliance Assessment

Plan, lead and report out on Quality and Compliance Assessments related to CS&O processes.

Training and Technology

This individual will also be required to mentor and train Issue Leads to ensure the individuals coordinating inspection readiness, and those providing inspection support are qualified to assess and support inspections.

BS – 10+ years or equivalent MS/MBA – 9+ years or equivalent

Previous Experience:

• BS – 10+ years or equivalent MS/MBA – 9+ years or equivalent

• Minimum of 5 years of pharmaceutical experience with solid experience in data management, operational aspects, GCP Quality, GxP Quality, and/or regulatory quality
• Regulatory inspection experience
• Process and system management experience
• Detailed knowledge of clinical trial processes and relationships required
• Knowledge of GCP requirements and applicable SOPs and regulations
• Project management, administrative, and technical capabilities are required, as well as effective verbal and written communication skills
• Strong background in continuous improvement methodology (i.e., Lean Six Sigma) preferred

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

#LI-PFE

The annual base salary for this position ranges from $149,200.00 to $248,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Quality Assurance and Control