Salary
💰 $120,800 - $201,400 per year
About the role
- Provide key support for SI/Bio related site quality technical operations activities and facility design across GTEL, Pharm Sci and Pfizer Global Supply sites
- Provide strategic and tactical leadership of cross-disciplinary teams to enable effective quality and compliance outcomes
- Lead commissioning, qualification & verification of new facilities and facility/utility changes, remediation activities and implementation of new technologies
- Direct and coach sites on standardized approaches to specific quality requirements for new facilities, facility changes, upgrades and systems
- Drive issue resolution and initiatives related to risk assessments, control strategy development, remediation activities and manufacturing innovations
- Liaise with Site Leadership Teams, Operating Unit Quality Operations Leads, GTEL Technical & Engineering, Regulatory, R&D and Drug Safety
- Support and lead SI/Bio platform to ensure consistent quality approaches for utilities, facility requirements, aseptic requirements, Next Gen innovations, lab of the future & predictive plants
- Partner with GTEL Process and Engineering Technology teams and support new product launches and tech transfers
- Provide quality oversight, leadership/approval of complex initiatives and facility designs, and develop site colleagues' understanding of policies, procedures and facility/utility guidance
- Provide subject matter expertise to drive simplified and standardized global and local processes for key technical disciplines
Requirements
- Bachelor’s degree with at least 6+ years of experience OR Master’s degree with more than 5+ years OR Ph.D. with 1+ years of experience
- Experience in Pharmaceutical manufacturing Facility role, technical or quality roles
- Strong knowledge of quality and compliance requirements, commissioning, qualification & verification
- Proven leadership skills and ability to achieve results through others
- Proficient in computer skills (e.g., Microsoft Office, ERP systems, MS Project)
- Relevant pharmaceutical experience (preferred)
- Experience working with complex organizations (preferred)
- Experience with Operational Excellence techniques (six sigma, etc.) (preferred)
- Excellent interpersonal, communication and coaching skills; ability to influence at all management levels
- Ability to drive change and positively influence others
- Leadership, integrity, team orientation, flexibility, creativity, strong analytical skills
- Experience in projects requiring collaborative approaches
- Experience of incident management processes through NTM, ESQRT, AQRT and BoH notification
- Permanent work authorization in the United States required