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Pfizer

Pfizer

www.pfizer.com

4 Jobs

100,188 Employees

About the Company

We're celebrating over 175 years of daring scientific innovation--and we're not done yet. Let's outdo yesterday. Protect your health at PfizerForAll.com

For additional information on our guidelines, please visit http://www.pfizer.com/community-guidelines

Listed Jobs

Company background Company brand
Company Name
Pfizer
Job Title
VP, Cybersecurity Governance, Risk, and Compliance (GRC)
Job Description
**Job Title**: VP, Cybersecurity Governance, Risk, and Compliance **Role Summary** Lead enterprise cybersecurity governance, risk management, and compliance programs to safeguard digital assets, ensure regulatory compliance, and mitigate enterprise-wide risks across applications, vendor relationships, and operations. Develop and execute strategic initiatives aligned with organizational goals and global regulatory requirements. **Expectations** - Bachelor’s degree in cybersecurity, risk management, or related field with 15+ years’ experience. - Minimum 8 years of leadership managing enterprise GRC functions. - Proven expertise in cyber risk management, regulatory compliance, audit readiness, and GRC technologies. **Key Responsibilities** - Define and execute enterprise GRC strategy, aligning with organizational objectives and regulatory standards. - Oversee risk identification, assessment, and mitigation planning for cyber, data, and operational risks. - Manage audit and compliance activities for ISO 27001, SOC 2, PCI DSS, SOX, and GxP. - Own configuration, integration, and automation of GRC platforms (e.g., RSA Archer). - Establish cybersecurity policies, standards, and procedures; drive adoption across business and IT units. - Lead application security governance, embedding secure development lifecycle practices. - Develop and sustain programs for data protection, privacy regulations (GDPR, CCPA, HIPAA), and third-party risk management. - Spearhead business continuity/disaster recovery (BCP/DR) strategies to ensure operational resilience. - Provide executive-level reporting on risk posture, compliance, and program performance. - Foster cross-functional collaboration with IT, Legal, Privacy, and Audit to embed risk management practices. - Lead high-performing GRC teams, prioritizing mentorship, accountability, and continuous improvement. **Required Skills** - Deep knowledge of NIST CSF, ISO 27001, SOC 2, PCI DSS, and SOX frameworks. - Expertise in third-party risk management, including vendor assessments and mitigation. - Experience leading secure application governance and secure development lifecycle initiatives. - Strong communication skills to translate technical risks into business insights for executives. - Proficiency in GRC technologies (e.g., RSA Archer, DLP platforms, BCP/DR solutions preferred). **Required Education & Certifications** - Bachelor’s degree in cybersecurity, IT, or related field. - CISSP certification (required); CISM, CRISC, or CISA preferred.
New york, United states
On site
Senior
10-10-2025
Company background Company brand
Company Name
Pfizer
Job Title
Vice President, Marketing and Ecosystem Platforms and Engineering
Job Description
**Job Title:** Vice President, Marketing and Ecosystem Platforms and Engineering **Role Summary** Lead the strategic design, engineering, and delivery of global digital platforms supporting Pfizer’s Marketing, Medical, Legal, and Regulatory teams. Drive innovation in digital ecosystems, ensuring alignment with enterprise goals and technical excellence. **Expectations** - Translate business strategy into scalable, secure digital platforms. - Foster continuous improvement and agile delivery across high-performing teams. - Align platform innovation with long-term digital transformation. **Key Responsibilities** - Define and execute enterprise platform strategy for marketing and ecosystem technologies. - Oversee architecture and delivery of core platforms (Adobe, AWS, Salesforce Marketing CRM, CDP, AI tools). - Ensure security, compliance, and cloud cost optimization (FinOps). - Advise senior leadership on technology decisions and cross-enterprise initiatives. - Build and lead a global team of engineers and external partners. **Required Skills** - Expertise in cloud architecture (AWS), AI/ML, and platform engineering. - Technical leadership in Adobe suite, Salesforce CRM, CDP, and identity platforms. - Experience with Python-based automation and web/mobile ecosystems. - Strategic governance and vendor management for complex projects. - Cross-functional collaboration to integrate engineering with business needs. **Required Education & Certifications** - Bachelor’s degree in Computer Science, Engineering, or related field; advanced degree preferred. - Proven track record in enterprise software leadership (preferably in healthcare/Pharma). - Cloud certifications (e.g., AWS) and AI/ML frameworks a plus.
Memphis, United states
Hybrid
Senior
09-11-2025
Company background Company brand
Company Name
Pfizer
Job Title
Director, Drug Product Quality Assurance
Job Description
**Job Title** Director, Drug Product Quality Assurance **Role Summary** Lead the quality assurance strategy for drug product development and manufacturing within a Division or Global Business Unit. Responsible for ensuring compliance with GMP, regulatory requirements, and internal audit standards while driving continuous improvement, talent development, and cross‑functional collaboration. **Expactations** - Executive leadership in quality assurance, overseeing multiple high‑complexity projects. - Financial stewardship of QA/QC budgets and resource allocation. - Development and execution of quality programs, audits, and metrics. - Influence and mentor senior managers and staff across functional lines. **Key Responsibilities** - Define and execute strategic direction, performance metrics, and compliance roadmap for QA/QC. - Manage people, technology, and budgets, including resources beyond direct authority. - Lead internal assessment program: schedule audits, train auditors, maintain audit records. - Develop, implement, and continuously improve QA/QC systems, processes, and documentation. - Communicate quality performance and risk metrics to stakeholders. - Foster a culture of continuous improvement, acceptable risk‑taking, and knowledge sharing. - Mentor and develop senior managers, support succession planning, and promote diversity. - Oversee project portfolio, ensuring on‑time delivery and regulatory compliance. - Act as liaison with regulatory bodies, external auditors, and internal departments. **Required Skills** - Extensive people‑management and talent‑development experience. - Deep understanding of GMP, regulatory frameworks, and quality systems. - Strong strategic thinking, problem‑solving, and decision‑making. - Excellent written and verbal communication; interpersonal influence. - Ability to juggle multiple concurrent projects. - Proven track record of leading quality initiatives and driving continuous improvement. **Required Education & Certifications** - BA/BS with ≥8 years experience; MBA/MS with ≥7 years; PhD/JD with ≥5 years; MD/DVM with ≥4 years. - Preferable Master’s with pharmaceutical experience or relevant certifications in quality assurance (e.g., CQE, APQP, or Certified Quality Auditor).
Kalamazoo, United states
On site
Senior
20-11-2025
Company background Company brand
Company Name
Pfizer
Job Title
Quality Assurance Associate
Job Description
Job title: Quality Assurance Associate Role Summary: Execute and maintain Good Manufacturing Practice (GMP) records and documentation processes in a pharmaceutical setting, ensuring accuracy, traceability, and compliance with regulatory standards. Expectations: - Produce precise, compliant batch records and controlled documents. - Explore and log GMP records, facilitating retrieval and audit readiness. - Collaborate with cross‑functional teams to refine document control systems. - Support audits and inspections through timely record provisioning. - Drive continuous improvement in document and records management. Key Responsibilities - Follow established SOPs, work instructions, and templates for batch record issuance and reconciliation. - Process documents in an electronic Document Management System and maintain controlled document locations. - Log, catalog, file, and retrieve GMP records, both physical and electronic. - Scan, digitize, and verify records as true copies. - Participate in cross‑functional initiatives to update or upgrade systems related to GMP records. - Support GMP regulatory audits and inspections by ensuring accessible records. - Manage off‑site storage interactions and ensure compliant record submission. - Assist in reporting relevant metrics and contributing to project milestones. - Engage in continual improvement activities within Document Control and GMP Records management. Required Skills - Knowledge of current Good Manufacturing Practices (GxP). - Experience in pharmaceutical quality systems and document control. - Proficiency with electronic Document Management Systems. - Strong written and oral communication. - Teamwork and collaboration across departments. - Detail‑oriented with strong organizational skills. - Ability to multitask and manage time effectively. Required Education & Certifications - Bachelor’s degree in a relevant field (any experience) or Associate’s degree with ≥3 years of relevant experience, or high school diploma/equivalent with ≥6 years of relevant experience. - No specific certifications required, but familiarity with GMP, CAPA, and change control concepts is preferred.
Bothell, United states
On site
Junior
01-12-2025