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This posting covers multiple available positions. Role Summary   T he   Pfizer Patient Services (PPS)   Oncology   Business Unit   Support role   is responsible   for   the development of   patient services strategy ,   and   programmatic de s ign ,   for Pfizer’s   upcoming launch   products   in Oncology .   The   Director   is responsible for   establishing   the patient   services program   strategy for elements   across the   patient journey ,   including :     O verall program strategy   and design    C opay / affordability   support   H ub   support / operations   E xternal landscape monitoring   Program performance management   This role will   sit   within   the   PPS Oncology   BU   Strategy team   and will be accountable for ensuring   close   alignment with   Business Unit   and   Product...

Use Your Power for Purpose At Pfizer, every day is an opportunity to make a difference in patients' lives. Your contributions will directly impact patient care, as you work within a flexible, innovative, and customer-oriented culture rooted in science and risk-based compliance. By joining our team, you will help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy. What You Will Achieve The qualified candidate will deliver technical support for biotherapeutic products within Quality Control Product Technical Support group in Andover, MA. Applicants with proven organizational and communication abilities as well as comprehensive expertise and hands-on experience in pertinent analytical methodologies are strongly encouraged to apply. In this role, you will be responsible for managing and facilitating analytical activities throughout the lifecycles of...

Use Your Power for Purpose Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.  What You Will Achieve In this role, you will: Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications. Conduct rigorous sampling and statistical process control procedures to identify deviations from standards. Contribute to moderately complex projects, managing time effectively and developing short-term work plans. Independently assess Change Control activities for potential Quality and Operational Good Manufacturing Practices (cGMP) impacts. Investigate and document Quality Assurance deviations, escalating...