Manager, QMS Vendor Management & Supplier Notifications
About the position
Vaxcyte is seeking a Manager, QMS Vendor Management & Supplier Notifications to support the effective management of supplier-related quality activities within the Quality Management System (QMS). This role will be responsible for the intake, triage, and coordination of supplier notifications within Veeva QMS, ensuring timely impact assessments and appropriate follow-up actions. The individual will partner cross-functionally to assess risk, drive change controls, and maintain supplier compliance. This role will also contribute to vendor qualification activities, supplier management processes, and may support internal and external audit activities as needed.
Responsibilities
• Manage the end-to-end lifecycle of supplier notifications within Veeva QMS, including intake, triage, prioritization, and tracking.
• Perform initial assessments of supplier notifications to determine required actions and level of impact.
• Assign and coordinate impact assessments with cross-functional stakeholders (e.g., Quality, Regulatory, Manufacturing, Supply Chain).
• Ensure timely closure of supplier notifications in alignment with internal procedures and regulatory expectations.
• Maintain visibility of notification status, risks, and trends, escalating issues as appropriate.
• Facilitate and track impact assessments to evaluate potential effects on product quality, regulatory filings, and supply continuity.
• Coordinate and manage follow-up actions, including change controls, supplier communications, and documentation updates.
• Ensure actions are completed in a timely manner and in compliance with QMS requirements.
• Support risk-based decision making and documentation aligned with GxP expectations.
• Support vendor qualification and requalification activities, including risk assessments and documentation review.
• Maintain supplier records and ensure compliance with approved supplier lists and quality agreements.
• Partner with cross-functional teams to ensure suppliers meet Vaxcyte quality and compliance standards.
• Assist in maintaining supplier performance metrics and supporting supplier oversight activities.
• Participate in internal and external audits, including supplier audits, as needed.
• Support audit preparation activities and contribute to responses and CAPA development for audit observations.
• Assist in tracking and closure of audit-related actions.
Requirements
• BA or BS in a scientific or related field.
• Minimum of 5 years of experience in Quality Assurance, Supplier Quality, or Vendor Management within the biopharmaceutical, vaccine, or regulated industry. Other combinations of education and/or experience may be considered.
• Experience working within a Quality Management System (QMS), preferably Veeva QMS.
• Strong understanding of GxP regulations (GMP, GLP, GCP) and supplier quality requirements.
• Experience with supplier notifications, change control, and impact assessments preferred.
• Familiarity with vendor qualification and audit processes.
• Strong organizational and project management skills with the ability to manage multiple priorities.
• Excellent communication and cross-functional collaboration skills.
• Detail-oriented with strong problem-solving and risk assessment capabilities.
Nice-to-haves
• ASQ certification (CQA, CQE) or auditor certification preferred.
Benefits
• comprehensive benefits
• equity component
Vaxcyte is seeking a Manager, QMS Vendor Management & Supplier Notifications to support the effective management of supplier-related quality activities within the Quality Management System (QMS). This role will be responsible for the intake, triage, and coordination of supplier notifications within Veeva QMS, ensuring timely impact assessments and appropriate follow-up actions. The individual will partner cross-functionally to assess risk, drive change controls, and maintain supplier compliance. This role will also contribute to vendor qualification activities, supplier management processes, and may support internal and external audit activities as needed.
Responsibilities
• Manage the end-to-end lifecycle of supplier notifications within Veeva QMS, including intake, triage, prioritization, and tracking.
• Perform initial assessments of supplier notifications to determine required actions and level of impact.
• Assign and coordinate impact assessments with cross-functional stakeholders (e.g., Quality, Regulatory, Manufacturing, Supply Chain).
• Ensure timely closure of supplier notifications in alignment with internal procedures and regulatory expectations.
• Maintain visibility of notification status, risks, and trends, escalating issues as appropriate.
• Facilitate and track impact assessments to evaluate potential effects on product quality, regulatory filings, and supply continuity.
• Coordinate and manage follow-up actions, including change controls, supplier communications, and documentation updates.
• Ensure actions are completed in a timely manner and in compliance with QMS requirements.
• Support risk-based decision making and documentation aligned with GxP expectations.
• Support vendor qualification and requalification activities, including risk assessments and documentation review.
• Maintain supplier records and ensure compliance with approved supplier lists and quality agreements.
• Partner with cross-functional teams to ensure suppliers meet Vaxcyte quality and compliance standards.
• Assist in maintaining supplier performance metrics and supporting supplier oversight activities.
• Participate in internal and external audits, including supplier audits, as needed.
• Support audit preparation activities and contribute to responses and CAPA development for audit observations.
• Assist in tracking and closure of audit-related actions.
Requirements
• BA or BS in a scientific or related field.
• Minimum of 5 years of experience in Quality Assurance, Supplier Quality, or Vendor Management within the biopharmaceutical, vaccine, or regulated industry. Other combinations of education and/or experience may be considered.
• Experience working within a Quality Management System (QMS), preferably Veeva QMS.
• Strong understanding of GxP regulations (GMP, GLP, GCP) and supplier quality requirements.
• Experience with supplier notifications, change control, and impact assessments preferred.
• Familiarity with vendor qualification and audit processes.
• Strong organizational and project management skills with the ability to manage multiple priorities.
• Excellent communication and cross-functional collaboration skills.
• Detail-oriented with strong problem-solving and risk assessment capabilities.
Nice-to-haves
• ASQ certification (CQA, CQE) or auditor certification preferred.
Benefits
• comprehensive benefits
• equity component