Manager, Quality Assurance, External Manufacturing

Manager, Quality Assurance, External Manufacturing Vaxcyte - 5.0 San Carlos, CA Job Details $151,000 - $176,000 a year 2 hours ago Qualifications Quality control corrective actions Document review (document control) Management Pharmaceutical regulatory compliance Corrective and preventive actions (CAPA) GMP ICH guidelines Bachelor's degree Quality control documentation Task prioritization Decision making Performance Improvement (PI) Risk management Batch records Root cause analysis Manufacturing company experience Cross-functional communication FDA regulations Full Job Description Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values:

RETHINK CONVENTION

We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.

AIM HIGH

We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.

LEAD WITH HEART

Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.

MODEL EXCELLENCE

The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.

Summary:

The Manager, Quality Assurance, External Manufacturing is responsible for overseeing quality activities at contract manufacturing organizations (CMOs), ensuring compliance with cGMP standards, and driving performance through KPIs and continuous improvement initiatives. This role leads batch disposition, reviews critical GMP documentation, supports PPQ activities, and collaborates cross-functionally to resolve complex manufacturing and quality issues. The position requires strong expertise in pharmaceutical quality systems, regulatory requirements, and risk management, along with leadership, problem-solving, and communication skills to support both clinical and commercial operations.

Essential Functions:

Provide Quality Assurance oversight of Contract Manufacturing Organizations (CMOs). Develop and report metrics and key performance indicators (KPIs) to evaluate CMO performance. Represent Quality Assurance at internal cross-functional meetings and Joint Project Team meetings. Lead polysaccharide batch disposition activities, including review of executed batch records, environmental monitoring data, and quality control results. Review and approve GMP documentation, including master batch records, deviations, risk assessments, change controls, and CAPAs. Drive resolution of quality performance issues in collaboration with contract manufacturers. Support Process Performance Qualification (PPQ) activities. Develop, implement, and maintain quality procedures, policies, and standards. Collaborate with key stakeholders to develop solutions to complex manufacturing and quality issues. Participate in compliance audits and regulatory inspections, as required. Promote a strong quality mindset and a culture of quality excellence across all activities.

Requirements:

Bachelor's degree in chemistry, Biology, Pharmacy, Engineering, or a related scientific discipline. Minimum 5 years of experience in managing CMO quality, and quality systems management within the pharmaceutical, biotechnology, or life sciences industry. Other combinations of education and experience may be considered. Experience in batch record review, deviations and Out of Specification (OOS) investigations. Thorough knowledge of c

GMP, ICH

guidelines, FDA/EMA, Swiss medic regulations, and international pharmaceutical quality standards. Experience applying Quality Risk Management principles. Experience supporting both clinical and commercial products preferred. Strong leadership, management, and process improvement skills. Excellent organizational skills with strong attention to detail. In-depth understanding of biologics manufacturing operations. Proven ability to prioritize multiple assignments in a fast-paced, changing environment. Strong problem-solving abilities, including managing complex investigations and root cause analyses. Excellent written and verbal communication skills, with the ability to clearly present quality topics and risk-based decisions to cross-functional teams.

Reports to:

Director, Quality Assurance Location:

Hybrid;

San Carlos, CA Compensation:

The compensation package will be competitive and includes comprehensive benefits and an equity component.

Salary Range:

$151,000 - $176,000 (SF Bay Area). Salary ranges for non-California locations may vary. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.