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Sr Manager, QA Operations

Job in Canton, Norfolk County, Massachusetts, 02021, USA
Listing for: Emergent Biosolutions
Full Time position
Listed on 2026-08-05
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Engineering, Quality Control - QC Analysts/Managers
Job Description & How to Apply Below

Sr Manager, QA Operations

Location:

Canton, MA, US, 02021 Preparedness today, safer tomorrow. Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.

JOB SUMMARY

The Senior Manager, Quality Assurance Operations provides senior leadership and oversight of GMP Quality Assurance Operations at a vaccine Drug Substance manufacturing site, ensuring compliant execution of manufacturing activities and effective implementation of site quality systems in alignment with Site Quality Management expectations and global Quality standards. This role is accountable for real time QA oversight of manufacturing operations, lifecycle management of deviations, CAPAs, change controls, validation activities, and risk management, while operating as a key Quality decision-maker independent of Production, consistent with CGMP requirements.

The position partners closely with QA Compliance and Supplier Quality, Quality Control, and Site Quality Management to ensure effective inspection readiness, audit support, risk escalation, and Quality Management Review (QMR) execution. The Sr. Manager supports internal and external projects, including technical transfers, supplier and partner interactions, and network initiatives, and is expected to cross train within the Quality Unit to ensure continuity of critical quality responsibilities.

This role directly contributes to sustaining a state of control, regulatory confidence, and a strong quality culture across site operations.

ESSENTIAL FUNCTIONS

Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.

Quality Operations Oversight

Provide senior QA oversight for GMP manufacturing operations, ensuring controls are implemented and executed in accordance with approved procedures and regulatory requirements. Maintain robust QA presence on the floor, supporting real time decision making, logbook review, batch documentation review, and issue resolution. Ensure Quality remains independent of production while enabling compliant execution.

Quality Systems Execution

Lead and oversee Deviations, CAPAs, Change Controls, Effectiveness Checks, and other site quality systems in accordance with SOP
040945 and global procedures. Ensure timely, high quality investigations using sound root cause analysis and risk-based decision making. Review and approve complex investigations, including manufacturing deviations, OOS/OOT events, and excursions.

Risk Management & State of Control

Apply Quality Risk Management (ICH Q9) principles to assess, escalate, and mitigate quality and compliance risks. Support site and corporate Quality Risk assessments and ensure alignment with Site Quality Management expectations. Identify adverse trends and partner with QA Compliance to ensure appropriate escalation to senior management.

Validation & Lifecycle Oversight

Provide QA oversight and approval for qualification and validation protocols, reports, and deviations for facilities, utilities, equipment, processes, QC methods, and computerized systems. Ensure validation activities align with regulatory expectations and site control strategy.

Inspection Readiness & Audit Support

Support internal audits and regulatory inspections by ensuring QA Operations processes, records, and personnel are inspection ready. Participate as a Subject Matter Expert during regulatory inspections and audits, supporting responses and remediation activities in partnership with QA Compliance. Ensure operational readiness for FDA (CBER), global health authorities, and partner audits.

Quality Metrics & Management Review

Develop, trend, and present Key Performance Indicators (KPIs) supporting Quality Management Review (QMR). Provide operational quality insights to support assessment of process performance, product quality trends, and state of control. Communicate quality performance to site and corporate Quality leadership.

People Leadership & Organizational Resilience

Lead, coach, and develop QA Operations personnel, ensuring proper training, qualification, and performance management. Promote cross-training within the Quality Unit to support continuity of quality responsibilities. Foster a culture of accountability, engagement, and continuous improvement.

Projects, Technology Transfer & Partnerships

Provide QA Operations leadership for technology transfer activities, lifecycle changes, and introduction of new or modified processes. Support internal and external partnerships by ensuring Quality requirements are integrated into execution and risk is appropriately managed. Collaborate with Supplier Quality and Compliance functions to ensure operational impacts from supplier or partner activities are properly assessed.

MINIMUM EDUCATION, EXPERIENCE, SKILLS

Due to the nature of this role and our manufacturing environment,…

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