More jobs:
Manager, Quality Operations Compliance
Job in
Waltham, Middlesex County, Massachusetts, 02154, USA
Listed on 2026-06-02
Listing for:
Viridian Therapeutics Inc.
Full Time
position Listed on 2026-06-02
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
Job Description & How to Apply Below
Reporting to the Director, Quality Assurance, the Quality Operations Compliance Manager is responsible for leading and maintaining the quality compliance framework supporting Viridian's commercial operations, with a strong focus on product complaint management, quality system performance, and operational governance. This role ensures alignment with cGMP, GxP, and global regulatory requirements through oversight of quality systems, performance metrics, inspection readiness, and external partner compliance.
The successful candidate will collaborate closely with internal cross-functional stakeholders and external CMOs/CDMOs to drive robust quality oversight and continuous improvement across the product lifecycle.
This role may be based in our Waltham, MA headquarters, which would be a hybrid role, or it can also be fully remote. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
Responsibilities (including but not limited to):
* Lead end-to-end product complaint management for clinical and commercial products, including intake, triage, investigation oversight, root cause analysis, CAPA development, trending, and timely closure in compliance with regulatory requirements
* Own complaint trending and signal detection activities, escalating adverse trends and potential patient or product quality risks
* Review and approve complaint investigations and CAPAs from external partners, ensuring regulatory and quality system compliance
* Own and maintain Quality Operations dashboards, ensuring tracking, trending, and reporting of key quality indicators (KQIs) and compliance metrics across the quality system
* Develop, maintain, and present Quality Management Review (QMR) metrics, providing clear visibility of quality system performance, risks, and improvement opportunities to senior management
* Ensure effective implementation and continuous improvement of core QMS processes, including deviations, change controls, CAPAs, risk management, and document control
* Lead Supplier Review Boards, including development and maintenance of CMO performance metrics, scorecards, and routine quality performance assessments
* Provide quality oversight of external manufacturing partners (CMOs/CDMOs), including review of deviations, CAPAs, and effectiveness checks related to supplied product
* Support internal audits, partner audits, and health authority inspections, serving as a subject matter contact for complaints and quality system performance
* Partner cross-functionally with Technical Operations, Supply Chain, Analytical Development, Regulatory Affairs, and Pharmacovigilance to ensure integrated handling of complaints, investigations, and regulatory commitments
* Author, review, and approve SOPs, work instructions, investigation summaries, complaint reports, and other quality documentation supporting clinical and commercial operations
* Requires a Bachelor's degree in a relevant STEM discipline with 5+ years of experience in quality management and CDMO oversight, or a Master's degree in a related field with 3+ years of experience in quality management and CDMO oversight
* Demonstrated experience leading product complaint management in a regulated pharmaceutical or biotechnology environment, including complaint trending and health authority reporting support
* Proven experience developing and maintaining quality dashboards, KQIs, and management review metrics to support data-driven decision making
* Strong…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×