Senior Manager, Quality Systems

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Full Time Management Plymouth Meeting Office, Plymouth Meeting, PA, US

Harmony Biosciences is recruiting for a Senior Manager, Quality Systems in our Plymouth Meeting office
. In this role, you will provide day-to-day operational support for GxP Quality Systems in accordance with applicable ICH and FDA regulations and guidelines. The role is responsible for the daily administration and maintenance of Quality Events, controlled documents, training processes, workflows, SOP revisions, and Quality metrics to support compliant and inspection-ready Quality Systems. The position works directly with process owners and business functions to maintain accurate records, troubleshoot system and workflow issues, monitor assigned activities, facilitate timely completion and escalation, and support consistent execution and continuous improvement of established Quality processes.

Responsibilities include but are not limited to:

• Manage and maintain a compliant state of the electronic Quality Systems, including but not limited to Document Management, Training, Change Control, Deviations, and CAPA.
• Provide day-to-day support for Quality Events, including Change Controls, Deviations, CAPAs, and Continuous Improvement records, from initiation through review, approval, implementation, and closure.
• Monitor Quality Event workflows, record quality, aging, and due dates; identify bottlenecks, facilitate timely escalation, and support sustainable process improvements.
• Draft, revise, route, and periodically review SOPs, work instructions, forms, and other controlled documents to maintain alignment with current processes and applicable GxP requirements.
• Ensure harmonization across GxP domains (GMP/GLP/GCP) and alignment with applicable regulations/standards.
• Provide operational support to Technical Operations, Regulatory Affairs, Clinical Operations, and Medical Affairs by troubleshooting Veeva Vault and other GxP system issues, coordinating issue resolution, assisting users, and supporting approved workflow improvements.
• Administer the GxP training program and related Quality processes, including Veeva Vault Training, role-based curricula, training assignments, periodic review activities, and maintenance of inspection‑ready training records.
• Ensure that systems and business processes meet organizational business needs and regulatory requirements.
• Provide day-to-day administration and user support for document lifecycle activities within Veeva Vault Quality Docs, including document creation, review and approval workflows, periodic reviews, and archival activities.
• Develop, compile, analyze, and maintain Quality System metrics and trends, including cycle times, overdue items, training compliance, audit outcomes, CAPA effectiveness results, and open improvement actions; prepare and present assigned materials for Quality Management Review to support performance monitoring, risk escalation, and continuous improvement.
• Partner with process owners and cross‑functional stakeholders to clarify Quality System requirements, resolve workflow issues, reinforce procedural compliance, and promote consistent use of the eQMS.
• Provide oversight and support for additional GxP‑regulated systems, as needed. Perform other duties as assigned.

Qualifications:

• Bachelor’s degree in life sciences, engineering, pharmacy, or a related discipline required; advanced degree preferred
• 7+ years within GMP Quality Assurance, Quality Systems, technical operations quality, or manufacturing quality required specifically within the pharmaceutical or biotechnology industry
• Demonstrate…