Senior Quality Operations Specialist

Ascend Advanced Therapies is seeking a Senior Quality Specialist, Quality Operations to provide end-to-end Quality Assurance support for the manufacture and release of gene therapies, oncolytics, vaccines, immunotherapies, and other biological products in a GMP-regulated environment. This role partners closely with Manufacturing, Quality Control, and cross-functional teams to ensure compliance with FDA, EU, and ICH regulatory requirements while supporting product disposition, batch record review, investigations, CAPAs, change controls, audits, and continuous improvement initiatives.

The ideal candidate brings strong GMP Quality experience within biologics, cell therapy, or gene therapy manufacturing and possesses the ability to apply regulatory requirements to complex operational situations while promoting a culture of quality throughout the organization.

Provide end-to-end Quality support for the manufacture of mid-phase through Commercial gene therapies, oncolytics, vaccines, immunotherapies, or other biological products under the regulatory purview of current Good Manufacturing Practices (21 CFR Parts 210/211, 600, and 610); to include, but not limited to, the following:

o Review and approve master batch records, material specifications, quality control test methods/validations, raw material inspection and release packets, environmental monitoring data, and any other documentation associated with the development, execution, and review/approval of manufactures for product release.

o QA on the Floor

o Room Release activities

o Drafts and/or approves Certificates of Analysis, Certificate of Compliance, and any other certificates issued to Clients in support of product disposition and release.

o Acts as QA representative in Client meetings; providing sound Quality perspectives, citing the appropriate regulations, standards, or guidance to resolve potential issues.

o Acceptance Quality Limit (AQL) inspections

o Review and approve master batch records, material specifications, quality control test methods/validations, raw material inspection and release packets, environmental monitoring data, and any other documentation associated with the development, execution, and review/approval of manufactures for product release.

o QA on the Floor

o Room Release activities

o Drafts and/or approves Certificates of Analysis, Certificate of Compliance, and any other certificates issued to Clients in support of product disposition and release.

o Acts as QA representative in Client meetings; providing sound Quality perspectives, citing the appropriate regulations, standards, or guidance to resolve potential issues.

o Acceptance Quality Limit (AQL) inspections

• Write, review, and revise Standard Operating Procedures (SOPs)
• Provide QA oversight to ensure adherence to procedures, while also increasing compliance awareness and promoting a culture of quality throughout the company through strong collaborations with the cross-functional teams.
• Readily identify gaps in compliance during conversations and can devise an equitable solution that resolves the issue(s) and ensures regulatory compliance.
• Provide training in GxP regulations, best practices, and internal requirements
• Provide direct support in investigating complex issues and non-conformances – is able to use critical thinking to establish investigation plans and effective, data-driven discussions in evidence of root causes.
• Be proactive in forecasting upcoming tasks and is highly communicative with Management and other departments in establishing business priorities.
• Establish and implement effective CAPA and Change Control plans
• Performs internal and external (i.e. supplier/sub-contractor) audits.
• Assist with the analysis of trends and metrics to recommend and implement continuous quality improvements.
• Interface with contract testing organizations and alliance partners to resolve quality-related issues with minimal supervision
• Host Client audits and/or regulatory inspections.
• Other duties as assigned.

• Minimum of BS in Life Science or equivalent years of education and/or years of experience (i.e. Associate's Degree and minimum 5 years in a regulated pharmaceutical environment)
• A minimum of 5-7 years’ experience in a technical or administrative field related to the industry or equivalent in a GMP (biologics) environment is required.
• 5+ years of experience in biologics, cell therapy or gene therapy manufacturing Quality.

• Strong foundational…