Quality Assurance Manager - GMP

Integrated Resources, Inc ( IRI ); New Haven (CT); On-site; USD 95,000 - 150,000; Full time

Job summary

Integrated Resources, Inc ( IRI ) is seeking an experienced QA professional to guide clinical finished product release, deviations, and supplier quality within a regulated environment. You will lead investigations, CAPA tracking, data analysis, and risk assessments to ensure ongoing GxP compliance and robust quality systems.

The role emphasizes data-driven reporting, change control, and documentation reviews across internal and external stakeholders, supporting audits and continual process

Qualifications

• Bachelor's degree in science/engineering or related field with 8+ years QA/regulatory experience.
• Experience with quality processes across multiple areas in a regulated environment.
• Experience guiding clinical supply chain managers on compliance concepts.
• Experience troubleshooting across quality areas.

Responsibilities

• Guide core processes for clinical finished product release and distribution.
• Review investigations and track CAPA implementation to establish root causes.
• Lead quality agreement negotiations and supplier risk evaluations for packaging and labeling CMOs.
• Provide guidance on GxP and regulatory guidelines at the site.
• Support inspection readiness during internal audits and agency inspections.
• Conduct data analysis and develop reports on quality metrics and KPIs.

Skills

Quality Assurance

GxP Knowledge

Root Cause Analysis

Data Analysis

Education

Bachelor's degree in science/engineering

Tools

Veeva Vault

Power BI

Smartsheet

Copilot

Job description

Guide the execution of core processes related to clinical finished product release and distribution, including managing deviations, complaints, and supplier quality. Ensure timely data entry and documentation review and approval. Lead and approve investigations to establish root causes, track CAPA implementation, and approve investigation reports. Provide guidance on GxP, coordinate quality agreement review, change management and actively engage in process improvements and risk assessments. Conduct data analysis, develop reports on quality metrics and key performance indicators, and support overall planning for change management and guidance for internal and external stakeholders.

Typical Accountabilities

• Guide execution of core processes applicable to clinical finished product release and distribution.
• Guide timely data entry and documentation related to own quality area.
• Review and approve investigations to ensure root cause is established and relevant CAPAs are in place, and track implementation.
• Lead quality agreement negations and suppliers risk management evaluations for packaging and labeling CMOs
• Conduct / guide ongoing reviews and approvals of documentation as applicable.
• Provide advice on GxP within the site, with reference to guidelines and regulations.
• Actively engage in change management and process improvements and risk assessments, such as benchmarking internal and external quality assurance practices to identify innovative efficient and effective practices.
• Conduct data analysis and development of reports and insights on quality metrics and key performance indicators, using digital tools and processes.
• Support inspection readiness during internal audit and agency inspections.

Qualifications and Skills

Essential: High school education with significant experience or bachelor’s degree in science/engineering field such as Pharmacy, Biology, or Chemistry with some experience; Experience with quality processes across multiple areas; Experience interpreting and guiding clinical supply chain managers around principles and concepts of compliance management within a regulated environment; Experience troubleshooting issues across quality areas;

Minimum Experience: 8+ years

Desirable: Experience implementing newer digital tools (e.g. Power BI I think we wrote should be like "Power BI, Smartsheet, Copilot") and technologies related to QA reporting, documentation, and analysis. Must have Veeva Vault experience as a quality approver.