Quality & Compliance Manager
Listed on 2026-01-25
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Quality Assurance - QA/QC
Quality Engineering, Quality Control / Manager, Regulatory Compliance Specialist, QA Specialist / Manager
Job Information
Job Title: Quality & Compliance Manager
Job Type: Full-time
Job Category: Professional
Department/Division: Quality/Operations
Created Date: 12/17/2025
The Quality & Compliance Manager will lead the development, management, and execution of the supplier quality management, internal audit & inspection readiness, and CAPA programs s role is responsible for supplier quality management of suppliers that provide raw materials, drug products, and GMP services to GSMS; the GSMS internal audit and inspection readiness program; and the GSMS CAPA prograom. This role oversees supplier qualification & performance, external & internal audit strategy, compliance with FDA regulations, and CAPA monitoring & effectiveness.
GeneralDuties and Responsibilities
- Responsible for the development and execution of the supplier quality management program and processes for GMP suppliers.
- Manage the quality of drug product, raw material, and GMP service suppliers to ensure GSMS and FDA requirements are met
- Qualify new suppliers per GSMS policies and procedures.
- Negotiate, approve and manage quality agreements between GSMS and suppliers
- Participate on a cross functional supplier management team with colleagues from Supply Chain, Purchasing, and Commercial Operations to assess, communicate, and manage supplier performance via scorecards and business meetings
- Develop and maintain supplier risk ranking including evaluating internal and supplier Preventive Controls
- Oversee the Supplier Change Notification (SCN) process, ensuring GSMS is notified of supplier changes and GSMS processes & procedures are thoroughly assessed and updated as required.
- Work collaboratively with suppliers and GSMS Quality teams on Supplier Corrective Action Request (SCAR) process, ensuring effective corrective actions are being taken by suppliers.
- Develop and maintain a current and accurate database of supplier quality management information such as Supplier History File, Approved Vendor List (AVL), risk analysis results, supplier performance, etc.
- Develop and manage GSMS external and internal audit programs.
- Oversee and conduct external and internal audits, ensuring any improvements or corrective actions are addressed to GSMS’s satisfaction.
- Manage GSMS CAPA program. Lead CAPA meetings and monitor timeliness & effectiveness of correction actions.
- Helps drive a culture of continuous improvement.
- Assist with leading regulatory and 3rd party inspections and audits, including pre-inspection readiness, inspection execution, and post inspection responses.
- Performs other quality and compliance-related duties as assigned.
Received:
Directives from Director, Quality & Regulatory Compliance. Given: N/A.
Standard office equipment, computers, safety glasses, cap, booties, gloves, as required.
Physical/Cognitive Requirements- Strong knowledge of FDA GMP regulations, practices and trends.
- Working knowledge of pharmaceutical processing and manufacturing processes.
- Strong communication skills at all levels, both written and verbal; both individually and in a group setting.
- Strong leadership, negotiation and influencing skills
- Strong skills in analytical thinking and problem solving.
- Proficiency in audit planning, execution, and reporting.
- Ability to translate complex data into actionable information
- Ability to evaluate complex compliance issues and concerns
- Ability to perform multiple tasks and ability to effectively manage conflict.
- Ability to work in teams to obtain results.
- Good decision-making skills. Ability to make decisions with limited information.
- Proactively identify issues and take action.
- Effectively manage change and comfortable changing direction and acting without complete information.
- Good organizational and prioritization skills.
- May be required to work longer than the typical 8-hour work day.
- Sedentary position that may requires pro-longed long periods of desk work.
- Requires light physical duties in keeping work areas clean and organized. Regularly required to walk the production and warehouse areas.
- Required working knowledge of basic Microsoft Office applications.
- Working knowledge of data analysis software and reporting.
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