More jobs:
Quality Assurance Associate III Scientific
Job in
Framingham, Middlesex County, Massachusetts, 01701, USA
Listed on 2026-06-04
Listing for:
Adecco US, Inc.
Full Time
position Listed on 2026-06-04
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist, Quality Control / Manager, QA Specialist / Manager
Job Description & How to Apply Below
* ** Quality Assurance Associate III - Third Party Management (Supplier Quality / GMP)*
* ** Fully Onsite | Temp Role (6 Months) | Free Parking | Framingham, MA*
* ** Pay** : 50-62/hr depending on education and relevant experience level
** Position Summary*
* The Quality Assurance Associate III - Third Party Management Specialist is responsible for overseeing supplier and external partner quality operations within a GMP-regulated biotech manufacturing environment. This role focuses on supplier quality management, material compliance, and third-party risk oversight, ensuring compliance with global regulatory standards and internal quality systems.
The position supports supplier change notifications, quality agreement management, and investigations related to material or supplier-related quality events, working closely with QC, Manufacturing, Facilities, and external vendors.
** Key Responsibilities*
* ** Third Party & Supplier Quality Management*
* + Manage third-party quality operations for external suppliers supporting the Bio Campus manufacturing site
+ Lead Supplier Change Notification (SCN) processes and ensure timely assessment and documentation of supplier changes
+ Conduct and support investigations related to supplier quality events, material defects, and compliance issues
+ Ensure alignment of supplier activities with quality agreements and regulatory requirements
** Quality Systems & Compliance Oversight*
* + Support development, review, and periodic updates of Quality Agreements with external partners
+ Ensure compliance with GMP and global regulatory standards (US, EU, Canada, Japan, Australia)
+ Maintain documentation within Quality Management Systems (QMS) such as Veeva
+ Support audits, inspections, and compliance reviews related to supplier quality programs
** Cross-Functional Collaboration*
* + Collaborate with QC, Manufacturing, Facilities, and Supply Chain teams to resolve supplier-related quality issues
+ Communicate directly with external suppliers to investigate deviations and material compliance concerns
+ Support resolution of quality events impacting single-use systems and raw materials
+ Participate in cross-functional discussions regarding supplier performance and compliance risk
** Documentation & Continuous Improvement*
* + Maintain accurate records of supplier quality activities, investigations, and change notifications
+ Support continuous improvement initiatives within third-party quality systems
+ Contribute to process optimization and enhancement of supplier oversight programs
+ Ensure timely escalation of compliance risks and material issues
** Required Qualifications*
* + Bachelor's degree required with 6+ years of relevant experience in Quality, Supplier Quality, or GMP operations
+ Experience in pharmaceutical or biotech GMP manufacturing environment
+ Strong understanding of supplier quality management, quality agreements, and material compliance
+ Experience managing or supporting Supplier Change Notifications (SCN) or similar processes
+ Familiarity with Quality Management Systems (QMS), preferably Veeva
+ Strong knowledge of GMP regulations and global compliance frameworks
+ Ability to work directly with external vendors and internal stakeholders
+ Strong communication, documentation, and investigation skills
** Preferred Qualifications*
* +
Experience with supplier quality in biotech or pharmaceutical manufacturing
+ Familiarity with single-use systems and material compliance investigations
+
Experience with SAP and/or Veeva systems
+ Strong understanding of supplier audits and external partner oversight programs
+ Exposure to global regulatory environments and compliance frameworks
** Core Competencies*
* + Strong supplier and stakeholder management skills
+ High attention to detail and compliance mindset
+ Ability to investigate and resolve quality issues independently
+ Strong communication and cross-functional collaboration skills
+ Ability to manage multiple supplier-related priorities simultaneously
+ Strong documentation and regulatory awareness
+ Proactive risk identification and escalation ability
** Work Environment*
* + Fully onsite role…
Position Requirements
10+ Years
work experience
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