About this role
Supplier Quality Specialist Position Overview We are seeking a detail-oriented Supplier Quality Specialist to support supplier qualification, compliance, and quality management activities within a regulated manufacturing environment. This individual will partner with internal and external stakeholders to ensure suppliers meet quality, regulatory, and operational requirements while driving continuous improvement initiatives throughout the supplier lifecycle. Key Responsibilities Supplier Qualification & Management
• Support the qualification, onboarding, and ongoing management of suppliers, vendors, and service providers. • Maintain supplier qualification records, quality agreements, and associated compliance documentation. • Coordinate supplier approval activities and periodic performance evaluations. • Assist with supplier risk assessments and supplier lifecycle management activities. Supplier Quality & Compliance
• Review supplier quality documentation, audit reports, and corrective action responses. • Participate in supplier audits, assessments, and quality reviews. • Monitor supplier performance metrics and support continuous supplier improvement initiatives. • Ensure supplier activities align with applicable quality standards, regulatory requirements, and internal procedures. Change Control & Risk Management
• Manage supplier communications related to quality events, changes, and notifications. • Coordinate cross-functional impact assessments for supplier-related changes. • Support implementation and documentation of supplier change control activities. • Assist with risk assessments and mitigation strategies associated with supplier quality and supply continuity. CAPA & Issue Resolution
• Track supplier quality events, investigations, and corrective and preventive actions (CAPAs). • Partner with suppliers and internal teams to address nonconformances and quality concerns. • Monitor action item completion and ensure timely closure of quality-related commitments. • Support root cause investigations and effectiveness assessments. Cross-Functional Collaboration
• Collaborate with Quality, Manufacturing, Supply Chain, Procurement, Operations, and Technical teams. • Provide support for inspections, audits, and regulatory readiness activities. • Contribute to continuous improvement projects focused on supplier quality systems and operational excellence. Required Qualifications Education
• Bachelor's degree in Chemistry, Biology, Food Science, Engineering, Life Sciences, or a related technical discipline. • Equivalent combination of education and relevant industry experience will be considered. Experience
• 2-5 years of experience in quality assurance, supplier quality, manufacturing, or a regulated industry environment. • Experience supporting supplier qualification, supplier audits, performance monitoring, CAPA management, and change control processes. • Prior experience working within GMP, GxP, FDA-regulated, pharmaceutical, biotechnology, medical device, food manufacturing, or advanced manufacturing environments preferred. • Experience participating in internal, external, or supplier audits. Technical Knowledge Working knowledge of:
• Supplier Quality Management Systems • GMP/GxP regulations and quality standards • CAPA and deviation management • Risk assessment methodologies • Change control processes • Audit readiness and compliance programs • Quality documentation and data management systems Preferred Skills
• Supplier Quality Management • Vendor Qualification • Supplier Audits • GMP / GxP Compliance • CAPA Management • Change Control • Risk Assessment • Root Cause Investigation • Quality Systems • Continuous Improvement • Quality Assurance • Regulatory Compliance Desired Competencies
• Strong organizational and project management skills • Excellent written and verbal communication abilities • Ability to manage multiple priorities in a fast-paced environment • Strong problem-solving and analytical capabilities • Proven ability to work effectively across cross-functional teams • Detail-oriented with a commitment to quality and compliance Experience Level: Mid-Level (2-5 Years) Job Type & LocationThis is a Contract to Hire position based out of Framingham, MA. Pay and BenefitsThe pay range for this position is $38.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace TypeThis is a fully onsite position in Framingham,MA. Application DeadlineThis position is anticipated to close on Aug 31, 2026.About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.