CrawlJobs Logo

Supplier Quality Specialist

United States, Lewis Center · Job Posted January 07, 2026
Apply Position
Job Link Share

Job Description

ATS is an industry-leading automation solutions provider to many of the world’s most successful companies. ATS Industrial Automation is expanding the capabilities of its existing nuclear division into the US. With over 20 years of experience in bringing automation to nuclear projects, ATS provides world-leading automation tooling to the nuclear energy sector for new reactor builds, refurbishment, operations, and maintenance.

Job Responsibility

  • Provide technical expertise and leadership to sourcing and development of suppliers with respect to technology, performance, quality, cost, logistics and delivery
  • Collaborate with suppliers and engineering teams on process and quality improvements
  • Stay up to date with technological advancements in the field and identify how to leverage them to improve cost, quality or assurance of supply
  • Contribute to continuous improvement activities
  • Direct engagement with suppliers to accomplish improvements in supplier quality and shipping performance
  • Audit the supplier to applicable codes and standards (ISO 9001, NQA-1)
  • Strictly follow ISO/NQA-1 Quality requirements as defined within the manual and procedures
  • Benchmarking new potential suppliers (pre-audit)
  • Supplier scorecard delivery and follow up
  • On-going Supplier engagement ensuring both ATS and Suppliers are informed and in compliance with change management
  • Support Product Sourcing Strategy and provide technical leadership in new supplier selection
  • Support new business ramp with Suppliers (drawing reviews, Inspection plans, etc.)
  • Assist the Quality Department with SCAR resolution, more complex NCR’s, external Supplier training, and Audits as assigned by the Quality Manager
  • Travel may be required to local and international destinations

Requirements

  • A post-secondary engineering, quality or equivalent degree, with experience in mechanical engineering, manufacturing, toolmaking, machining, welding, quality or equivalent experience is preferred
  • Ability to meet the qualifications of NIAC Lead Auditor
  • Minimum 5 years experience in nuclear environment or other highly regulated industry preferred
  • Minimum 5 years experience in a calibration environment preferred
  • Minimum 5 years experience working in an environment with applications in: manufacturing, mechanical equipment & components, heat treating, plating, welding & painting applications preferred
  • Working experience with ISO 9001 and NQA-1
  • Experience with the Nuclear requirements relating to Quality and Inspection plans
  • Advanced understanding of GD&T
  • Ability to read mechanical detail and assembly drawings
  • Ability to read a variety of types of measuring equipment
  • Ability to operate and program a CMM
  • Strong communication and documentation skills
  • Demonstrated ability to work independently and to manage multiple projects from various diverse organizations

Nice to have

Nuclear Auditor training and qualification is an asset

What we offer

  • Flexible work schedules
  • Employee events
  • Free coffee beverages
  • Employee referral program
  • Safety shoe programs
  • Overtime pay eligibility
  • Paid vacation
  • Company paid short- and long-term disability and life insurance
  • Comprehensive health benefits
  • 401K matching program
  • Employee Incentive Bonus program
  • Optional Employee Share Purchase Program
  • Tuition reimbursement programs

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Supplier Quality Specialist

8 matching positions

Supplier Quality Specialist

The Supplier Quality Specialist ensures the quality and reliability of materials...
Location
Location
China , Shanghai
Salary
Salary:
Not provided
cnhindustrial.com Logo
CNH Industrial
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BE / B.Mechanical / Metallurgical
  • Has knowledge of Driveline system, special for gear &shaft, Gearbox & Transmission working structure and theory
  • Min. of 8 years of working experience in industrial field
  • Worked in Gearbox/Transmission manufacture company is preferred, at least 5 years of experience in quality engineering/project management position
  • Worked in Automotive OEM or Agriculture/Construction machine company is also priority considered, at least 3 years of experience with supplier quality engineering responsible for gearbox/transmission
Job Responsibility
Job Responsibility
  • Support the global product development process for new products and ensure that suppliers meet CNH requirements
  • Assess and monitor supplier performance to ensure compliance with quality standards and specifications
  • Conduct supplier audits and inspections to identify areas for improvement and ensure adherence to requirements
  • Investigate and resolve supplier-related quality issues, including root cause analysis and corrective actions
  • Collaborate with suppliers and internal teams to implement quality improvement initiatives
  • Maintain and update supplier quality documentation and reports
  • Support the qualification and onboarding of new suppliers through evaluations and approvals
  • Fulltime
Read More
Arrow Right

Sr. Quality Specialist, Supplier Quality

Carex is partnering with a Pharmaceuticals industry partner to identify a Suppli...
Location
Location
United States , Madison
Salary
Salary:
Not provided
carexconsulting.com Logo
Carex Consulting Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in a scientific field
  • Minimum of 8 years of experience in pharmaceutical or biotechnology quality, including at least 4 years in supplier quality
  • Strong knowledge of FDA, EMA, ICH, GxP, and GDP regulations
  • Experience managing supplier quality systems, including SCARs and change notifications
  • Excellent communication skills with the ability to collaborate across diverse teams and external partners
  • Strong attention to detail, organizational skills, and a proactive problem-solving mindset
  • Experience with electronic document management systems in regulated environments preferred
  • Proficiency with Adobe Acrobat, Microsoft Office, DocuSign, and SmartSheet preferred
  • Ability to work independently, manage priorities, and operate effectively in a fast-paced environment
  • Strong interpersonal, verbal, and written communication skills with a professional approach to external interactions
Job Responsibility
Job Responsibility
  • Manage Supplier Corrective Action Requests (SCARs) and Supplier Change Notifications (SCNs), ensuring timely assessment, resolution, and effectiveness
  • Guide and coach stakeholders on SCAR and SCN processes to promote consistency and strengthen quality culture
  • Support cross-functional evaluation of supplier changes and corrective actions, including impact assessments and follow-up activities
  • Oversee quality agreement lifecycle management, including drafting, reviewing, approving, and maintaining compliance with periodic reviews
  • Assist in establishing and tracking Supplier KPIs and contribute to Quality Management Reviews and Business Review meetings
  • Maintain current knowledge of regulatory requirements and compliance expectations related to drug development
  • Author, review, and maintain procedural documentation such as SOPs, work instructions, policies, and forms
  • Support regulatory inspections as a subject matter expert
  • Ensure compliance with cGMP, 21 CFR, USP, EP, and ICH standards
  • Perform additional responsibilities aligned with the role as needed
  • Fulltime
Read More
Arrow Right
New

Supplier Quality Specialist (Electronics)

Hunter Douglas is the world's leading manufacturer of window coverings and a maj...
Location
Location
Mexico , Rosarito
Salary
Salary:
Not provided
hunterdouglas.com Logo
Hunter Douglas
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Electronics Engineering or related field
  • 7+ years of experience in Supplier Quality, Manufacturing Quality, or Electronics Engineering
  • Strong experience with electronic components (PCBA, IPC Standards, semiconductors, etc.)
  • Proven track record in resolving complex, chronic electronic supplier quality issues
  • Hands-on experience managing and approving PPAPs
  • Deep knowledge of quality tools: PFMEA, Control Plans, MSA, SPC, 8D
  • Familiarity with IPC standards (e.g., IPC-A-610, IPC-J-STD-001)
  • Understanding of electronics manufacturing processes (SMT, wave soldering, testing)
  • Excellent communication and stakeholder management skills
  • Ability to influence suppliers and internal teams without direct authority
Job Responsibility
Job Responsibility
  • Act as the technical authority on electronic components, including PCBs, PCBAs, transmissions, and motors
  • Provide guidance on industry standards (IPC and applicable regulatory standards)
  • Support design reviews (DFMEA, PFMEA) to ensure quality is built into the product and process
  • Advise internal teams and suppliers on best practices in electronics manufacturing and quality assurance
  • Utilize structured problem-solving methodologies, 8D/DMAIC, A3, etc., to lead root cause analysis and corrective actions for chronic and high-impact supplier quality issues
  • Drive permanent corrective actions and validate their effectiveness
  • Analyze supplier performance data to identify trends and proactively mitigate risks
  • Escalate critical issues and lead cross-functional containment and recovery plans
  • Lead and coordinate the PPAP process for electronic components and assemblies, ensuring all PPAP elements (PSW, control plans, MSA, capability studies, etc.) meet requirements
  • Review and approve supplier documentation for completeness and compliance
What we offer
What we offer
  • Annual base salary
  • Annual bonus
  • Generous benefits package including medical, dental, vision, life
  • A company culture that prioritizes internal development and professional growth
  • Time off with pay (3 days annual)
  • Christmas bonus
  • Savings fund
  • Fulltime
Read More
Arrow Right

Supplier Quality Excellence Specialist

Location
Location
India , Chennai
Salary
Salary:
Not provided
nordex-online.com Logo
Nordex Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in business or engineering
  • 5+ years in supplier Quality or Quality engineering experience in implementing quality improvement programs
  • Knowledge of structured data analysis, statistics and data techniques for supplier performance analysis and reporting
  • Ability to supervise projects and direct cross-functional teams
  • Good level of understanding on Supplier Quality development process, supply chain Performance Management
  • Experience in advanced reporting, dashboards and other solutions using tools like Power BI, Advance Excel, SQL, Excel, SharePoint
  • Team-oriented professional with strong independent judgment and proactive approach in change management
  • Highly motivated, action-oriented, and committed to achieving tasks and targets with a problem-solving mindset
  • Skilled communicator, capable of working effectively with stakeholders at all business levels
  • Proficient in delivering engaging and clear presentations to diverse audiences
Job Responsibility
Job Responsibility
  • Monitor, improve, and develop suppliers through performance monitoring to support Supplier Quality Development activities
  • Designing, implementing, and maintaining systems to audit, evaluate, and monitor supplier performance
  • Establishment of supplier performance analysis and reporting like Supplier score card, KPI reporting, Risk Management and data management
  • Contribute to data-based continuous quality improvement
  • Collaborate with global team, Stakeholders to identify continuous improvement opportunities to further develop and deploy SQA processes, approaches
  • Escalation of critical supplier QHSE performance issues to drive Supplier quality improvement projects (SQIPs) by SQA owners
  • Facilitate and follow up on escalated corrective actions and lessons learned transferred to SQA process improvements
  • Strengthen relationships with suppliers and internal stakeholders (Sourcing, SQA, HSE, Engineering, Manufacturing Sustainability etc.) to promote collaboration and clarity
  • Support the onboarding process for new suppliers and train them on new processes, tools, and products to ensure compliance with company standards
Read More
Arrow Right

Specialist I, Supplier Quality

This position supports Supplier Quality Assurance with activities related to sup...
Location
Location
United States , Pasadena; San Diego
Salary
Salary:
68000.00 - 80000.00 USD / Year
arrowheadpharma.com Logo
Arrowhead Pharmaceuticals, Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associate’s degree, with BS/BA preferred
  • 1+ year of quality assurance experience
  • Ability to follow company procedures, work instructions, and policies
  • Competent knowledge of and ability to use Microsoft Word, Outlook, PowerPoint and Excel
  • Excellent attention to detail and organizational skills
  • Ability to multi-task and prioritize work with minimal supervision
  • Excellent interpersonal, verbal, and written communication skills
Job Responsibility
Job Responsibility
  • Manage initial intake of new regulated suppliers from the business teams
  • Conduct or assist with supplier risk assessments
  • Coordinate with internal and external auditors performing supplier audits
  • Maintain supplier, audit, and qualification records within Veeva
  • Support Lead Auditors by tracking timelines and preparing required documentation
  • Maintain supplier licenses, certifications, and related compliance documentation within Veeva
  • Generate and distribute supplier metrics to QA groups and business stakeholders
  • Support Arrowhead audits and inspections
  • Assist with preparation, update, review, and routing of Arrowhead procedural documents
  • Support eQMS and other system implementations
What we offer
What we offer
  • competitive salaries and an excellent benefit package
  • Fulltime
Read More
Arrow Right

Specialist II, Supplier Quality

The purpose of this position is to provide quality assurance support for the Sup...
Location
Location
United States , Verona
Salary
Salary:
70000.00 - 85000.00 USD / Year
arrowheadpharma.com Logo
Arrowhead Pharmaceuticals, Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry is preferred
  • 3 years of quality assurance experience in a biotech or pharmaceutical development, manufacturing, or contract manufacturing organization with an emphasis on Supplier Quality
  • Working knowledge of 21 CFR Parts 210/211, ICH Q7, and applicable global regulatory expectations (e.g., FDA, EMA, Health Canada), along with familiarity with relevant regulatory guidance documents
Job Responsibility
Job Responsibility
  • Support supplier qualification, requalification, and ongoing monitoring activities for raw material suppliers, CMOs, contract laboratories, packaging vendors, and service providers
  • Assist with supplier risk assessments and ensure documentation is current and compliant
  • Collaborate with stakeholders and suppliers, as needed, on quality events and non-conformances and issue supplier corrective action requests, as outlined in the applicable quality agreements
  • Assist with maintenance of approved supplier lists and supplier quality records
  • Review and assess supplier change notifications for quality and regulatory impact
  • Ensure timely and accurate documentation within the Quality Management System (QMS)
  • Track and trend supplier performance metrics (e.g., deviations, on-time CAPA closure, audit findings)
  • Identify recurring issues and support continuous improvement initiatives
  • Assist with preparation, update, review, and routing of Arrowhead procedural documents
  • Assist with other QA duties as needed
What we offer
What we offer
  • competitive salaries and an excellent benefit package
  • Fulltime
Read More
Arrow Right
New

Specialist Quality Assurance

Amgen is one of the world’s leading independent biotechnology companies. For ove...
Location
Location
Singapore , Singapore
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree OR Master’s degree and 2 years of directly related experience OR Bachelor’s degree and 4 years of directly related experience OR Diploma and 8 years of directly related experience
  • 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems
  • Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff
  • Experience with regulatory audits and inspections
  • Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality
Job Responsibility
Job Responsibility
  • Provide Quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
  • Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicator met targeted metrics
  • Co-lead and support the deployment of Amgen quality systems, including management review, validation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations
  • Participate in complex root cause investigations for deviations
  • Review and approve deviation investigations, change controls, and other quality records (with focus on highly complex records)
  • Provides Quality Assurance support in New Product Introduction (NPI) team
  • Coach site Quality Assurance professionals on resolution of complex problems
  • Participate in regulatory inspections, and interact directly with regulatory inspectors
  • Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
  • All medical related expenses incurred from this medical check shall be borne by the company
  • Fulltime
Read More
Arrow Right

Audit Quality Specialist

Membership Bespoke is delighted to be supporting a globally recognised membershi...
Location
Location
United Kingdom , Ashford
Salary
Salary:
55000.00 GBP / Year
membershipbespoke.co.uk Logo
Membership Bespoke
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Recognised Internal Auditor qualification
  • Recognised Lead Auditor qualification
  • Experience working within quality assurance, certification, accreditation, compliance or audit environments
  • Strong knowledge of audit methodologies and quality management systems
  • Excellent communication and stakeholder management skills
  • Experience of ISO-based standards and audit frameworks
  • Experience in external, certification, accreditation or supplier auditing
  • Audit quality assurance and report review
  • Managing, mentoring or developing auditors
  • Auditor calibration and competence assessment
Job Responsibility
Job Responsibility
  • Drive consistency, quality and continual improvement across the audit programme
  • Review audit reports and provide constructive feedback to auditors
  • Monitor auditor performance and identify opportunities for development and improvement
  • Support auditor calibration and promote consistent interpretation of standards and audit findings
  • Conduct internal audits and support risk-based audit planning activities
  • Analyse audit data and trends to identify risks, opportunities and areas for improvement
  • Produce management reports and quality metrics
  • Develop and enhance audit procedures, guidance and best practice documentation
  • Support auditor recruitment, onboarding and ongoing competence development
  • Ensure compliance with relevant quality, governance and certification standards
What we offer
What we offer
  • Free parking
  • Fulltime
Read More
Arrow Right