Supplier Quality Specialist Job at CNH Industrial (Shanghai)

Supplier Quality Specialist

Join our globally growing team at ATS Industrial Automation where we create comp...

Location

Canada , Cambridge

Salary:

Not provided

ATS Automation Tooling Systems Inc.

Expiration Date

Until further notice

Requirements

A post-secondary technology diploma or equivalent, specializing in toolmaking, machining, welding or mechanical engineering, mechanical technologist, quality engineering or equivalent work experience is required
ASQ CQE or ASQ SSBB or equivalent work experience is required
Nuclear Auditor training and qualification
At least 5 years in nuclear environment or other highly regulatory industry
At least 5 years of quality assurance engineering experience in a manufacturing and/or fabrication environment
Experience with the Nuclear requirements relating to Quality and Inspection plans
Demonstrated ability to work independently and to manage multiple projects from various diverse organizations
Strong working knowledge and experience working with ISO 9001, N299, NQA-1,10CFR50, 10CFR21, N285, N286, B51 and ASME Section III guidelines
Commercial Grade Dedication background and experience
Capable of being certified to Jaeger-1 Test Chart and Bausch and Lomb Vision test (including color and far- and near-distance test)

Job Responsibility

Lead the charge in sourcing and developing top tier suppliers, by providing expert guidance on technology, performance, quality, cost, logistics and delivery
Partner closely with engineering teams and suppliers to drive innovation while elevating process and quality standards
Monitor industry advancements and recommend technologies that enhance cost effectiveness, product quality, and supply chain reliability
Be a catalyst for change by actively contributing to ongoing continuous improvement initiatives
Work directly with suppliers to boost their quality output and shipping performance
Champion ABM initiatives
Conduct supplier audits to ensure full compliance with relevant industry standards and certifications (ISO 9001, CSA N299, CSA N285, NQA-1)
Strictly follow CSA N285/NQA Quality requirements as defined within the manual and procedures
Existing Supplier Development to improve KPI’s (e.g. OTD, Conformance to Specifications, Receiving issues)
Perform rough cut capacity planning and resolve gaps at ATS Approved Suppliers

What we offer

Competitive starting salaries
comprehensive health and dental benefits
overtime pay
employee bonus
RSP matching
Employee Share Purchase Program
treat days
gourmet coffee and beverages
subsidized breakfast and lunches in our cafeteria
employee referral bonuses

Fulltime

Supplier Quality Specialist

ATS is an industry-leading automation solutions provider to many of the world’s ...

Location

United States , Lewis Center

Salary:

Not provided

ATS Automation Tooling Systems Inc.

Expiration Date

Until further notice

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

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

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

Fulltime

Sr. Quality Specialist, Supplier Quality

Carex is partnering with a Pharmaceuticals industry partner to identify a Suppli...

Location

United States , Madison

Salary:

Not provided

Carex Consulting Group

Expiration Date

Until further notice

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

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

Supplier Quality Excellence Specialist

Location

India , Chennai

Salary:

Not provided

Nordex Group

Expiration Date

Until further notice

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

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

Specialist I, Supplier Quality

This position supports Supplier Quality Assurance with activities related to sup...

Location

United States , Pasadena; San Diego

Salary:

68000.00 - 80000.00 USD / Year

Arrowhead Pharmaceuticals, Inc

Expiration Date

Until further notice

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

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

competitive salaries and an excellent benefit package

Fulltime

Specialist II, Supplier Quality

The purpose of this position is to provide quality assurance support for the Sup...

Location

United States , Verona

Salary:

70000.00 - 85000.00 USD / Year

Arrowhead Pharmaceuticals, Inc

Expiration Date

Until further notice

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

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

competitive salaries and an excellent benefit package

Fulltime

Global Supplier Quality Senior Specialist

The Senior Specialist, Global Supplier Quality is responsible for driving suppli...

Location

Italy , Pomezia; Milano; Bologna; Alanno

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Minimum 7 years’ experience in supplier quality management within pharmaceuticals, medical devices, or food supplements
Strong working knowledge of GMP, ISO 13485, HACCP, and global regulatory expectations
Demonstrated success in supplier audits, risk-based quality management, and compliance oversight
Lead Auditor certification highly desirable
Bachelor’s or Master’s degree in Pharmacy, Chemistry, Engineering, or a related technical field
Proven experience using digital tools and systems for supplier qualification and performance management
Exceptional communication, stakeholder management, and problem-solving skills
Ability to operate effectively in a fast-paced, matrixed, and multicultural environment
Fluency in English required
Strong proficiency with Microsoft Office Suite and other business platforms

Job Responsibility

Lead global supplier qualification, approval, and requalification processes in alignment with corporate and regulatory standards
Develop and maintain comprehensive supplier risk assessments and qualification documentation
Oversee the full supplier lifecycle — from onboarding and performance monitoring to periodic reviews and requalification
Plan, conduct, and report supplier audits (both on-site and remote) to verify compliance with internal and external standards
Ensure adherence to GMP, ISO 13485, HACCP, and other applicable global quality and regulatory frameworks
Partner with suppliers to address audit findings, implement corrective and preventive actions, and monitor their effectiveness
Support site quality operations in reviewing and approving supplier-provided documentation, including change controls, technical files, and periodic reviews
Maintain and update Supplier Quality Agreements, ensuring alignment with internal policies and regulatory requirements
Contribute to the preparation and successful execution of regulatory inspections and customer audits related to supplier management
Proactively identify and mitigate supplier-related risks impacting product quality or supply continuity

Quality Specialist

Robert Half is seeking a Quality Specialist to support manufacturing by leading ...

Location

United States , Santa Ana

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

4–7+ years of experience in: Quality inspection
Quality technician
Manufacturing quality roles
Experience with: Nonconformance handling and MRB processes
Dispositioning parts (rework, scrap, use-as-is)
Strong ability to read and interpret: Engineering drawings
GD&T
Hands-on experience with: Calipers, micrometers (CMM exposure preferred)
Experience inspecting: Mechanical components and/or electronic assemblies (PCBA preferred)
Ability to work independently and make real-time quality decisions

Job Responsibility

Perform hands-on inspection of mechanical and electronic components (PCBA, assemblies, machined parts)
Sit at triage stations to evaluate nonconforming parts in real time
Determine appropriate disposition: Rework / fix
Escalate to MRB
Return to supplier
Support and progressively take ownership of the MRB process
Act as a secondary decision-maker on nonconformance disposition
Partner with Manufacturing and Quality Engineers to troubleshoot issues
Participate in root cause analysis and corrective actions
Support RMA and supplier-related quality activities as needed

What we offer

Medical
Vision
Dental
Life and disability insurance
401(k) plan

Fulltime

Select Country

Supplier Quality Specialist

Job Description

Job Responsibility

Requirements

Nice to have

Looking for more opportunities?

Supplier Quality Specialist

Supplier Quality Specialist

Supplier Quality Specialist

Sr. Quality Specialist, Supplier Quality

Supplier Quality Excellence Specialist

Specialist I, Supplier Quality

Specialist II, Supplier Quality

Global Supplier Quality Senior Specialist

Quality Specialist

Our AI answers in your language