Supplier Quality Specialist Job at Piper Companies (Malvern)

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

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

Quality Systems Specialist

The Baxter Healthcare Ltd Compounding Facility in Dublin operates to a Manufactu...

Location

Ireland , Dublin

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree or equivalent experience in Science or related field
post qualification experience of at least 1 years in a GMP environment, ideally in a quality role
experience in dealing with Regulatory Compliance desired
good problem solving and investigation skills would be beneficial
an ability to work in a dynamic, fast-paced and goal driven environment
be dedicated
meticulous in attention to professional standards
good professional standards and demonstrates good attention to detail
ability to work under pressure and meet deadlines
highly motivated self-starter and team worker

Job Responsibility

Ensure the compilation of Quality Management Review process
review and approval of process change controls, SOPs, NCRs and CAPAs
implementation, execution and administration of Change Control System and NCR System
administration of Recall process with the Quality management team
administration/co-ordination of risk assessments
support facility projects including process development and quality improvement initiatives
manage and maintain the Documentation System
manage site archive, storage, retrieval and destruction processes
review and approval of Quality documentation
assist in the collation of information and preparation of reports for Annual Product reviews

What we offer

Pension
Health Insurance
Life Assurance
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Food Quality Compliance Specialist

The Quality Specialist will support both business teams and suppliers in the IKE...

Location

United States , King of Prussia

Salary:

Not provided

IKEA

Expiration Date

Until further notice

Requirements

Background in food quality assurance, engineering, risk management, and production development
preferably having a food quality assurance or engineering education (2-5 years of working experience within the food industry)
Auditing experience and skills
Certification and practical knowledge of HACCP and HARPC analyses, able to identify gaps
Knowledge of Quality Management Systems and Quality tools
Are result oriented, high energy, and self-driven
Able to assess manufacturing process
Fluent in English (both written and verbal)
Comfortable with traveling up to 50-60% (air travel, domestically and internationally)
Able to drive and hold a valid driver’s license

Job Responsibility

Plan and perform food related audits and verifications and execute assessments according to IKEA standards working instructions
Support the business teams and suppliers in implementing the containment and corrective actions
Coach, inspire, and enable business teams and suppliers in the IKEA quality standards as well as in utilization of problem-solving tools in the daily work and specifically related to quality deviations to continuously maintain and improve compliance performance and create a compliance culture
Review of importers FDA Foreign Supplier Verification Program (FSVP), hazard analyses, documentation, and procedures in accordance with requirements and legislation
Lead and facilitate effective trainings for both internal and external business partners to develop competence of local, global, and IKEA-specific requirements
Update and maintain all necessary systems where reports and results are registered
Secure supplier & product quality/safety compliance following GFSI standard
Lead and participate in global/local projects related to quality
Collaborate across globe within quality matrix to develop IKEA food safety and quality policies

Fulltime

Specialist Quality Engineer

The Senior Quality Engineer leads the execution of Quality activities for medium...

Location

United States , Northampton

Salary:

Not provided

L3Harris

Expiration Date

Until further notice

Requirements

Bachelor’s Degree and minimum 4 years of prior relevant experience, or Graduate Degree and a minimum of 2 years of prior related experience. In lieu of a degree, a minimum of 8 years of directly related prior experience may be considered
Ability to obtain Secret level security clearance which requires US Citizenship
Subject matter expert in advanced problem solving (such as 8D, A3, DMAIC, RCCA)
Experience Leading and supporting FMEAs for process improvement and design
Strong proficiency in design reviews, drawing reviews, engineering change order incorporation

Job Responsibility

Evaluate and disposition customer returns, in-process defects, and address day to day quality concerns. Rapidly implementing containment and corrective actions as applicable
Support Quality leadership to ensure methodology is applied in a way that supports business performance and true alignment of business goals and objectives
Effectively communicate across multiple organizations to align a strategic and tactical path to success for manufacturing operations at the site while improving quality
Support, mentor, and guide cross-functional groups in problem solving efforts confirming root cause identification, generating corrective actions and verification items are implemented and sustained
Participate in the planning and implementation of the L3Harris Zero Defect Plan program
Generate and analyze data and metrics to prioritize corrective action and improvement activities
Participate in and support manufacturing (Gemba) and program status and scrum meetings
Plan, analyze, survey and control to assure that all applicable quality requirements are adhered to in all phases of a program, from initial proposal through end customer acceptance
Review new contracts to determine the quality assurance requirements and flow down requirements to the appropriate level
Participate in Engineering design reviews, review engineering drawings for conformance to quality requirements and sign off on approved drawings

Quality Assurance Specialist - Warehouse/Supply chain

Join a global leader in Burgess Hill, supporting their warehouse and inspection ...

Location

United Kingdom , Burgess Hill

Salary:

18.94 - 21.73 GBP / Hour

Office Angels

Expiration Date

Until further notice

Requirements

Experience in quality assurance or inspection within aerospace or automotive or manufacturing environments
Strong understanding of supply chain processes / root cause analysis
Confidence using systems such as SAP or similar ERP tools
A proactive mindset focused on continuous improvement and problem-solving

Job Responsibility

Investigate recurring quality issues with incoming parts
Engage directly with suppliers to understand root causes of non-conformance
Analyse inspection results and determine whether issues stem from the parts, the process, or the system
Review and improve inspection procedures to ensure accuracy and consistency
Collaborate with internal teams to ensure quality standards are upheld across the supply chain
Use systems like SAP to track quality data, supplier performance, and inspection outcomes

Fulltime

Quality Assurance Specialist II

The Quality Assurance group develops and maintains a world-class Quality Managem...

Location

Canada , Saint-Laurent

Salary:

Not provided

Randstad

Expiration Date

January 25, 2026

Requirements

D.E.C. (Diploma of College Studies) in Mechanical or Electrical Engineering (or technical training with equivalent experience)
5+ years of experience in a manufacturing environment
Experience in internal and external (supplier) auditing required
Knowledge of ISO 9001:2015 and its quality management principles
Knowledge of manufacturing processes related to mechanical or electrical products (welding, plating, painting, machining, sheet metal, mechanical/electrical assembly, PCB assembly, cable assembly)
Bilingual (French and English)
Excellent ability to communicate both orally and in writing

Job Responsibility

Execute the complete audit process cycle—plan an audit, conduct an audit, report/communicate the results, and issue corrective actions if necessary
Ensure product compliance with design requirements based on a quality plan—develop inspection and test standards, establish control points, supervise the inspection process, and process non-conformities through resolution plans
Ensure the maintenance of manufacturing requirements—review, assign responsibility, and determine the material disposition of a non-conformity
conduct investigations to determine root causes and necessary corrective actions for material issues
update/develop the standards used to accept/reject parts
set up quality clinics
Lead MRB (Material Review Board) meetings and provide necessary recommendations
Execute quality audits in the Production area
Validation and verification of manufacturing processes as well as qualification techniques
Deployment of production measures to generate continuous improvement projects

Fulltime

Quality and Lean Specialist

We are on the lookout for a QA & Lean Specialist for our Rydalmare site. In this...

Location

Australia , Rydalmere

Salary:

Not provided

Hunter Douglas

Expiration Date

Until further notice

Requirements

Hands-on, technically minded professional with strong problem-solving skills and a passion for continuous improvement
Experience in quality and Lean practices in a production or warehouse environment
Ability to communicate clearly, lead by example, and influence at all levels
Thrive on driving efficiency, coaching teams, and delivering high standards every day

Job Responsibility

Lead and maintain quality control programs across fabrication and warehouse operations, ensuring adherence to internal standards and customer expectations
Analyse quality data, customer feedback, and production reports to identify trends, root causes, and improvement opportunities
Implement and champion Lean Manufacturing tools and techniques to streamline processes, reduce waste, and drive continuous improvement
Coach and upskill teams in problem solving, visual management, root cause analysis, and performance gap resolution
Collaborate with cross-functional teams to resolve supplier quality issues and ensure accurate procurement specifications
Oversee the non-conformance and dispensation processes, including documentation, investigation, and corrective actions
Coordinate calibration schedules for equipment and maintain quality assurance records and compliance documentation
Monitor delivery performance metrics and lead initiatives to improve order fulfilment accuracy and timeliness

What we offer

Access to Club Social – exclusive benefits and events
On-site parking for convenience and ease
Signature career development opportunities to help you grow professionally
Generous employee discount on our products
Be part of an amazing culture with strong collaboration across teams

Supplier Quality Specialist

Piper Companies

Location:
United States , Malvern

Category:
Quality Control

Contract Type:
Contract work

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 04, 2026

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