Lead Quality Analyst

Lead Quality Analyst

Job Description

You were made to create Better Care for a Better World: as a person, you’re a problem-solver – a connector – someone who thrives on creating order from complexity and driving continuous improvement.

You see the big picture while mastering the details, ensuring that every product, process, and partnership flows with precision and purpose.

You live your life in alignment with the highest values of integrity, efficiency, and collaboration, always working to turn today’s challenges into tomorrow’s success stories.

In this role, you’ll help us deliver better care for billions of people around the world.

It starts with YOU.

About You

In one of our Quality roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.

This role will also:



* Own site Quality Management Systems, including ETQ modules, Approved Supplier Process, Equipment Calibration, and Document Control.


* Lead CAPA and Quality Nonconformance processes, including initiation, investigation, follow‑up, and closure for assigned systems..


* Support audit readiness and QA training, including participation on Audit Readiness teams.


* Ensure compliance with GMP, ISO, FDA, Health Canada, and other applicable regulations.


* Develop, execute, and sustain continuous improvement initiatives for existing and new quality processes.


* Provide quality systems technical expertise to business teams, suppliers, and cross‑functional partners.


* Develop and maintain systems and processes for quality records, documentation, inspection, sampling, and statistical process control.


* Build and sustain organizational capability in quality systems, standards, and regulatory requirements.


* Partner with stakeholders to deliver quality solutions that meet business, customer, and compliance needs.

To succeed in this role, you will need the following qualifications:

Required Qualifications



* Bachelor’s degree in science, engineering or related discipline.


*  3+ years of broad experience in Quality, Manufacturing, Research or Regulatory function or equivalent experience


* Experience should include close working relationships with customer functions, good breadth of knowledge of applicable FDA, Health Canada, and requirements for formulated cosmetics and medical device products.


* Demonstrated application of LEAN/ Continuous Improvement skills, and demonstrated skill as a trainer.

Preferred Qualifications



* Six Sigma Certified Black or Green Belt, ASQ-Certified Quality Engineer, Certified Quality Auditor, and ISO 9001 or 13485 Lead Auditor Certification is preferred.


* Strong analytical skills including trend and statistical analysis.


* Prior leadership experience with moderate to large sized projects or systems.

Led by Purpose.

Driven by You.

Total Benefits

We believe that our employees are our great...