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Site Quality Assurance Manager – Phoenix

Stryker Group

This is a Full-time position in Phoenix, AZ posted May 2, 2021.

Site Quality Assurance Manager – Phoenix

Stryker is one of the world’s leading medical technology companies and, together with our customers, is driven to make healthcare better.

We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.

We are proud to be named one of the World’s Best Workplaces and a Best Workplace for Diversity by Fortune Magazine.

Learn more about our award-winning organization by visiting

Who we want
Managers who drive performance.

People who implement process improvements and leverage the talent of their team to consistently increase performance and productivity Quality-focused team drivers.

People who push their team to deliver the highest quality products and solutions in a timely manner.

Talent developers.

Growth-oriented managers who recruit and hire top-performing talent and prioritize the development of their team members.

What you will do

Stryker’s Global Quality team is looking for a Site Quality Assurance Manager in Phoenix.

As Manager you will l ead the Quality Assurance team at the Phoenix site with focus on QA activities and delivering key quality and compliance results for the site operations.

You will lead Quality Assurance team that is responsible for product and process performance and continuous improvement of quality assurance programs.

You will drive programs and initiatives aimed to achieve Quality performance targets in areas such as NCs, CAPAs, first pass yield, supplier DPM, manufacturing loss and escape reductions.

You will support all functions of the QA team personnel including (but are not limited to): incoming and manufacturing process quality, production control functions, NC/CAPA activities, quality system improvements, audit support (both internal and external), inspection optimizations, resolve issues on the production lines, investigate line downs and holds, continuously improve process capability to deliver on the Quality Vision and investigate and support any manufacturing/supplier related recalls.

You will be responsible for executing internal and external agency site audits/inspections.

May serve as Management Representative for the site and presents to Management with Executive Responsibility regularly on the status of the site’s QS You will champion a positive employee relations environment by promoting open communication, engagement and development of team members.

Promotes a culture of inclusiveness, trust, flexibility and teamwork.

You will represent Site Quality Operations at appropriate Divisional Forums including but not limited to Management Review, CAPA Review Board, NCMB You will partner with Division RAQA Leaders and DOL (Division Operations Leader) to represent GQO QA for the SSS Franchise.

You will ensure development of talent in expertise domains of partner divisions Develop and implement quality strategies with the quality planning process that align with site, region and global QA vision.

What you need
Bachelor’s Degree in engineering or related discipline Minimum of 10 years’ experience in a technical role and or leading a team of high performing individuals.

Ideally 5 years of which in a Quality Management position in the Medical, Pharmaceutical, Bio-Medical/Pharma or Automotive manufacturing environment.

Experience of managing inspections/audits by the FDA and other regulatory bodies highly preferred Knowledge of 21 CFR Part 820 and ISO 13485 highly preferred Knowledge of quality tools such as SPC / Process Control, FMEA, Problem Solving / Root Cause Analysis, Poka-Yoke, and other Six Sigma tools highly preferred
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