Manage process improvement project portfolios in Operations with direct reporting responsibility to Quality and Process Improvement management team; employ Lean Six Sigma project management standards, including creation of charters, scope, goals, and benefits of process improvement initiatives.
The Manager of Quality, Safety and Operations Improvement will be responsible for identifying and managing quality, safety and operational improvement opportunities for key operational and clinical initiatives. Under the direction of the Chief Nursing Officer, this position will plan and manage projects related to: improving processes through decreasing variation, cost and cycle times; enhancing safety and identifying and promoting evidenced based operation and clinical performance.
In this role, you will manage, coordinate and direct the implementation and operation of metros engineering department quality assurance/quality control (qa/qc) program for all metrolink and other capital projects.
Responsible for supervising members of PLANT QA Engineering group to ensure that our Quality Control plan is effective and that our work instructions are accurate and in compliance with TS 16949 guidelines.
In this role, the selected candidate will be responsible for supervising members of PLT QA Engineering group to ensure that our Quality Control plan is effective and that our work instructions are accurate and in compliance with TS 16949 guidelines.
Evaluate, analyze and report on product and process quality performance to established quality goals.Monitor product quality through inspection testing and auditing. Establish statistically sound programs for sampling and process validations.
The Quality Assurance Drug Product Manager / TL will be primarily based in Sterile Product Manufacturing building (SPM) and the Sterile Product Support (SPS) building and will provide general oversight to MQA personnel and Floor QA personnel.
In this role, the selected candidate will provide quality oversight of Companion Diagnostic (CDx) and Diagnostics development programs at third party diagnostic sites and liaise with Clinical QA/Dev Ops as required in order to ensure the CDx programs meet device regulations and are suitable for use in Pfizer sponsored clinical trials.
In this role, the selected candidate will review and make all necessary changes to overall quality policies and procedures; work closely with Production Personnel on training, implementation, and constant analysis.
The candidate will also play a supporting role in Crowes tax publications. A successful candidate will be prepared to assist the current leadership in expanding revenue by working with practice offices on existing clients and external opportunities