Regulatory Jobs in Plover, WI

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

RRD Plover WI is a medical device contract manufacturing facility.  The Quality/Regulatory Manager is responsible for directing planning organizing and controlling the processes procedures policies and activities for the assurance of the quality of the products according to spec More...

RRD Plover WI is a medical device contract manufacturing facility.  The Quality/Regulatory Manager is responsible for directing planning organizing and controlling the processes procedures policies and activities for the assurance of the quality of the products according to spec More...

RRD Plover WI is a medical device contract manufacturing facility.  The Quality/Regulatory Manager is responsible for directing planning organizing and controlling the processes procedures policies and activities for the assurance of the quality of the products according to spec More...

RRD Plover WI is a medical device contract manufacturing facility.  The Quality/Regulatory Manager is responsible for directing planning organizing and controlling the processes procedures policies and activities for the assurance of the quality of the products according to spec More...

RRD Plover WI is a medical device contract manufacturing facility.  The Quality/Regulatory Manager is responsible for directing planning organizing and controlling the processes procedures policies and activities for the assurance of the quality of the products according to spec More...

RRD Plover WI is a medical device contract manufacturing facility.  The Quality/Regulatory Manager is responsible for directing planning organizing and controlling the processes procedures policies and activities for the assurance of the quality of the products according to spec More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

Our client a global pharmaceutical company is seeking a clinical systems validation manager to set strategy and policies and oversight of the Validation Department and programs of related activities.This will be a 1 year contractual position with the likelihood of renewal.Job Descript More...

Team OverviewExperian is looking for a teamoriented attorney for a dynamic inhouse corporate counsel position. In this remote role you will provide legal support for Experians Marketing Services division and report into the Head of Legal.As Corporate Counsel you will provide legal sup More...