Principal Regulatory Affairs Specialist - Portage

We are currently seeking a Senior Regulatory Affairs Specialist to join our Acute Care business unit based hybrid three days per week in Portage, Michigan. Stryker impacts more than 150 million patients annually. · ...

We are seeking a Principal Regulatory Affairs Specialist to join our Medical Division. This Hybrid role will be based in Portage, MI. · This Hybrid role will be based in Portage, MI, offering the opportunity to combine on-site collaboration and remote flexibility. · The job requi ...

We are currently seeking a Senior Regulatory Affairs Specialist to join our Acute Care business unit based hybrid three days per week in Portage Michigan. · Evaluate device modifications and takes appropriate action to ensure global product compliance. · Support new product devel ...

We are currently seeking a Senior Regulatory Affairs Specialist to join our Acute Care business unit based hybrid three days per week in Portage, Michigan. · ...

++We are seeking a Principal Regulatory Affairs Specialist to join our Medical Division. · ++Develop and implement global product environmental compliance strategies to meet international, federal, state, and local regulations (e.g., RoHS, REACH, WEEE). · ...

This position is posted by Jobgether on behalf of a partner company looking for a Regulatory Affairs Specialist - REMOTE. This global team focuses on ensuring regulatory compliance for innovative healthcare products. · Assist with the implementation of global regulatory roadmaps. ...

The Lead Document Control Specialist is responsible for the control review release archiving storage and obsolescence of quality documentation for site operations. · ...

+The Lead Document Control Specialist is responsible for the control, review, release, archiving, storage and obsolescence of quality documentation for site operations. · Manage all activities related to document routing distribution and release to ensure availability of current ...

This position is responsible for all activities related to document routing, distribution and release to assure that the latest effective copies are available as required. Ensures prompt archiving and storage of applicable Stryker documentation. Provides timely retrieval of docum ...

Lead Document Controller will control review release archiving/storage obsolescence of documentation for Client site(s). Assist sites periodic reviews CIDTs post release tasks ensure completion according applicable regulatory requirements standards. ...

The Senior Clinical Evaluation Specialist applies scientific, regulatory and project management skills to establish the evaluation strategy and compile a body of clinical evidence, · in order to reach a legally binding scientific conclusion on the safety and performance of medica ...

The Senior Clinical Evaluation Specialist applies scientific and project management skills to establish the evaluation strategy and compile a body of clinical evidence for medical devices throughout their product lifecycle. · This role is Remote supporting our Instruments Divisio ...

+ Establish the evaluation strategy and compile a body of clinical evidence to reach a legally binding scientific conclusion on the safety and performance of medical devices throughout their lifecycle. · + Support compliant literature search strategies and perform complex literat ...

This job involves responsible for all activities related to document routing, distribution and release to assure that the latest effective copies are available as required. · ...

The Lead Document Controller will be primarily responsible for the control, review, · release, archiving/storage, and obsolescence of documentation for Client site(s), including procedures · and specifications. · ...

The Senior Clinical Evaluation Specialist applies scientific, regulatory and project management skills to establish the evaluation strategy and compile a body of clinical evidence, in order to reach a legally binding scientific conclusion on the safety and performance of medical ...

+ Job summary: The Senior Clinical Evaluation Specialist applies scientific, regulatory and project management skills to establish the evaluation strategy and compile a body of clinical evidence, in order to reach a legally binding scientific conclusion on the safety and performa ...

The Lead Document Controller will be responsible for the control and review of documentation for client sites. · Responsible for all activities related to document routing, distribution and release. · Prompt archiving and storage of applicable client documentation. · ...

A Lead Document Controller for a medical devices and equipment manufacturing company is needed in the Kalamazoo area.This role is focused on managing the compliant release and lifecycle of medical device documentation within a PLM system, · ensuring all records meet strict global ...

Western Michigan University invites applications for the position of Faculty Specialist II – Clinical Specialist in the WMU Bronson School of Nursing. · ...