Manager/Associate Director, US Regulatory Affairs - Kalamazoo

We are one of the fastest-growing companies in the U.S. and this may be your opportunity to join us. · Candidates need to have expert experience in RAQA (Regulatory Affairs Quality Assurance) processes as well as inbound and outbound transactions. · ...

The Associate provides review and approval of marketing and sales materials for compliance; review, revision and general maintenance of regulatory files such as adverse event reporting and state registrations. · ...

+Job summary · Manager provides regulatory guidance and strategic direction for Biological and Pharmaceutical Advertising and Promotional initiatives.+BS/MS with 3 to 5 years of experience in Animal Health Biologicals and/or pharmaceuticals Advertising and Promotion regulatory re ...

The Associate provides review and approval of marketing and sales materials for compliance; review, revision and general maintenance of regulatory files such as adverse event reporting and state registrations. · ...

The Manager provides regulatory guidance and strategic direction for Biological and Pharmaceutical Advertising and Promotional initiatives. · ...

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 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 seeking a Principal Regulatory Affairs Specialist to join our Medical Division. This Hybrid role will be based in Portage, MI, · offering the opportunity to combine on-site collaboration and remote flexibility. · This position will develop and implement environmental compl ...

++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). · ...

The successful candidate will be the regulatory strategy lead for US FDA regulated products, providing guidance and technical support for new product registrations and supplemental claims as a part of global veterinary pharmaceutical and biopharmaceutical development project team ...

We are seeking a Regulatory Affairs Associate to support regulatory submissions, · compliance activities and product lifecycle management within a highly regulated environment. · ...

+Job summary · The hire is looking to be completed in Q1 next year reporting directly into Head RA. · +Develop lead implement regulatory strategies support clinical development programs areas oncology autoimmune diseases · Plan execute regulatory submission activities Pre-IND IND ...

Our client is currently on the lookout for a Regulatory Affairs expert to develop and lead global regulatory strategies for small-molecule and biologic programs supporting clinical development across oncology and autoimmune indications. · Develop and lead global regulatory strate ...

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. ...

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 ...

Liaise with Manufacturing Regulatory Affairs and Packaging SMEs of a Lifesciences client Test Labels against Specifications and against existing Labels in Legacy Systems Bachelor s Degree in engineering or Industrial or related field with 4-6 years of experience on Manufacturing/ ...

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. · ...

+The Lead Document Controller will primarily be responsible for controlling, reviewing, releasing, archiving/storage and obsolescence of documentation. · +Responsible for all activities related to document routing. · Promptly archive and store applicable Stryker documentation. · ...