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. 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). · ...

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 ...

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. · ...

We are partnered with a fast-growing medical device manufacturer to identify an exceptional FDA/PMA Regulatory Affairs Expert. · This individual will serve as the company's senior regulatory authority, owning FDA strategy, PMA and 510(k) submissions, · and all high-level engageme ...

Job Title: Regulatory Affairs Specialist II · Location: Princeton, NJ · Duration: 11 Months · Work Schedule: · Onsite – 5 days per week Normal business hours · Job Summary · Experienced regulatory professional responsible for supporting the development and execution of regulatory ...

The salary range for this position is between $185k and $240k. · Actual salary at the time of hire may vary and may be above or below the range based on various factors, including, but not limited to, the candidate's relevant qualifications, skills, and experience. The company al ...

Executive Director, Regulatory Affairs, Advertising & Promotion – Permanent – New Jersey · Proclinical is seeking an Executive Director, Regulatory Affairs, Advertising & Promotion for a successful global pharmaceutical company based in New Jersey. · Primary Responsibilities: · I ...

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. ...

Zoetis is currently seeking a Companion Animal Clinical Development Clinician to join our team in Kalamazoo, MI. In this role, you will design and execute companion animal pharmaceutical and biopharmaceutical clinical development studies in compliance with U.S. CVM/CVB regulatory ...