Regulatory Affairs Specialist - St. Louis

We are seeking a motivated and detail-oriented Regulatory Affairs Specialist with approximately one year of experience working with the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). · This role supports regulatory compliance activities for pesticide products, ensur ...

The Regulatory Affairs Specialist - Publishing is responsible for leading the electronic publishing process and providing end-to-end submission support to the North America regulatory team. · ...

We are seeking a motivated and detail-oriented Regulatory Affairs Specialist with approximately one year of experience working with the Federal Insecticide, Fungicide, · and Rodenticide Act (FIFRA).This role supports regulatory compliance activities for pesticide products, ...

We are seeking a motivated and detail-oriented Regulatory Affairs Specialist with approximately one year of experience working with the Federal Insecticide, · Fungicide, and Rodenticide Act (FIFRA).This role supports regulatory compliance activities for pesticide products, · ensu ...

+ Reporting to the Senior Manager, Regulatory Affairs within the RA Department, the incumbent is responsible for supporting the development and administration of STERIS's global regulatory responsibilities. · +Bachelor's Degree · At least 5 years professional experience including ...

We are seeking an experienced Regulatory Affairs Specialist to join our team. · The Regulatory Affairs Specialist will be responsible for preparing, submitting and managing regulatory applications and documentation for products governed by U.S. regulations-including pesticide pr ...

We are proactively building a team of highly qualified Public Affairs Historical Research Specialists to support a potential government contract. · This opportunity is contingent upon the award of the contract. If awarded, this contract will provide a unique opportunity to contri ...

Immediate Need for Regulatory Affairs Specialist in Chesterfield MO. · ...

We are seeking two detail-oriented Regulatory Affairs Specialists to join our team— based in the St. Louis area.In this high-impact role, you will be the backbone of our state regulatory operations, ensuring our crop protection products meet all legal and environmental standards ...

TekWissen is a global workforce management provider that offers strategic talent solutions to clients worldwide. The client is a German multinational pharmaceutical and biotechnology company. · ...

We are seeking two detail-oriented Regulatory Affairs Specialists to join our team— based in the St. Louis area.In this high-impact role, you will be the backbone of our state regulatory operations, ensuring our crop protection products meet all legal and environmental standards ...

The General Affairs Specialist will support expatriation and immigration services for employees as needed. · ...

We are seeking two detail-oriented Regulatory Affairs Specialists to join our team— based in the St. Louis area. · ...

The Supervisory Public Affairs Specialist serves as the Supervisory Public Affairs Officer (PAO) at VA St. Louis Health Care System (VASTLHCS). · ...

The CMC Regulatory Affairs Associate will support regulatory submission activities with a strong focus on Chemistry, Manufacturing and Controls. This role is hands-on and centered on authorizing reviewing managing Module section for CTD eCTD submissions within pharmaceutical envi ...

This client is a German multinational Pharmaceutical and biotechnology company and one of the largest pharmaceutical companies in the world... · ...

We are seeking a dedicated and detail-oriented individual to join our team for a six-month role with the potential for extension based on performance. In this position, you will play a crucial role in managing state regulatory activities related to crop protection products.Commun ...

The Regulatory Affairs Associate responsibilities encompass the support of US FDA applications (NDAs, ANDAs, DMFs) and support of Regulatory activities including but not limited to: Plan/author/compile/submit statutory reports in eCTD format for marketed products per FDA requirem ...

The Regulatory Affairs Associate responsibilities encompass the support of US FDA applications (NDAs, ANDAs, DMFs) and support of Regulatory activities including but not limited to: · Plan/author/compile/submit statutory reports in eCTD format for marketed products per FDA requir ...

The Sr. Specialist, Americas Operations for the Government Affairs & Policy (GAP) team will play a critical role in managing financial operations, supplier relationships, and contract lifecycles across the U.S., Canada, Latin America, and Caribbean regions.This position supports ...