Regulatory Affairs Specialist - Chesterfield

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

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

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 ...

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 ...

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

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 a skilled Regulatory Affairs Specialist to join our dynamic team for a 6-month role with the possibility of extension based on performance. · Support the team in managing state regulatory activities to obtain and maintain registrations, · Communicate with state reg ...

We are seeking a skilled Regulatory Affairs Specialist to join our dynamic team for a 6-month role with the possibility of extension based on performance.This position offers two opportunities: · one based in St. Louis with a hybrid work arrangement · another fully remote · ...

This position involves managing state regulatory activities to support business operations including state registration activities for Environmental Science products. The candidate will also compile and submit required data and documents necessary for registration across all Stat ...

Job summary: · We are seeking a skilled Regulatory Affairs Specialist to join our dynamic team for a 6-month role with the possibility of extension based on performance.Support the team in managing state regulatory activities to obtain and maintain registrations. · Communicate wi ...

The candidate will support the team in managing state regulatory activities necessary to obtain and maintain registrations. · ResponsibilitiesCommunicate with State regulatory agencies regarding submissions approvals renewals etc. · Maintain and update regulatory databases other ...

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 ...

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 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 ...

Job Title: Regulatory Affairs Specialist · Job Description · The Regulatory Affairs Specialist plays a crucial role in supporting US FDA applications (NDAs, ANDAs, DMFs) and international drug product applications. This position involves planning, authoring, compiling, and submit ...

+h2>Job summary · The Regulatory Affairs Specialist plays a crucial role in supporting US FDA applications (NDAs, ANDAs, DMFs) and international drug product applications. · +/h2>Plan statutory reports in eCTD format for marketed products per FDA requirements. · Review CMC regula ...

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

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 ...

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. · ...