Senior Data Privacy Regulatory Specialist - Chesterfield

We are seeking a detail-oriented Regulatory Specialist to support state regulatory activities for crop protection products. · Manage state regulatory activities for product registrations (FIFRA Sections 3, 24(c), 2(ee), 18, 5) · Communicate with state regulatory agencies regardin ...

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. · ...

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 ...

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. · ...

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 ...

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 ...

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 ...

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 ...

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 · ...

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 Specialist supports the development and implementation of regulatory and compliance programs for a chemical distribution company specializing in industrial, food, cosmetic and pharmaceutical industries. · ...

Join SSM Health as a Regulatory Specialist and play a pivotal role in ensuring compliance with healthcare regulations and standards. · ...

SMM Health as a Regulatory Specialist play a pivotal role in ensuring compliance with healthcare regulations and standards. · ...

Join SSM Health as a Regulatory Specialist and play a pivotal role in ensuring compliance with healthcare regulations and standards. · ...

This position is responsible for communicating and tracking customer specific and state agency related Regulatory Compliance information for products manufactured at all facilities including contract facilities. · Bachelor's degree with 2 years of Quality or Regulatory experience ...

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 ...