Job Summary
Under general supervision, the Regulatory Specialist is responsible for planning and executing regulatory activities necessary to bring new Over-the-Counter (OTC) Drugs and Cosmetics to...
The Role: Be the Driving Force Behind Every BuildAs a Commercial Construction Project Manager, you will own your projects from start to finish.You’ll work alongside a dedicated team of Site Superinten...
read moreThe Role: Be the Driving Force Behind Every BuildAs a Commercial Construction Project Manager, you will own your projects from start to finish.You’ll work alongside a dedicated team of Site Superinten...
read moreDaily Guarantee plus Commission pay.Earning potential up to $90,000 per year.Competitive pay and benefits, including Day 1 Health & Wellness Benefits, Employee Stock Purchase Plan, 401K Employer Match...
read moreWe are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, or a related field. Ensure regu...
read moreWe are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, or a related field. Ensure regu...
read moreDaily Guarantee plus Commission pay.Earning potential up to $90,000 per year.Competitive pay and benefits, including Day 1 Health & Wellness Benefits, Employee Stock Purchase Plan, 401K Employer Match...
read moreMust be able to prioritize and provide input on regulatory aspects. This individual provides support to internal and external customers in order to ensure that all domestic and global regulatory requi...
read moreMust be able to prioritize and provide input on regulatory aspects. This individual provides support to internal and external customers in order to ensure that all domestic and global regulatory requi...
read moreEnhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.
Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist page is loaded. Principal Regulatory Affairs Specialist.
The Senior Regulatory Affairs Specialist combines knowledge of scientific, regulatory and business issues to ensure that advertising and promotion activities meet geography specific regulatory require...
read morePrincipal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist page is loaded. Principal Regulatory Affairs Specialist.
Please be advised of the following:.The person hired for this program will be expected to relocate to manage one of our new expansion offices in the Midwest as a requirement.We are unable to consider ...
read moreSenior Regulatory Affairs Specialist. Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation update...
read moreThe Senior Regulatory Affairs Specialist combines knowledge of scientific, regulatory and business issues to ensure that advertising and promotion activities meet geography specific regulatory require...
read moreSenior Regulatory Affairs Specialist. Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation update...
read moreEnhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.
Gather and analyze the necessary data to ensure compliance with domestic (FEMA GRAS, FDA) and international (Health Canada, JECFA, GCC, Mercosur) regulatory requirements for flavors and finished goods...
read moreThe position of **Regulatory Affairs Specialist I** is within our Infectious Disease Developed Markets business unit. Prepares and Submits Regulatory Reports for FDA and other OUS (Outside of US) Re...
read moreThe position of **Regulatory Affairs Specialist I** is within our Infectious Disease Developed Markets business unit. Prepares and Submits Regulatory Reports for FDA and other OUS (Outside of US) Re...
read moreGather and analyze the necessary data to ensure compliance with domestic (FEMA GRAS, FDA) and international (Health Canada, JECFA, GCC, Mercosur) regulatory requirements for flavors and finished goods...
read moreWe are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, or a related field. Maintain an...
read moreWe are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, or a related field. Maintain an...
read moreThis is a direct hire position.Position is responsible for driving a box truck delivering furniture / displays and doing installations at the events.Duties also include loading and unloading merchandi...
read moreVaco Boston has partnered with our client to hire a Trade Compliance Analyst to join their team!.Candidates must have experience with HTS US and classification of products/parts.When: Immediate need, ...
read moreThis is a direct hire position.Position is responsible for driving a box truck delivering furniture / displays and doing installations at the events.Duties also include loading and unloading merchandi...
read moreVaco Boston has partnered with our client to hire a Trade Compliance Analyst to join their team!.Candidates must have experience with HTS US and classification of products/parts.When: Immediate need, ...
read morePosition responsibilities: .The primary duty of the CDL Class A Driver entails the safe and professional operation of a commercial motor vehicle, company equipment, and the courteous delivery of produ...
read moreSenior Regulatory Affairs Specialist/Medical Writer. Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional...
read moreSenior Regulatory Affairs Specialist/Medical Writer. Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional...
read moreActs as core team member providing review and analysis of applicable regulatory guidelines and project regulatory assessments as needed. Reviews and evaluates communications to ensure communications c...
read moreActs as core team member providing review and analysis of applicable regulatory guidelines and project regulatory assessments as needed. Reviews and evaluates communications to ensure communications c...
read moreWhich includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as re...
read moreWhich includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as re...
read moreTitle: Regulatory Affairs Ops Specialist I. Creating timelines for regulatory filings. Identifying and assessing regulatory risks and risks to timelines.
Title: Regulatory Affairs Ops Specialist I. Provide regulatory representation on key meetings, including meetings with health agency. Solid understanding and experience and interpretation of regulator...
read moreTitle: Regulatory Affairs Ops Specialist II. Lead or represent Regulatory Affairs in project teams. Compile and submit, in a timely manner, regulatory documents according to regulatory requirements.
Title: Regulatory Affairs Ops Specialist II. Lead or represent Regulatory Affairs in project teams. Compile and submit, in a timely manner, regulatory documents according to regulatory requirements.