As a Senior Regulatory and Labeling Specialist at our clients company, you will play a crucial role in ensuring that finished product labels meet the strict requirements of FDA Labeling Laws and 21 CFR Regulations. Regulatory Label Development and/or Regulatory Compliance preferred. Stay up-to-date ...
Job Title: Senior Regulatory and Labeling Specialist. As a Senior Regulatory and Labeling Specialist at our clients company, you will play a crucial role in ensuring that finished product labels meet the strict requirements of FDA Labeling Laws and 21 CFR Regulations. A minimum of 5+ years of workin...
The Senior Regulatory Specialist responsible for Canadian legislation identifies, collects, and interprets science-based reports, data, and regulations in order to prepare documents for government agencies, curate lists, and develop Environment, Health, Safety, and Transportation (EHS&T) informa...
Compile regulatory documents for FDA submission (eCTD experience preferred), including: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulato...
Which 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 required, maintaining regulatory files in a format consistent with requirements as well as staying awa...
KNOWLEDGE, SKILLS, and ABILITIES Bachelors in any of the following degrees from an accredited university/college: Regulatory Science, Regulatory Compliance, Regulatory Affairs, Environmental Science, biochemistry, biological sciences, chemistry, pharmacy, pharmacology, toxicology, medicine, and engi...
The Global Regulatory Affairs Office (GRAO) is responsible for overseeing the enhancement of our risk management and controls, remediation of regulatory and audit findings and the administration of regulatory affairs, including establishing a centralized and sustainable connection point for global r...
The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips’ Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...
Which 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 required, maintaining regulatory files in a format consistent with requirements as well as staying awa...
Staff Regulatory Affairs Specialist,. Staff Regulatory Affairs Specialist. Communicate with regulatory agencies regarding pre-submission strategies/regulatory pathway development, submissions, and follow-up on submissions in review. You will research requirements (local, national, international), ap...
Regulatory Specialist to join our team and support the Flavors business in North America. In this role, you will assure compliance of Sensient Technologies products with appropriate regulations and serve as a regulatory resource to internal and external customers. Adheres to regulatory procedures to...
Review and process entry of HMDA and CRA reportable loans with 100% accuracy into Compliance CRA Wiz system following current regulatory guidelines. Then preparing a HMDA or CRA packet for all identified loans for regulatory purposes. ...
Which 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 required, maintaining regulatory files in a format consistent with requirements as well as staying awa...
If the answers to these questions were yes; then this Director Quality Assurance and Regulatory Affairs opportunity with an outstanding Medical Device organisation in Illinois might be the change you need. Ensures compliance with regulatory standards and readiness for inspections. Independently revi...
We are seeking a highly skilled Senior Quality Professional to join our team. The ideal candidate will have a robust background in quality management within the pharmaceutical, medical device, or related life sciences industries, particularly in a cGMP/GDP manufacturing environment. This role requir...
The Compliance Specialist will ensure clients and contractors are onboarded correctly and that all contracts and onboarding files are accurate. ...
Project Manager / Senior Project Manager. This position will require an understanding of various construction & project management skills; be able to oversee the day-to-day activities of multiple construction projects; ensure client satisfaction; make decision and recommendations which will impact c...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality...
Are you ready to lead regulatory strategies that will have a global impact? Join my client as a Senior Manager in Regulatory Affairs, where youll be at the forefront of innovation in the medical device industry. Manage and mentor a team of regulatory affairs professionals. Lead and shape regulatory ...
Lead Quality Assurance Specialist. The Lead Quality Assurance Specialist is the subject matter expert and will be responsible for assisting leadership with oversight of the team. The Quality Assurance Specialist will be responsible for confirming all delivery/shipping tickets and on-site orders dail...
As a Regulatory Affairs Manager for my client, you'll play a key part in shaping the future of innovative medical devices. Step into a role where your regulatory expertise will make a global impact. Drive forward the development and compliance of products at the cutting edge of technology, ensuring ...
Title: Program Manager - Vehicle Diagnostics -2 Openings. The Diagnostics Repair Strategy Program Manager focuses upfront on the New Product Development process to help drive design for diagnostics. Managing new vehicle programs to refine the diagnostic strategy. Participates in new program concept ...
Project Manager (Quality/Clinical/Regulatory Affairs). The Project Manager provides project leadership for high-visibility, highly complex compliance initiatives across multiple business units and functions around the globe. This leader works closely with the program manager and project teams to def...
The Diagnostics Repair Strategy Program Manager focuses upfront on the New Product Development process to help drive design for diagnostics. Managing new vehicle programs to define the diagnostic strategy. Participates in new program concept sheet reviews. Create diagnostic standards for future prog...
Are you ready to lead regulatory strategies that will have a global impact? Join my client as a Senior Manager in Regulatory Affairs, where you’ll be at the forefront of innovation in the medical device industry. Manage and mentor a team of regulatory affairs professionals. Lead and shape regulatory...