Regulatory Affairs Specialist

Regulatory Affairs Specialist SeniorGentiva, a leading provider of healthcare services, is seeking a highly skilled Regulatory Affairs Specialist Senior to join our team.About the RoleThis is an exciting opportunity to contribute to the development and implementation of regulatory strategies that support our company's growth and compliance with government...

Home Search Jobs Job Description Regulatory Affairs Associate Contract: North Chicago, Illinois, US Salary: $30.00 Per Hour Job Code: End Date: Job Description: Key Responsibilities:Assist in the preparation of regulatory submissions for various product categories including Food, FSMP, Enteral Nutrition, and Pharmaceuticals. Demonstrate proficiency in...

Role Overview:As an HR Compliance and Regulatory Affairs Specialist, you will play a crucial role in ensuring that our human resources practices align with current laws and regulations.Key Responsibilities:1. **Monitoring Regulatory Changes:** Proactively track shifts in the business landscape, including legislation and regulatory standards, to assess their...

Home Search Jobs Job Description Regulatory Affairs Associate Contract Type: Temporary Location: North Chicago, Illinois, US Compensation: $30.00 Per Hour Job Overview: As a Regulatory Affairs Associate, you will play a crucial role in supporting regulatory submissions for various product categories including Food, FSMP, Enteral Nutrition, and...

Home Search Jobs Job Description Regulatory Affairs Associate Contract Type: Contract Location: North Chicago, Illinois, US Compensation: $30.00 Per Hour Job Overview: Responsibilities:Assist in the preparation and submission of regulatory documents for various product categories including Food, FSMP, Enteral Nutrition, and Pharmaceuticals. Demonstrate...

Job SummaryThe Cook Group is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements for medical devices in specific markets.Key ResponsibilitiesRegulatory Liaison: Serve as a liaison on regulatory issues between the Cook...

Job SummaryThe Regulatory Affairs Coordinator is a key member of the International Regulatory Affairs Department at International Vitamin Corporation. This role is responsible for providing regulatory, technical, and administrative support to ensure compliance with international regulations and guidelines.Key ResponsibilitiesDocument Preparation and...

Job SummaryThe Senior Manager, Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) plays a critical role in ensuring the successful delivery of products to patients. This position requires a strategic thinker who can develop and implement effective CMC regulatory strategies, build strong relationships with internal and external partners, and...

Job SummaryAbbVie is seeking a highly skilled Regulatory Affairs Director to join our team. As a key member of our Regulatory Affairs department, you will be responsible for ensuring the successful execution of post-approval change objectives for marketed products.Key ResponsibilitiesProject Management: Independently manage, compile, and author CMC sections...

Job Title: Associate Regulatory Affairs Submission ManagementLocation: Lake County AP50, or Florham Park, NJDuration:12 months 7. What are the top 3-5 skills, experience or education required for this position:1. eCTD submission publishing (advertising and promotional 2253 submissions if possible)2. US regulatory FDA guidelines/CFR3. submission/regulatory...

**Job Summary**US Tech Solutions is seeking a highly skilled Associate Regulatory Affairs Submission Management to join our team. As a key member of our regulatory affairs team, you will be responsible for managing low to medium impact submission projects involving multiple cross-functional regulatory submission teams.Key Responsibilities:Manage submission...

US Tech Solutions is seeking a skilled Regulatory Affairs Submission Management professional to join our team. The ideal candidate will have experience managing low to medium impact submission projects involving multiple cross-functional regulatory submission teams. Key responsibilities include: * Collaborating with regulatory submission teams to ensure...

Job SummaryThe Senior Manager, Regulatory Affairs CMC will work closely with internal and external partners to deliver products to patients. This role will be responsible for developing and managing content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications and supplements/variations.Key...

Job Title: Regulatory Affairs AssociateLocation: RemoteDuration: 03+ monthsThis position offers the flexibility of being fully remote or hybrid.Role Overview:In this role, you will be responsible for the organization and preparation of documentation for regulatory submissions under general supervision.Assess and analyze technical and scientific data and...

Job SummaryThe Senior Manager, Regulatory Affairs CMC will lead the development and implementation of regulatory strategies to ensure compliance with global regulations and guidelines. This role will work closely with internal and external partners to deliver high-quality products to patients.Key ResponsibilitiesDevelop and implement CMC regulatory...

Job DescriptionJob Description·         What are the top 3-5 skills, experience or education required for this position:·         eCTD submission publishing (advertising and promotional 2253 submissions if possible)·         US regulatory FDA guidelines/CFR submission/regulatory project management Veeva Promomats...

Duration: 1 year Employment Type: W-2 Overview: The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines,...

Position OverviewJob Title: Regulatory Compliance SpecialistType: ContractLocation: RemoteCompensation: Competitive hourly rate Role Responsibilities:The individual in this role will play a crucial part in the Regulatory Affairs department, assisting teams in the product registration process by preparing necessary documentation for global submissions.Key...

Duration: 1 yearEmployment Type: W-2 Overview:The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.

Duration: 1 yearEmployment Type:W-2 Overview:The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines, facilitates...