Jobs: regulatory affairs specialist - labeling

Hybrid - 3 days a week in office - Princeton, NJ The Associate Director of Regulatory Affairs Labeling will assist in the development of a cross-functional labeling strategy for products worldwide, including providing expert input on labeling requirements and strategic guidance during label development, facilitating cross functional labeling discussions with...

Job Title : Regulatory Affairs Specialist Shift hours : Monday - Friday 8AM To 5PM. Job Location : Valhalla, NY Pay: $28/hr Job Description: This Regulatory Affairs Specialist contractor position supports US Beverages Regulatory Affairs initiatives. The person in this position will interact with various Regulatory Leads to complete assigned projects.The...

Regulatory Affairs SpecialistThis is an exciting opportunity to join an industry leading biotech company leading. The Regulatory Affairs Specialist will be responsible for supporting In Vitro Diagnostic Regulation (IVDR) transition activities that impact products currently CE Marked under the IVD Directive. This includes preparing revision of technical files...

Regulatory Affairs SpecialistThis is an exciting opportunity to join an industry leading biotech company leading. The Regulatory Affairs Specialist will be responsible for supporting In Vitro Diagnostic Regulation (IVDR) transition activities that impact products currently CE Marked under the IVD Directive. This includes preparing revision of technical files...

**Position Title**:Regulatory Affairs Specialist **Position Type**: Regular - Full-Time **Position Location**:Oakbrook Terrace **Requisition ID**: 28326 The Regulatory Affairs Specialist is responsible for product composition and label regulatory compliance for finished goods manufactured and sold in the US and Canadian markets. The position supports...

Job Title: Regulatory Affairs Specialist Location: Des Plaines, Illinois, United States Duration: 08 Months Job Description: Description: Must have 1-2 years of experiences in Medical Device Reg Affairs Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessments Have working knowledge in US and EU medical device submissions Work...

Job Title: Regulatory Affairs SpecialistLocation: Des Plaines, Illinois, United StatesDuration: 08 MonthsJob Description:Description:Must have 1-2 years of experiences in Medical Device Reg Affairs Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessments Have working knowledge in US and EU medical device submissions Work...

Job Description Job Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

POSITION SUMMARY The primary responsibility of the Senior Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The Sr. RAS is also responsible for ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory activities required for product...

Job DescriptionJob Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

For Current Gilead Employees and Contractors: Please log onto your Internal Career Site At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies...

Senior Regulatory Affairs Specialist will beresponsible for implementing regulatory strategies, assisting with the preparation, organization, and maintenance of documentation sufficient to ensure regulatory compliance of all new and existing products. In this role, you will prepare product submissions, handle license renewals, and provide periodic updates...

Senior Regulatory Affairs Specialist will be responsible for implementing regulatory strategies, assisting with the preparation, organization, and maintenance of documentation sufficient to ensure regulatory compliance of all new and existing products. In this role, you will prepare product submissions, handle license renewals, and provide periodic updates...

Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2Job Summary We're looking for a Regulatory Specialist with 2-5 years of experience in the medical device industry. Your responsibilities include maintaining the quality system, supporting manufacturing operations, and providing regulatory guidance. Experience with international...

Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2Job Summary We're looking for a Regulatory Specialist with 2-5 years of experience in the medical device industry. Your responsibilities include maintaining the quality system, supporting manufacturing operations, and providing regulatory guidance. Experience with international...

Regulatory Affairs Specialist – Onsite in Lake Forest, ILMust be able to work W2Summary Our client, a Fortune-500 Medical Device Company, has requested that we find them a regulatory affairs specialist to provide support and ensure efficient and compliant business processes and environment. This candidate will assist in the registration of products by...

Regulatory Affairs Specialist Onsite in Lake Forest, IL Must be able to work W2 Summary Our client, a Fortune-500 Medical Device Company, has requested that we find them a regulatory affairs specialist to provide support and ensure efficient and compliant business processes and environment. This candidate will assist in the registration of products by...

Job DescriptionJob DescriptionRegulatory Affairs SpecialistThis is an exciting opportunity to join an industry leading biotech company leading. The Regulatory Affairs Specialist will be responsible for supporting In Vitro Diagnostic Regulation (IVDR) transition activities that impact products currently CE Marked under the IVD Directive. This includes...

Regulatory Affairs SpecialistThe Regulatory Affairs Specialist IV will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. They will also coordinate clinical study trials, including offsite location for trials when needed. Essential...

*Title: Regulatory Affairs Specialist **Location: Abbott Park, IL**Duration: 7 Months**Description**Main Responsibilities*• Provide regulatory input to product lifecycle planning. Assist in SOP development and review.• Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes.• Understand and...