International Regulatory Affairs Specialist

We are currently seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be pivotal in ensuring compliance with regulatory requirements for our pharmaceutical and cosmetic products. Your responsibilities will include preparing and submitting regulatory documents, coordinating...

Overview: Undergraduate or Graduate student in a Science discipline. This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group. He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects....

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, 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...

Overview: Undergraduate or Graduate student in a Science discipline.  This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group.  He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects. ...

Responsibilities: Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products' registration. Participate on product development teams, providing regulatory strategies, timelines, and direction. Reviews and approves technical documentation....

DivIHN (pronounced "divine") is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to...

Kelly Science & Clinical is seeking a Regulatory Affairs Ops Specialist near Round Lake, IL. Long term contract = ~1 year contract Shift: Monday - Friday 1st Hybrid - 3 days onsite, 2 remote Compensation: based on experience Responsibilities: Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic...

Regulatory Affairs Associate – Abbott Park, IL Must be able to work on a W2Job Summary: As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual may execute tasks and exercise influence generally at...

Regulatory Affairs Associate – Abbott Park, IL Must be able to work on a W2Job Summary: As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual may execute tasks and exercise influence generally at...

Kelly Science & Clinical is seeking a Regulatory Affairs Ops Specialist near Round Lake, IL.Long term contract = ~1 year contract Shift: Monday - Friday 1stHybrid - 3 days onsite, 2 remoteCompensation: based on experience Responsibilities:Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission...

Kelly Science & Clinical is seeking a Regulatory Affairs Ops Specialist near Round Lake, IL.Long term contract = ~1 year contract Shift: Monday - Friday 1stHybrid - 3 days onsite, 2 remoteCompensation: based on experience Responsibilities:Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission...

Work Shift:DAYWork Schedule:Why Merit?At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.ESSENTIAL FUNCTIONS PERFORMED...

Job Title: Regulatory Specialist II Duration: 12 Months (Possibility of extension) Location: Lake forest, IL (60045) - Open for remote Shift: 8 am - 5 pm Summary: The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. In this role you will prepare documentation for EU Technical Files and international product...

Title: Regulatory Specialist - Onsite Description: Years Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function Skills: Knowledge of regulations and standards affecting IVDs and/or biologics Education: BS preferred in a technical...

Regulatory Affairs Associate JR – Lake Forest, IL MUST BE ABLE TO WORK ON A W2Job Title: Regulatory Affairs Associate JRJob Summary: The Regulatory Affairs Associate Jr. supports the execution of External Regulations Standards and Guidance Documents packages by tracking and monitoring ePAS packages from draft to final closure. This role prepares metrics...

Regulatory Affairs Associate JR – Lake Forest, IL MUST BE ABLE TO WORK ON A W2Job Title: Regulatory Affairs Associate JRJob Summary: The Regulatory Affairs Associate Jr. supports the execution of External Regulations Standards and Guidance Documents packages by tracking and monitoring ePAS packages from draft to final closure. This role prepares metrics...

Regulatory Affairs Associate JR – Lake Forest, IL MUST BE ABLE TO WORK ON A W2Job Title: Regulatory Affairs Associate JRJob Summary: The Regulatory Affairs Associate Jr. supports the execution of External Regulations Standards and Guidance Documents packages by tracking and monitoring ePAS packages from draft to final closure. This role prepares metrics...

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter’s products and therapies are found in...

Job DescriptionJob Description·         The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit.  ·         In this role you will prepare documentation for EU Technical Files and international product registrations.  ·         This job description will be reviewed periodically and is...