Regulatory Affairs Associate - North Chicago

The Regulatory Affairs Associate will combine regulatory, business, and scientific knowledge to provide support with regulatory submissions, agency responses and internal queries for AbbVie global product portfolio. · ...

About this job: Regulatory Affairs Associate at Collabera in North Chicago, IL. · ...

Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR) and provides regulatory support for diagnostic product development and commercial diagnostic products. · ...

+The Regulatory Affairs Manager (CMC) position is responsible for the author review preparation and manage on-time filing of high-quality regulatory submissions and for post-approval maintenance of regulatory dossiers with an emphasis on CMC. · +* Authoring reviewing and preparin ...

+Job Summary · Support Publishing Operations function in Regulatory Affairs. · +Responsibilities · ensure compliance with FDA regulations. · +, An individual must assimilate to changing environments. · ...

The Regulatory Affairs Senior Associate is responsible for providing effective support to the Publishing Operations function in Regulatory Affairs. · Full-time · Description · About Meitheal · Founded in 2017 and based in Chicago, Meitheal is focused on the development and commer ...

The Senior Associate Regulatory Affairs role at Meitheal provides support to the Publishing Operations function. · The responsibilities include utilizing publishing systems for high-quality submission dossiers,ensuring compliance with FDA regulations and internal policies/procedu ...

The Griffin Museum of Science and Industry (GMSI) seeks an Associate Vice President for External Affairs to advance philanthropic vision. · Strategic leadership for stewardship engagement special events development operations membership programs. · ...

The Associate Director of CMC Regulatory Affairs will be responsible for creating CMC regulatory development plans and for successful execution against those plans. · The position requires a minimum of three days per week on-site in Xeris' Chicago office with periodic evening and ...

The Associate Director of CMC Regulatory Affairs will be responsible for creating CMC regulatory development plans and for successful execution against those plans. · The role represents the function on departmental and cross-functional initiatives. The Associate Director must be ...

We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products.This role will assist in executing global regulatory strategies, · preparing and maintaining registration dossiers, · and ensuring compliance with FDA,EU,an ...

We are seeking an experienced Regulatory Affairs Associate II to join our team. The successful candidate will have direct medical device regulatory experience with recent hands-on EU MDR 2017/745 experience. · ...

This position is primarily onsite but offers a hybrid schedule after three months with two days from home · Prepare and organize documentation for domestic and international regulatory submissions to support product approvals. · Maintain regulatory files and databases, and update ...

This role will give you hands-on experience with global regulatory processes while supporting product compliance and registration activities as part of a collaborative Regulatory Affairs team. · Prepare and organize documentation for domestic and international regulatory submissi ...

+Join our collaborative team dedicated to quality and innovation in dental medical devices. You'll gain hands-on experience in product registration and compliance while working in a supportive environment that values learning, growth, · and making an impact in a global industry. ...

Provide regulatory support and expertise associated with US and global submission requirements. · ...

Join our collaborative team dedicated to quality and innovation in dental medical devices. You'll gain hands-on experience in product registration and compliance while working in a supportive environment that values learning, growth, and making an impact in a global industry. · ...

Provide regulatory support and expertise associated with US and global submission requirements. · ...

Ready to launch your career in Regulatory Affairs? Join our collaborative team dedicated to quality and innovation in dental medical devices. You'll gain hands-on experience in product registration and compliance while working in a supportive environment that values learning, gro ...

The job is to work as a Regulatory Affairs Associate II in Lake Forest, IL 60045 for 12 months. The job requires a Bachelor's Degree preferably in pharmacy or related subject and RAC Certification. · Proven strong understanding of FDA and worldwide submission requirements. · Prep ...

We're seeking a detail-oriented Regulatory Associate who's passionate about the food industry and ready to play a key role in ensuring our products meet the highest regulatory and customer standards. · ...