- Henkel (Rocky Hill, CT)
- Product Safety & Regulatory Affairs Intern - Summer 2026 **_About_** **_this_** **_Position_** At Henkel, you'll be part of an organization that's ... compliance documents, including scanning and archiving materials + Support product safety and regulatory compliance by gathering and analyzing health… more
- Henkel (Rocky Hill, CT)
- Product Safety and Regulatory Affairs Intern - Summer 2026 **_About_** **_this_** **_Position_** At Henkel, you'll be part of an organization that's ... make an impact at Henkel.** **What you'll do** As a Product Safety and Regulatory Affairs Intern, you will: + Gain hands-on experience with regulatory… more
- Parexel (Hartford, CT)
- …the go-to expert for global labeling, working side-by-side with client teams across Regulatory Affairs , Technical Operations, Safety , and Commercial. You'll ... in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs , or quality. Exceptional candidates with 3+ years of… more
- Boehringer Ingelheim (Ridgefield, CT)
- …CT location* For assigned development projects and US marketed products, the Director, US Product Group Regulatory Affairs will provide expert US ... US RA on US cross-functional teams. The Director, US Product Group Regulatory Affairs will...preparation, content, and distribution in the US of critical safety or quality communications (including DHCP letters) for assigned… more
- Boehringer Ingelheim (Ridgefield, CT)
- …development requirements including preparation of documentation, as appropriate **Description** The Regulatory Affairs Product Strategy Fellowship is ... advocate to achieve common goals for assigned projects, with supervision. With supervision, the Product Group Regulatory Affairs Fellow will: + Regulatory… more
- Parexel (Hartford, CT)
- …the go-to expert for global labeling, working side-by-side with client teams across Regulatory Affairs , Technical Operations, Safety , and Commercial. You'll ... in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs , or quality. Exceptional candidates with 3+ years of… more
- Boehringer Ingelheim (Ridgefield, CT)
- …assigned assets, lead the Regulatory Excellence Team (RET) and represent Global Regulatory Affairs (GRA) on the Evidence Team. The Director, Global ... molecule) + Further degrees/certifications: Specialized Pharmacist or Master of Drug Regulatory Affairs , RAC certification Technical expertise: + In-depth… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Legal, Epidemiology & RWE, early and late-stage Clinical Development teams, Regulatory Affairs , Drug Safety , Digital). **Eligibility Requirements** ... considered a plus). + For roles in Early Medical Affairs : Track record in product launch activities... Affairs (TMMA) and collaborates cross-functionally (Clinical Development, Regulatory , Safety , Marketing, PPSS, Legal, etc.). +… more
- Boehringer Ingelheim (Ridgefield, CT)
- …(eg Epidemiology, early and late-stage Clinical Development teams, Regulatory Affairs , Drug Safety , Marketing, PPSS ( Product Pipeline Scientific ... Global Medical Advisor (GMA) is medically responsible for the product -related Medical Affairs strategy, its implementation in... specific input to global Pharmacovigilance (PV) and global Regulatory Affairs (RA). + Develops and/or provides… more
- Boehringer Ingelheim (Ridgefield, CT)
- …assigned drug responsibilities, including: + Continuous monitoring and further development of the product safety profile + Safety issue management + Set-up ... in clinical trial database + Close collaboration with Global Epidemiology and Medical Affairs on safety -focused clinical and Epidemiologic studies + Review and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …assigned drug responsibilities, including: + Continuous monitoring and further development of the product safety profile + Safety issue management + Set-up ... in clinical trial databases + Close collaboration with Global Epidemiology and Medical Affairs on safety -focused clinical and epidemiologic studies + Review and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Communications, Legal, Epidemiology & RWE, early and late-stage Clinical Development teams, Regulatory Affairs , Drug Safety , Digital). **Compensation** This ... starting at early development until the end of the product 's life cycle. + The Medical Affairs ...the product 's life cycle. + The Medical Affairs strategy related to early pipeline compounds/indication/portfolio aims to… more
- Boehringer Ingelheim (Ridgefield, CT)
- …patient safety physicians responsible for an investigational compound or product including project-specific training and coaching of team members, review of team ... to US line management, this position may matrix report to a Lead Patient Safety Physician, TA Oncology. As an employee of Boehringer Ingelheim, you will actively… more
- Medtronic (North Haven, CT)
- …medical device products (Capital and disposable). This role is pivotal in ensuring product safety , regulatory compliance, and effective risk mitigation ... + Collaborate with cross-functional teams, including R&D, manufacturing, NPD and regulatory affairs , to define and implement systems engineering processes… more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. + Provides ... the strategy for drug approval, and life cycle management to maximize a product 's full potential. There are numerous compounds currently in the pipeline. In… more
- Boehringer Ingelheim (Ridgefield, CT)
- …medical leadership in regulatory meetings and contributes to submission strategy, regulatory dossiers, safety issues. + Serves as chairperson of the ... responsibility for the projects assigned, eg definition of Target Product Profiles, Clinical Development Plan, Pediatric Investigational Plan, core Clinical… more
- Adecco US, Inc. (Southington, CT)
- …all quality, quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating procedures for ... and comfortable using computers. *Working knowledge of the medical device regulatory procedures, lean manufacturing, and manufacturing processes preferred. *Must be… more
- Contract Pharmacal Corp (Hauppauge, NY)
- …and provide information to other departments, as requested. + Coordinate with the Regulatory Affairs group to maintain and update specifications as required ... QC Manager in one of the assigned QC laboratories (Raw Material, Finished Product , Microbiology, ICP, Technical Support) with any tasks including, but not limited… more
