. A Day in the Life Regulatory Affairs Specialist In this exciting role as a Regulatory Affair Specialist... – Times will be required to be work in US EST time zone. Nice to Have US and global regulatory affairs knowledge...
coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits... changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. Monitors and improves...
to medical writing and information deliverables services to leadership Regulatory Technical Communications Creates, reviews..., legal, and regulatory requirements. Monitors changes in labeling regulations in the US and/or abroad. Reviews promotional...
, Medical Affairs, Medical Information, and Drug Development by delivering timely, relevant, and high-quality insights. Leverage... and technical content, and support regulatory submissions, health agency requests, and formulary reviews. Collaborate globally...
, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM... a dynamic and experienced Specialist in Process Engineering in Active Pharmaceutical Ingredient (API) development with proven...
, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM... and analytical Specialist Quality by Design (QbD) to join our team in Hyderabad, India. In this role, you will be responsible...
, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM... and analytical Specialist Quality by Design (QbD) to join our team in Hyderabad, India. In this role, you will be responsible...
Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging... a dynamic and experienced Specialist in Formulation Development team to develop the product formulation, ensure successful pilot...
, including drug discovery, preclinical and clinical trials, regulatory affairs, pharmacovigilance, technical operations..., and integrated into workflows across the E2E value chain, from lab to market. Regulatory & Ethical Compliance: Ensure...
around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs...