Regulatory Affairs Associate I

**Job Title: Regulatory Affairs Associate I (International Regulatory Affairs)** **Career Level - C** **Introduction to Role**: Within International Regulatory Affairs, as Regulatory professionals, we take innovative regulatory approaches to bring life-changing medicines to patients in international markets. We work across the AZ pipeline and business to...

**Job Title - CMC RA Associate I Submission Excellence & Project Management.** **CAREER LEVEL: C** **ABOUT ASTRAZENECA** AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more...

**About Us**: An established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform **- CLYZO** **Position - Regulatory Affairs Associate.** An organization with a reputed history of 10+ years in the Pharma raw material industry, dealing in excipient products is looking for Regulatory Affair Executive having...

Job Title: Regulatory Affairs Manager ICareer Level - DIntroduction to role:The Regulatory Affairs Manager I is a regulatory specialist with project management capabilities responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables, including delivery as an individual contributor, if required. The Regulatory Affairs...

**Regulatory Affairs Associate** 2 to 5 years of experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. - To provide regulatory input on procedural and CMC documentation requirements specific to as defined by Health Authorities for assigned deliverable(s) including: - Submission delivery strategy - Review of documents - Analysis of...

**_Regulatory Affairs Associate _**: **Experience: RIM**: **Relevant experience in Regulatory and should be willing to work in EU Shifts (12:00 - 9.00 PM)**: - **Experience of handling RIM tools - Veeva Vault specifically.**: - **Basic Regulatory knowledge on regulations and Health Authorities.**: - **Excellent communication skills.** **Knowledge and...

Regulatory Affairs ManagerAt Parexel, we're committed to delivering exceptional results for our clients. As a Regulatory Affairs Manager, you'll play a critical role in ensuring the success of our clinical trials.Key Responsibilities:Regulatory Submissions: Lead the preparation and submission of regulatory documents for clinical trials, ensuring compliance...

Regulatory Professional I **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department: RA Submission Systems Development** - Are you passionate about ensuring compliance and streamlining regulatory processes in the dynamic field of life sciences? Do you have a passion for regulatory affairs and a desire to shape the...

**Job Title - Associate - International CMC Regulatory Affairs** **Career Level - C** Lead the way for a new breed of solutions-oriented Regulators Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious enterprise-thinkers we proactively take a strategic approach earlier in the product lifecycle to get...

Job Title: Sr. Regulatory Affairs SpecialistYou will be an integral member of our Clinical Informatics Regulatory Affairs team, influencing and shaping the regulatory capabilities for future success of Philips.Your Key Responsibilities:Ensure safe and effective products/solutions are brought to market on time and sustained throughout their lifecycle via...

About VantiveVantive is a new company built on the legacy of Baxter, a leading healthcare company. We are on a mission to revolutionize kidney care and other vital organ support.Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for supporting all regulatory activities...

Job Title: Regulatory Affairs AssociateAbout the Role:Parexel is seeking a highly skilled Regulatory Affairs Associate to join our team. As a key member of our regulatory team, you will be responsible for handling the pre and post-approval life cycle management of Biologic products in various markets, including Regulated (EU/US/Canada) and Emerging...

Regulatory Professional I **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN- .- **Department**:RA CMC Diabetes & Obesity**About the department** - RA CMC & Device Bangalore is an integral part of RA CMC & Device and comprised of +60 experienced professionals associated with key regulatory processes covering Chemistry...

**Key Accountabilities**: **Project Administration**: - Under supervision provide basic paper and electronic publishing services including document preparation, legacy conversion, scanning, rendering, bookmarking, hyperlinking, compilation, table of contents creation, volumization, pagination, and formatting of reports and simple submissions. - Provide...

Join Parexel's Team of Regulatory Affairs ExpertsJob Description:As a Senior Regulatory Affairs Associate - Labeling, you will be responsible for ensuring compliance with key labeling regulations and guidance, including CCDS, USPI, and packaging.You will have a strong working knowledge of labeling regulations and experience in label development, research,...

Regulatory Professional I - Labelling **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN- .**Department**:RA Labelling Projects & Planning- **The position** - As a Regulatory Professional I - Labelling at Novo Nordisk, you will be responsible for the following: - Packaging Material Coordination: Collaborate with...

Regulatory Affairs SpecialistBaxter is a leading healthcare company that is on a journey to separate its ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve.We are seeking a highly skilled Regulatory Affairs...

Regulatory Affairs ManagerAt Parexel, we're driven by a shared passion for delivering exceptional results. When our values align, there's no limit to what we can achieve.10+ years of relevant experience in Clinical Trial Regulatory SubmissionsExperience in managing clinical trial studies, playing Regulatory Leads for Global trials, and exposure to the...

Job DescriptionAmazon Kuiper Services India Private Limited - Q38 is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our Global Regulatory Affairs team, you will play a critical role in enabling and protecting Kuiper's use of radio frequency spectrum and satellite orbits worldwide.About the RoleThe successful...

Regulatory Affairs SpecialistAt Parexel, we're seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for managing the regulatory life cycle of drug products, from pre-approval to post-approval. Your expertise will be essential in ensuring compliance with regional regulatory...