Drug regulatory affairs jobs in Bangalore

 ...Regulatory Affairs Specialist Responsibilities: Prepare and submit regulatory documentation for new and existing medical products, including drugs, devices, and biologics. Stay up-to-date on ever-evolving regulatory requirements and guidelines. Liaise with regulatory... 

 ...Medical Device Regulatory Affairs Job duties of a Regulatory Affairs Specialist include:   Developing and implementing regulatory strategies for new and existing products Preparing and submitting regulatory documentation to regulatory authorities Liaising with regulatory... 

Key Accountabilities: Project Execution: Works effectively within a team environment Works within broad project guidelines as directed by the Project Lead or Technical SME With the guidance of the project Technical SME, demonstrates the ability to prioritize work ...

 ...We are hiring for dynamic individuals in Regulatory Affairs Department: Experience: 3 years up to 12 years Designation: Senior Exec / Assistant Manager / Deputy Manager Qualification: M. Sc. / M. Pharma/ B. Pharma For Below Mentioned roles: - Role 1: - API... 

 ...combination of this will lead to a truly differentiated experience for you. If this excites you, then apply below. Lead Regulatory Affairs You will be responsible for : Responsible for Regulatory intelligence dissemination and coordination, this includes -... 

 ...Associate Manager, Regulatory Affairs (CMC) at ClinChoice (View all jobs) Bangalore or Hyderabad - India ClinChoice is a global full-...  ...accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful... 

 ...stakeholders Compiling variation packages Experienced in managing, regulatory database and Trackwise. Your experience and qualifications...  .... Experience: ~2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market ~ Knowledge on... 

 ...We are hiring for Regulatory Affairs Analyst IVD Expert Your Role: The Regulatory Affairs Analyst IVD Expert supports assigned regulatory tasks related to health authority notifications submissions and registrations regarding renewals and new products. Independently... 

 ...Drug Safety Physician (DSPs) Job duties of a Drug Safety Physician include:      Reviewing and analyzing adverse event reports, clinical...  ...in ongoing safety surveillance programs Liaising with regulatory authorities   Preferred Qualifications       A medical degree... 

 ...experienced professionals associated with key regulatory processes covering CMC, Medical Device...  ...and implement regulatory strategies for Drug-Device Combination products in alignment...  ...CAPA) cases, and representing Regulatory Affairs in audits and core groups for device development... 

 ...Department: Regulatory Affairs CMC & Device Are you passionate about what you are doing? Do you want to build excellence within processes...  ...Experience in handling regulatory submissions of medical devices or drug device combination products across the globe. Experience in... 

 ...We are looking for a Director - Medical Affairs and Medical Education to join our team at...  ...business knowledge. Strong knowledge of drug development and life cycle management...  ...department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of... 

 ...purpose of Associate Manager, Global CMC Regulatory, is to work cross functionally with Elanco...  ...of registrations/approvals of new animal drugs with global regulatory agencies.  This...  ...Competencies: ~3 to 7 years in Global Regulatory Affairs ~ Strong knowledge of FDA/CVM and EMA... 

 ...right position for you. Apply now and join a growing team, working in an international environment.   The Position   A Senior Drug Safety Associate will perform initial evaluation of reported adverse events (serious and non-serious) from all sources. Perform case entry... 

 ...dedicated EU Submission Lead for Clinical Trials to join our Global Regulatory Affairs team. If you are passionate about driving change and...  ...for electronic submissions to Health Authorities including New Drug Applications and Life Cycle submissions. Working at Novo Nordisk... 

 ...Planning   Are you detail-oriented and passionate about ensuring regulatory compliance? Do you thrive in a fast-paced and global environment...  ...Coordination: Collaborate with stakeholders across Regulatory Affairs, Affiliate, Product Supply, and Marketing to plan and coordinate... 

 ...Department: Regulatory Affairs Rare Endocrine Disorders   Are you passionate about ensuring regulatory compliance for early phase products and/or managing product life cycle and amendments? Do you want to play a crucial role in keeping patients safe and ensuring Novo... 

 ...Description Department : DIT, IB & MAPA & Corp Com Location : Bangalore Can you implement, manage and drive country-wide Public Affairs strategies at central Govt. level and at state Govt. level? Do you have the interpersonal skills to navigate in a complex stakeholder... 

 ...Head of Market Access & Government Affairs (Medical Device) Our client is a leading international...  ...and legislative direction to improve the regulatory and economic environment in India....  ...attributes of the therapeutic area drugs/medical devices to external multi-stakeholders... 

 ...Functional Job Title: Officer/ Manager Reports to: AVP for Regulatory Reporting Department/ Division: Report Preparation (Liquidity & Branch Reporting Team) Basic Purpose of Job: This role will be responsible for supporting the Liquidity (viz. Liquidity Coverage...