Executive Regulatory Affairs Pharmaceutical

This role involves ensuring the preparation and review of regulatory documents to guarantee compliance with international guidelines and country-specific requirements.Key responsibilities include:Screening and analyzing documents for product registration requests according to country-specific guidelines.Preparing, compiling, and reviewing product dossiers in...

Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines becauseGood Health Can't Wait.We started in 1984 with a modest investment, 20 employees and a bold...

**Responsibilities**: Drug Approval, Drug related documentations,Product permission,Drug Control Visit,Making Dossier, Conduct of clinical studies, data collection, To give strategic and technical advice to R&D, production, QC department, etc right from the beginning of the development of the product, advise scientists and manufacturers on regulatory...

JD's : Regulatory Strategy: ROW Market Expansion,CTD/eCTD Dossiers,Registrations,Renewals,Variations,CDSCO Compliance & Audits: Regulatory Audits,Inspections,Artwork Compliance,Promotional Materials,Risk Mitigation Mail- Annual bonus

**Roles and Responsibilities** Jubilant FoodWorks is amidst transformation & expansion which will fuel the next level of growth and this creates both challenges and opportunities. While JFL is the largest QSR in the sub-continent, it is set to double in scale & size with a vision towards becoming a Multi Business, Multi Product, Multi Country...

Maintaining Quality SystemsEnsuring cGMP compliancePrepare Batch Manufacturing RecordsProcess Validation and Cleaning ValidationDossier Preparation and New Drug ApplicationsDocument Quality Risk activities Required Candidate profile Experience in GMP, ICH Q series and pharmaceutical quality systemsStrong in documentation, audit preparedness and regulatory...

Responsibilities: Develop and maintain strong relationships with KOLs, academic institutions, medical societies, and other relevant stakeholders in assigned therapeutic areas. Serve as a credible and trusted scientific resource for healthcare professionals, providing accurate and up-to-date information on our products, disease states, clinical data, and...

Job Title: Senior Pharmaceutical IT ManagerWe are seeking an experienced IT professional to lead our pharmaceutical manufacturing systems. The ideal candidate will have 6-8 years of experience in the industry, including technical and functional knowledge of MES & L2 systems.The successful candidate will ensure adherence to global regulations (FDA 21 CFR Part...

We are seeking an experienced professional to lead our sales efforts in the pharmaceutical industry. As a Territory Business Manager, you will be responsible for driving sales growth and revenue in your assigned territory.Key Responsibilities:You will conduct market research and gather intelligence on competitor activity and market trends.You will identify...

**Responsibilities and duties** **Requirements**: - Master’s Degree in Biological Science, applied biology or related field. - 3+ years’ practical experience with licenses and certification legal procedures. - Extensive background in data mining and analysis. - Able to understand various botanical and pharmacological common methods and specific...