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Onesource is Hiring: Drug Substance Quality Assurance (DS – IPQA) Specialist in Bengaluru Location: 📍 Doddaballapur, BengaluruIndustry: 🧪 Biologics | 🧬 Drug Substance ManufacturingJob Title: Drug Substance Quality Assurance (DS – IPQA) Specialist 🚀 Exciting Opportunity with Onesource! Are you a Quality Assurance professional with a passion for biologics and drug substance manufacturing? Onesource is […]
Cadila Pharmaceuticals Walk-In (Hyderabad & Multiple Locations) – Medical Representative & Retail Field Officer Cadila Pharmaceuticals, a well-respected and growing pharmaceutical company, is offering excellent career openings for Medical Representatives and Retail Field Officers across Telangana and Andhra Pradesh. We are conducting a Walk-In Interview in Hyderabad on April 22nd, 2025, for these exciting roles.
🚀 Apply Now: Project Research Scientist Vacancy at CSIR-IIIM, [April 2025] Introduction Are you a qualified pharmacy post-graduate passionate about drug delivery systems? Here’s an exciting opportunity to join the prestigious CSIR-Indian Institute of Integrative Medicine (CSIR-IIIM), Jammu as a Project Research Scientist under a groundbreaking ICMR-funded project on triple negative breast cancer therapy. Position
Promea Walk-In (Hyderabad) – HR Executive (Recruitment) Promea Therapeutics Pvt. Ltd., a growing pharmaceutical company, is conducting a Walk-In Interview in Hyderabad for a dynamic and experienced HR Executive to handle recruitment activities. If you have a passion for talent acquisition within the pharmaceutical industry, particularly with exposure to sterile injectables, we encourage you to
Micro Labs Walk-In (Bangalore) – Multiple Positions (Male Candidates Preferred) Micro Labs Ltd, a well-known pharmaceutical company, is conducting a Walk-In Interview in Bangalore on Saturday, April 19th, 2025, for various positions across our AQA, Stores, QA, Engineering, and EHS departments. We are looking for dedicated and enthusiastic individuals, ranging from freshers to experienced professionals,
Biological E. Walk-In (Shamirpet, Hyderabad) – Multiple Quality & Engineering Roles Biological E. Limited, a leading and globally recognized vaccine and pharmaceutical company, is conducting a Walk-In Interview for experienced and dynamic professionals to join our teams in Quality Assurance, Quality Control (Biologics/Vaccines), and Engineering (Injectables/Biologics). This is an excellent opportunity to be part of
Icon Hiring for Pharmacovigilance Associate/Sr PV Associate- Apply online Pharmacovigilance Associate/Sr PV Associate Chennai JR127208 Drug Safety ICON Full Service & Corporate Support Office Based About the role This vacancy has now expired. Please click here to view live vacancies. Pharmacovigilance/ Sr Pharmacovigilance Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re
🌟 Sun Pharma Job Notification 2025 – Apply Now for Senior Management & Key Pharma Roles Are you looking to advance your career in the pharmaceutical industry? Sun Pharmaceutical Industries Ltd., one of India’s largest and most respected pharma companies, has announced multiple job openings across India. This latest Sun Pharma job notification includes exciting
Abbott Hiring for Medical Advisor Post Apply Online Medical Advisor Location India – MumbaiCategory Medical and Clinical Affairs MAIN PURPOSE OF ROLE Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements. MAIN RESPONSIBILITIES As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to implementation of clinical protocols, and facilitates completion of final reports. Recruits clinical investigators and negotiates study design and costs. Responsible for directing human clinical trials, phases III & IV for company products under development. Participates in adverse event reporting and safety responsibilities monitoring. Coordinates and provides reporting information for reports submitted to the regulatory agencies. Monitors adherence to protocols and determines study completion. Coordinates and oversees investigator initiations and group studies. May participate in adverse event reporting and safety responsibilities monitoring. May act as consultant/liaison with other corporations when working under licensing agreements. QUALIFICATIONS Education Associates Degree (± 13 years) Experience/Background Minimum 1 year APPLY ONLINE To Join In Whatsapp group
