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Showing posts with the label Bengaluru Pharma Jobs

Acme Generics Regulatory Affairs Executive Recruitment 2026 | B.Pharm M.Pharm Jobs in Ahmedabad for EU Regulatory Affairs Professionals

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Acme Generics Regulatory Affairs Executive / Senior Executive Jobs 2026 (Acme Generics Regulatory Affairs Executive Recruitment 2026) Introduction Acme Generics has announced new recruitment opportunities for Regulatory Affairs Executive and Senior Executive positions at its Ahmedabad facility. This latest pharmaceutical job opening is ideal for professionals with experience in EU Regulatory Affairs, eCTD dossier preparation, lifecycle management, pharmaceutical compliance, and regulatory submissions. Candidates looking for Regulatory Affairs jobs in Ahmedabad, EU market pharmaceutical jobs, eCTD submission careers, or international regulatory affairs opportunities can explore this opening. The company is seeking qualified professionals who can support European regulatory operations and ensure compliance with global pharmaceutical standards. About Acme Generics Acme Generics is a well-established pharmaceutical company engaged in the development, manufacturing, and marketin...

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Infosys Consulting Hiring Senior Consultant – Business Consulting (Safety) | Pharmacovigilance Jobs in Bengaluru 2026

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Pharmacovigilance Jobs in Bengaluru 2026 (Infosys Consulting Hiring Senior Consultant) Introduction Infosys Consulting has announced a new hiring opportunity for experienced Pharmacovigilance professionals in Bengaluru, Karnataka. The company is recruiting candidates for the role of Senior Consultant – Business Consulting (Safety) to support AI-driven Pharmacovigilance transformation projects for global pharmaceutical and biotechnology clients. This latest Pharmacovigilance job in Bengaluru is an excellent opportunity for professionals with expertise in drug safety operations, case processing, signal detection, regulatory compliance, AI automation, and safety technology platforms such as Argus Safety, ArisG, Veeva Safety, ANOVA, and Medidata RAVE. Candidates looking for high-paying Pharmacovigilance consulting jobs in India, AI-enabled drug safety roles, or life sciences consulting careers should explore this opportunity immediately. About Infosys Consulting Infosys Consul...

Parexel Hiring Initiation Clinical Research Associate I in Bengaluru | Clinical Research Jobs 2026

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Parexel Hiring Initiation Clinical Research Associate I in Bengaluru | Clinical Research Jobs 2026 (Parexel Hiring Initiation Clinical Research Associate I) Introduction The clinical research industry in India is expanding rapidly, creating excellent opportunities for professionals interested in clinical operations, regulatory submissions, and site start-up activities. Parexel, one of the world’s leading Clinical Research Organizations (CROs), has announced a new opening for the position of Initiation Clinical Research Associate I (iCRA) in Bengaluru, India. This role is ideal for candidates who want to build long-term careers in: Clinical trial start-up Clinical operations Regulatory affairs Site activation TMF management Global clinical research Candidates with experience in: IRB/IEC submissions CTMS systems eTMF documentation Clinical trial compliance Site management can explore this exciting opportunity with Parexel. The position offers strong career growth, global clinical tri...

Arcolab Hiring XEVMPD/PSMF Associate in Bengaluru | Pharmacovigilance Jobs India 2026

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Arcolab Hiring XEVMPD/PSMF Associate in Bengaluru | Pharmacovigilance Jobs India 2026 (Arcolab Hiring XEVMPD/PSMF Associate in Bengaluru) Introduction Professionals looking to grow their career in Pharmacovigilance (PV), Drug Safety, and Regulatory Compliance now have an excellent opportunity with Arcolab in Bengaluru. The company is hiring experienced candidates for the position of XEVMPD/PSMF Associate, focusing on global pharmacovigilance documentation, regulatory database management, and aggregate safety reporting. This role is ideal for candidates who have hands-on experience in PSMF maintenance, XEVMPD submissions, PSUR/PADER writing, and ICSR management. The opportunity provides exposure to international regulatory frameworks such as EMA and MHRA, making it highly valuable for professionals planning long-term careers in global drug safety operations. As pharmacovigilance and regulatory affairs continue to expand globally in 2026, experienced PV professionals are becoming increas...

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