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Showing posts with the label Pharm D Job Opportunities India

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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“Clinical Project Associate Jobs in Mumbai | Zydus Healthcare Hiring for M.Pharm, Pharm D & MSc Graduates”

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"Clinical Project Associate Jobs in Mumbai at Zydus Healthcare – Apply Now" (Zydus Healthcare Hiring) Are you a passionate clinical research professional or fresher looking to start your career with a reputed pharmaceutical company? Zydus Healthcare Limited , one of India’s leading pharma giants, is hiring for the role of Clinical Project Associate at its Mumbai location. This position is an excellent opportunity for M.Pharm, Pharm D, and MSc Life Sciences graduates (freshers or candidates with up to 1 year of experience) who want to gain hands-on expertise in clinical research, post-marketing studies, and regulatory compliance . Job Responsibilities:- As a Clinical Project Associate at Zydus Healthcare , you will be responsible for: Supporting the Clinical Operations Manager and Medical team in planning and executing post-marketing studies. Coordinating with CROs for protocol digitization, CRF development, agreements, and informed consent forms. Tracking study p...

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