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Showing posts with the label CMC Regulatory Affairs

Cadila Pharmaceuticals QA Virtual Drive 2026 for B.Pharm, M.Pharm, M.Sc & MCA | IPQA, Market Complaint, Process Validation & CSV-IT Jobs

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Cadila Pharmaceuticals Hiring for Quality Assurance Positions | Virtual Drive for IPQA, Market Complaint, Process Validation & CSV-IT (Cadila Pharmaceuticals QA Virtual Drive 2026) Introduction Cadila Pharmaceuticals Ltd. has announced a major virtual recruitment drive for experienced pharmaceutical professionals looking to build a successful career in Quality Assurance (QA). The company is hiring for multiple positions across IPQA, Market Complaint, TTD, Process Validation, and CSV-IT functions at its Dholka manufacturing facility near Ahmedabad, Gujarat. This hiring drive offers excellent opportunities for candidates with formulation manufacturing experience who want to work with one of India's well-established pharmaceutical organizations. Professionals holding B.Pharm, M.Pharm, M.Sc, or MCA qualifications can apply based on the eligibility criteria specified for each position. The interview process will be conducted virtually through Google Meet, making it convenient fo...

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Parexel Hiring Regulatory Affairs Associate in India | Hyderabad, Bengaluru & Remote Opportunities for Regulatory Professionals

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Parexel Hiring Regulatory Affairs Associate in India | Hyderabad, Bengaluru & Remote Opportunities (Parexel Hiring Regulatory Affairs Associate in India) Introduction Regulatory Affairs continues to be one of the most important and rapidly growing functions within the pharmaceutical and life sciences industry. Professionals with expertise in regulatory submissions, CMC documentation, lifecycle management, and global regulatory compliance are increasingly in demand across pharmaceutical companies, CROs, and biotechnology organizations. Parexel, a globally recognized clinical research and regulatory consulting organization, has announced a new opportunity for the position of Regulatory Affairs Associate in India. The role is available in Hyderabad, Bengaluru, and remote work locations, offering experienced regulatory professionals an opportunity to contribute to post-approval regulatory activities, CMC lifecycle management, regulatory impact assessments, and European regulatory pr...

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