Asst Manager- EM _Onsite - Gurgaon

We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. · Critically reviews documentation intended for submission to the respective agencies for internal consisten ...

We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. · Bachelor's degree in pharmacy, Life Sciences, Biotechnology, Chemistry or related scientific field. · Hand ...

+Managing overall finance functions including annual audits. · +Preparing financial reports e.g Revenue & Expense trends Working Capital sheets Cash flows Balance sheets PnLs. · Manage Accounts payables Receivables Manage Invoicing Manage GST GST returns Preparing documentation a ...

+ Manage end-to-end calendar scheduling for Directors, including internal meetings, client discussions, reviews and leadership forums. · Handle domestic and international travel arrangements including flights, hotels visas itineraries and reimbursements. ...

We are seeking an experienced and highly motivated Project Manager (Regulatory Affairs) to lead and manage regulatory projects from initiation to completion. The ideal candidate will have a deep understanding of global regulatory frameworks, · Managing overall finance functions i ...

Job Purpose · DDReg Pharma Pvt Ltd is seeking an experienced Regulatory Affairs Medical Writer responsible for drafting, reviewing, and ensuring the accuracy of scientific and regulatory documents in alignment with global standards. The role involves preparation of complex CTD mo ...

We are seeking a proactive and detail-oriented Assistant Manager – Regulatory Affairs to join our Global Regulatory team. The ideal candidate will be responsible for driving CMC documentation, regulatory submissions, and lifecycle management for the EU & UK markets ensuring compl ...

We are seeking an experienced and highly motivated Project Manager (Regulatory Affairs) to lead and manage regulatory projects from initiation to completion. · Lead and manage regulatory projects. · ...

We are seeking an experienced and highly motivated Project Manager (Regulatory Affairs) to lead and manage regulatory projects from initiation to completion, · ensuring timely and successful product registration market authorization compliance with relevant regulatory requirement ...

DDReg Pharma Pvt Ltd is seeking an experienced Regulatory Affairs Medical Writer responsible for drafting reviewing and ensuring accuracy of scientific regulatory documents in alignment with global standards. · Draft high-quality medical regulatory documents in accordance with gl ...

We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. · ...

+We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. · Bachelor's degree in pharmacy, Life Sciences, Biotechnology, Chemistry or related scientific field A mast ...

We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. · In-depth knowledge of Health Canada. · ...

We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support global regulatory submissions and lifecycle management for pharmaceutical products. The ideal candidate will have hands-on experience with CTD/eCTD documentation, regulatory compliance, and do ...

We are looking for an experienced and accomplished Senior Manager – Regulatory Affairs (CMC) with deep expertise in US and EU regulatory frameworks. The role will drive regulatory strategy, dossier submissions, and lifecycle management activities across these key markets, ensurin ...

We are seeking an experienced and accomplished Assistant Manager – Regulatory Affairs to join our Global Regulatory team.The ideal candidate will be responsible for driving CMC documentation, regulatory submissions, and lifecycle management for the EU & UK markets. · ...

We are seeking a proactive and detail-oriented Assistant Manager – Regulatory Affairs to join our Global Regulatory team.The ideal candidate will be responsible for driving CMC documentation, regulatory submissions, and lifecycle management for the EU & UK markets, ensuring compl ...

We are seeking a proactive and detail-oriented Assistant Manager – Regulatory Affairs to join our Global Regulatory team.The ideal candidate will be responsible for driving CMC documentation, regulatory submissions, and lifecycle management for the EU & UK markets, · ensuring com ...

Job Purpose · DDReg Pharma Pvt Ltd is seeking an experienced Regulatory Affairs Medical Writer responsible for drafting, reviewing, and ensuring the accuracy of scientific and regulatory documents in alignment with global standards. The role involves preparation of complex CTD mo ...