DDReg Pharma Pvt. Ltd. Jobs in India

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 ...

Job summary · We are seeking a dynamic and detail-oriented HR Recruiter/Talent Acquisition Specialist to join our team in the pharmaceutical sector. ...

+This is a full-time on-site role for a Finance and Account Manager located in Gurugram. · + · ++Oversight of financial operations including budgeting financial planning analysis and reporting · E nsure compliance with financial regulations manage accounts handle payroll and cond ...

This role oversees the preparation and submission of regulatory documents in accordance with international guidelines. · Managing a team of professionals. · Compiling electronic Common Technical Document (eCTD) or non-eCTD submissions. · ...

We're Hiring – HR Intern Are you passionate about building a career in Human Resources and eager to gain hands-on experience in the pharmaceutical/healthcare industry? This is your chance to kickstart your journey Role: HR Intern · Location: Sector 49 Gurgaon(5 days Onsite) · Ass ...

This is a full-time Assistant Manager - Regulatory Affairs - Emerging Markets role in Gurugram. The candidate will manage regulatory submissions and ensure compliance with local and international regulatory requirements. · Solid knowledge of Regulatory Affairs. · Familiarity with ...

This is a full-time Finance Executive role located in Gurgaon for managing financial statements and ensuring compliance with Goods and Services Tax (GST). · ...

Email Marketing Plan execute optimize email marketing campaigns (newsletters lead nurturing promotional outbound). Build manage email lists segmentation targeting based ICP geography buyer personas Create manage email sequences follow-ups automation workflows Monitor improve key ...

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 ...

This is a full-time role for Assistant Manager - Regulatory Affairs - Emerging Markets located in Gurugram. · ResponsibilitiesManage regulatory submissions and ensure compliance with local and international regulatory requirements. · Cordinate with internal and external stakehold ...

+Job summary · We are looking for an experienced and accomplished Senior Manager – Regulatory Affairs (CMC) with deep expertise in US and EU regulatory frameworks. · +Lead CMC review of technical documentation for regulatory filings in US and EU markets. · Develop and implement r ...

+ 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 Manager/Asst Manager- EM_ to join our team in Gurgaon, Haryana (INDIA). · The successful candidate will have a strong background in regulatory affairs and excellent technical data interpretation skills. · The ideal candidate will have a Master's degr ...

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 ...

+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 highly organized proactive and detail-oriented Executive Assistant to provide high-level administrative operational support to senior leadership. · Manage and maintain executive calendars appointments meeting schedules · Coordinate internal external meetings incl ...

We are looking for an experienced and accomplished Senior Manager – Regulatory Affairs (CMC) with deep expertise in US and EU regulatory frameworks. · Lead CMC review of technical documentation for regulatory filings in US and EU markets, including Gap Analysis and Remediation fo ...

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 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 ...

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 ...