🌟 We’re Hiring – In-Licensing Specialist | New Delhi 🌟 Do you want to join a company that is on track to become the No. 1 Oncology & Hematology company in the Philippines next year? 🚀 If yes, this is your chance. At GetMeds, we believe in more than just medicines. We believe in partnerships, innovation, and building a legacy of accessible, life-saving treatments. As we expand in India, we are looking for a passionate and experienced professional to join our In-Licensing Department in New Delhi. 🔹 Role: In-Licensing Specialist 📍 Location: New Delhi, India 💰 Salary: Up to ₹6,00,000 per annum Key Responsibilities: Identify, evaluate, and execute in-licensing opportunities with Indian pharmaceutical manufacturers. Collaborate with regulatory and R&D teams to ensure compliance for in-licensed products. Develop and manage contract manufacturing partnerships to support product pipeline expansion. Negotiate terms, agreements, and long-term collaborations with Indian pharma companies. Support cross-functional teams in new product launches for oncology and hematology portfolios. Track market trends, competitor activities, and regulatory changes impacting licensing strategies. Qualifications & Skills: ✔️ Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related fields. ✔️ 2–5 years of experience in regulatory affairs, in-licensing, business development, or contract manufacturing tie-ups within the pharmaceutical industry. ✔️ Strong understanding of the Indian pharma market and licensing processes. ✔️ Excellent negotiation, communication, and relationship management skills. ✔️ Entrepreneurial mindset with the ability to thrive in a fast-paced environment. Why Join Us? ✨ Be part of a company transforming cancer care access across Asia. ✨ Work on strategic partnerships that will shape the future of oncology and hematology medicines. ✨ Join a global team driven by purpose, growth, and impact. ✨ Opportunity to grow alongside a rapidly expanding international pharma company. 📩 How to Apply: Send your CV to: 📧 dra3@2mginc.com 📧 hr2@getmeds.ph Let’s build the future of healthcare together. 💊🌍 #Hiring #PharmaJobs #InLicensing #BusinessDevelopment #Regulatory #Oncology #Hematology #GetMeds
🌟 We’re Hiring – In-Licensing Specialist | New Delhi 🌟 Do you want to join a company that is on track to become the No. 1 Oncology & Hematology company in the Philippines next year? 🚀 If YES this is your chance. At GetMeds, we believe in more than just medicines. We believe in partnerships, innovation, and building a legacy of accessible, life-saving treatments. As we expand in India, we are looking for a passionate and experienced professional to join our In-Licensing Department in New Delhi. 🔹 Role: In-Licensing Specialist 📍 Location: New Delhi, India 💰 Salary: Up to ₹600,000 per annum Key Responsibilities: Identify, evaluate, and execute in-licensing opportunities with Indian pharmaceutical manufacturers. Collaborate with regulatory and R&D teams to ensure compliance for in-licensed products. Develop and manage contract manufacturing partnerships to support product pipeline expansion. Negotiate terms, agreements, and long-term collaborations with Indian pharma companies. Support cross-functional teams in new product launches for oncology and hematology portfolios. Track market trends, competitor activities, and regulatory changes impacting licensing strategies. Qualifications & Skills: ✔ Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related fields. ✔ 2–5 years of experience in regulatory affairs, in-licensing, business development, or contract manufacturing tie-ups within the pharmaceutical industry. ✔ Strong understanding of the Indian pharma market and licensing processes. ✔ Excellent negotiation, communication, and relationship management skills. ✔ Entrepreneurial mindset with the ability to thrive in a fast-paced environment. Why Join Us? ✨ Be part of a company transforming cancer care access across Asia. ✨ Work on strategic partnerships that will shape the future of oncology and hematology medicines. ✨ Join a global team driven by purpose, growth, and impact. ✨ Opportunity to grow alongside a rapidly expanding international pharma company. 📩 How to Apply? Send your CV to: 📧 dra3@2mginc.com 📧 hr2@getmeds.ph Let’s build the future of healthcare together. 💊🌍 #Hiring #PharmaJobs #InLicensing #BusinessDevelopment #Regulatory #Oncology #Hematology #GetMeds
🌟 We’re Hiring – In-Licensing Specialist | New Delhi 🌟 Do you want to join a company that is on track to become the No. 1 Oncology & Hematology company in the Philippines next year? 🚀 If yes, this is your chance. At GetMeds, we believe in more than just medicines. We believe in partnerships, innovation, and building a legacy of accessible, life-saving treatments. As we expand in India, we are looking for a passionate and experienced professional to join our In-Licensing Department in New Delhi. 🔹 Role: In-Licensing Specialist 📍 Location: New Delhi, India 💰 Salary: Up to ₹6,00,000 per annum Key Responsibilities: Identify, evaluate, and execute in-licensing opportunities with Indian pharmaceutical manufacturers. Collaborate with regulatory and R&D teams to ensure compliance for in-licensed products. Develop and manage contract manufacturing partnerships to support product pipeline expansion. Negotiate terms, agreements, and long-term collaborations with Indian pharma companies. Support cross-functional teams in new product launches for oncology and hematology portfolios. Track market trends, competitor activities, and regulatory changes impacting licensing strategies. Qualifications & Skills: ✔️ Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related fields. ✔️ 2–5 years of experience in regulatory affairs, in-licensing, business development, or contract manufacturing tie-ups within the pharmaceutical industry. ✔️ Strong understanding of the Indian pharma market and licensing processes. ✔️ Excellent negotiation, communication, and relationship management skills. ✔️ Entrepreneurial mindset with the ability to thrive in a fast-paced environment. Why Join Us? ✨ Be part of a company transforming cancer care access across Asia. ✨ Work on strategic partnerships that will shape the future of oncology and hematology medicines. ✨ Join a global team driven by purpose, growth, and impact. ✨ Opportunity to grow alongside a rapidly expanding international pharma company. 📩 How to Apply: Send your CV to: 📧 dra3@2mginc.com 📧 hr2@getmeds.ph Let’s build the future of healthcare together. 💊🌍 #Hiring #PharmaJobs #InLicensing #BusinessDevelopment #Regulatory #Oncology #Hematology #GetMeds
🌟 We’re Hiring – Business Development Specialist | New Delhi 🌟 Qualifications & Skills: ✔️ Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related fields. ✔️ 2–5 years of experience in business development roles, regulatory affairs experienceis a plus, in-licensing, or contract manufacturing tie-ups within the pharmaceutical industry. ✔️ Strong understanding of the Indian pharma market and Asean market and licensing processes. ✔️ Excellent negotiation, communication, and relationship management skills. ✔️ Entrepreneurial mindset with the ability to thrive in a fast-paced environment. Do you want to join a company that is on track to become the No. 1 Oncology & Hematology company in the Philippines next year? 🚀 If yes, this is your chance. At GetMeds, we believe in more than just medicines. We believe in partnerships, innovation, and building a legacy of accessible, life-saving treatments. As we expand in India, we are looking for a passionate and experienced professional to join our In-Licensing Department in New Delhi. 🔹 Role: Business Development Specialist 📍 Location: New Delhi, India 💰 Salary: Up to ₹6,00,000 per annum Key Responsibilities: Identify, evaluate, and execute in-licensing opportunities with Indian pharmaceutical manufacturers. Collaborate with regulatory and R&D teams to ensure compliance for in-licensed products. Develop and manage contract manufacturing partnerships to support product pipeline expansion. Negotiate terms, agreements, and long-term collaborations with Indian pharma companies. Support cross-functional teams in new product launches for oncology and hematology portfolios. Track market trends, competitor activities, and regulatory changes impacting licensing strategies. Why Join Us? ✨ Be part of a company transforming cancer care access across Asia. ✨ Work on strategic partnerships that will shape the future of oncology and hematology medicines. ✨ Join a global team driven by purpose, growth, and impact. ✨ Opportunity to grow alongside a rapidly expanding international pharma company. 📩 How to Apply: Send your CV to: 📧 dra3@2mginc.com 📧 hr2@getmeds.ph Let’s build the future of healthcare together. 💊🌍 #Hiring #PharmaJobs #InLicensing #BusinessDevelopment #Regulatory #Oncology #Hematology #GetMeds
🌟 We’re Hiring – Business Development/In-Licensing Specialist | New Delhi 🌟 Do you want to join a company that is on track to become the No. 1 Oncology & Hematology company in the Philippines next year? 🚀 If YES this is your chance. At GetMeds, we believe in more than just medicines. We believe in partnerships, innovation, and building a legacy of accessible, life-saving treatments. As we expand in India, we are looking for a passionate and experienced professional to join our In-Licensing Department in New Delhi. 🔹 Role: Business Development/In-licensing Specialist 📍 Location: New Delhi, India 💰 Salary: Up to ₹600,000 per annum 📌 Requirement: Minimum 2 years of proven experience in in-licensing, business development, regulatory affairs, or contract manufacturing tie-ups within the pharmaceutical industry. Key Responsibilities: Identify, evaluate, and execute in-licensing opportunities with Indian pharmaceutical manufacturers. Collaborate with regulatory and R&D teams to ensure compliance for in-licensed products. Develop and manage contract manufacturing partnerships to support product pipeline expansion. Negotiate terms, agreements, and long-term collaborations with Indian pharma companies. Support cross-functional teams in new product launches for oncology and hematology portfolios. Track market trends, competitor activities, and regulatory changes impacting licensing strategies. Qualifications & Skills: ✔ Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related fields. ✔ Minimum 2–5 years of relevant industry experience ✔ Strong understanding of the Indian pharma market and licensing processes. ✔ Excellent negotiation, communication, and relationship management skills. ✔ Entrepreneurial mindset with the ability to thrive in a fast-paced environment. Why Join Us? ✨ Be part of a company transforming cancer care access across Asia. ✨ Work on strategic partnerships that will shape the future of oncology and hematology medicines. ✨ Join a global team driven by purpose, growth, and impact. ✨ Opportunity to grow alongside a rapidly expanding international pharma company. 📩 How to Apply? Send your CV to: 📧 dra3@2mginc.com 📧 hr2@getmeds.ph Let’s build the future of healthcare together. 💊🌍 #Hiring #PharmaJobs #InLicensing #BusinessDevelopment #Regulatory #Oncology #Hematology #GetMeds
Company Description Getmeds, established in 2020, is a multinational pharmaceutical company with a diverse portfolio in Oncology, Hematology, Anesthesiology, and rare diseases. The company has rapidly gained recognition in the pharmaceutical industry, earning accolades at major healthcare conventions. Getmeds is dedicated to driving innovation and improving the lives of millions of patients in the Philippines. With ongoing expansion into India, Singapore, Vietnam, and other regions, Getmeds aims to make a significant global impact on healthcare. We’re Expanding Our Global Team! Are you a bidding expert with a proven track record of winning international health tenders? We’re searching for a results-driven professional who thrives in high-stakes, competitive procurement environments. What you’ll bring: 1. Demonstrated success securing bids with major global health procurement agencies and multilateral organizations. 2. Deep knowledge of international tendering frameworks, compliance standards, and donor-funded health projects. 3. A strong global network across donor agencies, NGOs, and procurement bodies. 4. End-to-end expertise in the bid cycle: opportunity tracking, proposal development, pricing strategy, and negotiations. 5. A winner’s mindset driven by results, growth, and lasting impact. Job Qualification; Bachelor’s degree in Business Administration, International Relations, Public Health, or a related field (Master’s degree is an advantage). Proven track record of successfully winning international health tenders with donor agencies, NGOs, and multilateral organizations. Strong knowledge of international tendering frameworks, compliance standards, and donor-funded project requirements. Established global network across donor agencies, NGOs, and health procurement bodies. End-to-end expertise in the bid cycle: opportunity tracking, proposal preparation, pricing strategy, and contract negotiations. Excellent communication, negotiation, and stakeholder management skills. Ability to thrive in high-pressure, deadline-driven, and competitive procurement environments. Strong analytical, problem-solving, and project management skills.
As an In-Licensing Specialist at GetMeds in New Delhi, you will play a crucial role in identifying, evaluating, and executing in-licensing opportunities with Indian pharmaceutical manufacturers. Your responsibilities will include collaborating with regulatory and R&D teams to ensure compliance for in-licensed products, developing and managing contract manufacturing partnerships, negotiating agreements with Indian pharma companies, and supporting cross-functional teams in new product launches for oncology and hematology portfolios. Additionally, you will be expected to track market trends, competitor activities, and regulatory changes impacting licensing strategies. Qualifications & Skills: - Bachelors or Masters degree in Pharmacy, Life Sciences, or related fields. - 5 years of experience in regulatory affairs, in-licensing, business development, or contract manufacturing tie-ups within the pharmaceutical industry. - Strong understanding of the Indian pharma market and licensing processes. - Excellent negotiation, communication, and relationship management skills. - Entrepreneurial mindset with the ability to thrive in a fast-paced environment. If you join GetMeds, you will be part of a company that is transforming cancer care access across Asia. You will have the opportunity to work on strategic partnerships that will shape the future of oncology and hematology medicines. Being part of a global team driven by purpose, growth, and impact, you will have the opportunity to grow alongside a rapidly expanding international pharma company. To apply for this exciting opportunity, please send your CV to: - dra3@2mginc.com - hr2@getmeds.ph Let's build the future of healthcare together. As an In-Licensing Specialist at GetMeds in New Delhi, you will play a crucial role in identifying, evaluating, and executing in-licensing opportunities with Indian pharmaceutical manufacturers. Your responsibilities will include collaborating with regulatory and R&D teams to ensure compliance for in-licensed products, developing and managing contract manufacturing partnerships, negotiating agreements with Indian pharma companies, and supporting cross-functional teams in new product launches for oncology and hematology portfolios. Additionally, you will be expected to track market trends, competitor activities, and regulatory changes impacting licensing strategies. Qualifications & Skills: - Bachelors or Masters degree in Pharmacy, Life Sciences, or related fields. - 5 years of experience in regulatory affairs, in-licensing, business development, or contract manufacturing tie-ups within the pharmaceutical industry. - Strong understanding of the Indian pharma market and licensing processes. - Excellent negotiation, communication, and relationship management skills. - Entrepreneurial mindset with the ability to thrive in a fast-paced environment. If you join GetMeds, you will be part of a company that is transforming cancer care access across Asia. You will have the opportunity to work on strategic partnerships that will shape the future of oncology and hematology medicines. Being part of a global team driven by purpose, growth, and impact, you will have the opportunity to grow alongside a rapidly expanding international pharma company. To apply for this exciting opportunity, please send your CV to: - dra3@2mginc.com - hr2@getmeds.ph Let's build the future of healthcare together.
Qualifications: ✔ Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related fields. ✔ 3–5 years of experience in regulatory affairs, or contract manufacturing tie-ups within the pharmaceutical industry. ✔ Strong understanding of the Indian pharma market and licensing processes. ✔ Excellent negotiation, communication, and relationship management skills. ✔ Entrepreneurial mindset with the ability to thrive in a fast-paced environment. Key Responsibilities: - Prepare, review, and submit regulatory dossiers (CTD/eCTD/ACTD) for product registration, variations, and renewals to the Food and Drug Administration (FDA/ other global authorities). - Ensure dossiers contain accurate CMC, non-clinical, and clinical data as required by each market. - Review, prepare Non-Clinical and Clinical Data, Risk Management Plan (RMP), Periodic Safety Update Report (PSUR) - Ensure compliance with national and international regulatory requirements, guidelines, and timelines. - Coordinate with cross-functional teams (R&D, QA, QC, Manufacturing, Marketing) to gather and verify technical documents needed for submissions. - Coordinate with API vendors for DMFs, technical queries, and COAs. - Coordinate with the BE/CDP centers - Support manufacturing sites during audits, inspections, and GMP compliance activities. - Ensure compliance with local and international GMP regulatory requirements - Provide regulatory support for product launches. - Monitor changes in regulatory guidelines and communicate updates to management and relevant departments. - Keep proper records of submissions, approvals, and correspondence with health authorities. - Assist in developing regulatory strategies for new products or markets. - Support pharmacovigilance and post-marketing surveillance requirements as needed. Skills and Knowledge: - Strong understanding of global regulatory requirements (USFDA, EMA, MHRA, TGA, Health Canada, CDSCO – India, ASEAN, WHO). - Experience in preparation, review, and submission of regulatory dossiers (DMF, ANDA, NDA, MAA, CTD/eCTD). - Knowledge of variations, renewals, post-approval changes. - Familiarity with ICH, GxP, and pharmacovigilance regulations. - Good communication and scientific writing skills. - Proficiency in MS Office, regulatory submission tools/software. Other Requirements: * Attention to detail and accuracy in documentation. * Strong organizational and project management skills. * Ability to coordinate with R&D, QA, QC, and manufacturing teams. * Stay updated with global regulatory changes (ASEAN, CIS, EAEU, USFDA, EU, GCC, WHO, etc.). * Prepare regulatory strategies for new product development. * Communicate with clients, partners, and manufacturers regarding regulatory requirements. Please send your resume to : hr2@getmeds.ph; hr@getmeds.ph; dra2@2mginc.com
🚀 We’re Hiring: Regulatory Affairs Manager / Senior Regulatory Affairs Executive Location: India (Hybrid / On-site) Industry: Pharmaceutical & Life Sciences Experience Level: Mid–Senior (3–5 years) Are you a regulatory professional who thrives at the intersection of science, strategy, and execution? We’re looking for a driven Regulatory Affairs leader to help shape and expand pharmaceutical products across India and global markets. This role is ideal for someone with a strong regulatory foundation, commercial awareness, and an entrepreneurial mindset. 🔍 What You’ll Do As a key member of our regulatory team, you will play a critical role in product development, registration, and lifecycle management across multiple markets. Regulatory Submissions & Compliance Prepare, review, and submit regulatory dossiers (CTD/eCTD/ACTD) for product registration, variations, and renewals to FDA and other global health authorities. Ensure accuracy and completeness of CMC, non-clinical, and clinical documentation in line with market-specific requirements. Review and prepare Non-Clinical & Clinical Data, including RMPs, PSURs, and post-approval documentation. Maintain full compliance with national and international regulatory guidelines, timelines, and best practices. Cross-Functional & External Coordination Collaborate closely with R&D, QA, QC, Manufacturing, and Marketing teams to gather, verify, and align technical documentation. Coordinate with API manufacturers for DMFs, COAs, and regulatory queries. Liaise with BE/CDP centers to support bioequivalence and clinical requirements. Provide regulatory support during GMP audits, inspections, and site compliance activities. Strategy, Monitoring & Market Support Develop and execute regulatory strategies for new products and market entry. Support product launches with timely regulatory input. Monitor evolving global regulatory guidelines and proactively communicate changes to stakeholders. Maintain accurate records of submissions, approvals, and correspondence with health authorities. Support pharmacovigilance and post-marketing surveillance activities as required. 🎓 What We’re Looking Fo r Qualifications ✔ Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related field ✔ 3–5 years of experience in Regulatory Affairs and/or pharmaceutical contract manufacturing tie-ups ✔ Strong understanding of the Indian pharmaceutical market and licensing processes ✔ Proven negotiation, communication, and relationship management skills ✔ Entrepreneurial mindset with the ability to excel in a fast-paced environment Technical Skills & Knowledge Solid understanding of global regulatory frameworks (USFDA, EMA, MHRA, TGA, Health Canada, CDSCO – India, ASEAN, WHO) Hands-on experience with DMF, ANDA, NDA, MAA, CTD/eCTD submissions Knowledge of variations, renewals, and post-approval changes Familiarity with ICH, GxP, GMP, and pharmacovigilance regulations Strong scientific writing and documentation skills Proficiency in MS Office and regulatory submission tools/software 🌟 Why Join Us? Work on high-impact pharmaceutical products with global exposure Be part of a growing, agile organization that values initiative and expertise Collaborate with experienced cross-functional and international teams Opportunity to shape regulatory strategy and influence market expansion 📩 Ready to make an impact? Apply now and be part of a team driving quality, compliance, and innovation in pharmaceuticals. #Hiring #PharmaJobs #RegulatoryAffairs #Pharmacist #Regulatory #Oncology #Hematology #GetMeds