Location - Ahmedabad (Apply only Ahmedabad Based Candidates) 5 Days Working Male Candidates Preferred. Preferred Pharma Exports Accounting Experience & Knowledge. Core Accounting & Bookkeeping: o Manage all accounting transactions and maintain accurate books of accounts in Tally Prime. o Handle day-to-day entries for sales, purchases, expenses, and journal vouchers. o Perform monthly closing activities, including ledger scrutiny, and prepare trial balances. o Manage accounts payable and receivable, ensuring timely processing of payments and collections. o Conduct regular bank reconciliations for all domestic and foreign currency accounts. Export Finance & Compliance: o Manage all financial aspects of export transactions, including the preparation and verification of export invoices against purchase orders and L/C terms. o Liaise with banks for the submission and negotiation of export documents under Letters of Credit (L/C), CAD, D/P, etc. o Track foreign currency remittances and ensure timely issuance of Bank Realization Certificates (BRC/e-BRC). Account for foreign exchange fluctuations, including calculating and booking exchange gains or losses. o Prepare documentation for and file GST (IGST) refund claims and Duty Drawback claims. Taxation & Statutory Compliance: o Ensure timely calculation and deposit of statutory dues, including GST, TDS, and Professional Tax. o Prepare and file monthly, quarterly, and annual GST returns (GSTR-1, GSTR-3B). o Perform regular reconciliation of GST data, including GSTR-2A/2B reconciliation. o Assist in the preparation of data for income tax assessments and statutory audits. o Ensure compliance with FEMA regulations related to export transactions. Financial Reporting & MIS: o Assist in the finalization of accounts and the preparation of financial statements (Profit & Loss, Balance Sheet). o Prepare and maintain financial MIS reports for management review. o Provide data and support for budgeting and financial forecasting activities. Qualifications and Skills: Education: Bachelor’s degree in Commerce (B.Com) or Master's degree in Commerce (M.Com). Candidates who have completed CA Intermediate are highly encouraged to apply. Experience: A minimum of 3-4 years of relevant accounting experience. Prior experience working with a merchant exporter is mandatory. Experience in the pharmaceutical or chemical industry is a significant advantage. • Technical Skills: o Expert proficiency in Tally Prime is essential. o Advanced skills in MS Excel, including VLOOKUP, HLOOKUP, PivotTables, and other functions. o Hands-on experience with online banking portals for domestic and international transactions. o Familiarity with the GST portal and other government compliance portals. Knowledge: o Strong understanding of Indian Accounting Standards. o In-depth knowledge of GST rules, TDS provisions, and customs regulations related to exports. o Solid understanding of FEMA guidelines and export finance documentation (L/C, BRC, etc.). Job Types: Full-time, Contractual / Temporary Pay: From ₹22,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Work Location: In person
Job location - Ahmedabad Gujarat. Experience Required - 03 to 5 Years in Pellets Pharma Industry Job Role - International Sales Manager - Pellets Products Job Role Summary - I nternational Sales Manager / Executive will drive global export growth by identifying new markets, onboarding distributors, and managing key client relationships. Roles And Responsibilities - - Develop and execute sales plans aligned with company export objectives - Good International contacts or have developed in international clients. - Generate and convert leads—prepare proposals, negotiate pricing, MOQs, Incoterms, and contractual terms. - Identify the countries and Potential Markets. - Understanding of pharmaceutical export documentation (COPP, CoA, FSSAI, etc.). - Ability to align with Pellets Pharma’s vision and values Skills Required - - B.Pharm / M.Pharm / B.Sc. in life sciences, or MBA in Marketing / International Business preferred. - 3–7 years in pharma export or international sales (Preferred Pharma manufacturing) - Strong negotiation and communication skills. - Ready to International Business Travelling - Salary Range - 5 L to 7 L Benefits - - Provide Medical insurance - Paid Leaves and Sick Leaves - Yearly Bonus and Yearly Increment - Working 5 Days - Other benefits Job Type: Full-time Pay: From ₹500,000.00 per year Benefits: Cell phone reimbursement Health insurance Paid sick time Paid time off Provident Fund Work Location: In person
Job location - Ahmedabad Gujarat. Experience Required - 03 to 5 Years in Pellets Pharma Industry Job Role - International Sales Manager - Pellets Products Job Role Summary - I nternational Sales Manager / Executive will drive global export growth by identifying new markets, onboarding distributors, and managing key client relationships. Roles And Responsibilities - - Develop and execute sales plans aligned with company export objectives - Good International contacts or have developed in international clients. - Generate and convert leads—prepare proposals, negotiate pricing, MOQs, Incoterms, and contractual terms. - Identify the countries and Potential Markets. - Understanding of pharmaceutical export documentation (COPP, CoA, FSSAI, etc.). - Ability to align with Pellets Pharma’s vision and values Skills Required - - B.Pharm / M.Pharm / B.Sc. in life sciences, or MBA in Marketing / International Business preferred. - 3–7 years in pharma export or international sales (Preferred Pharma manufacturing) - Strong negotiation and communication skills. - Ready to International Business Travelling - Salary Range - 5 L to 7 L Benefits - - Provide Medical insurance - Paid Leaves and Sick Leaves - Yearly Bonus and Yearly Increment - Working 5 Days - Other benefits Job Type: Full-time Pay: From ₹500,000.00 per year Benefits: Cell phone reimbursement Health insurance Paid sick time Paid time off Provident Fund Work Location: In person
Job Title: Jr. Regulatory Affairs (Semi-Regulated Markets) Company: GenAide Pharmaceutical Pvt Ltd Location: 909, Satyamev Eminence, Science City Road, Near Shukan Mall, Sola, Ahmedabad, Gujarat 380060 About GenAide Pharmaceutical Pvt Ltd: GenAide Pharmaceutical Pvt Ltd is a young, energetic, and rapidly growing pharmaceutical company committed to delivering high-quality healthcare products. We foster a dynamic work environment with a strong emphasis on teamwork and innovation. Join our already developed team and contribute to our exciting journey! Job Type: Full-time Working Days: Monday to Friday (5-day work week) Salary: INR 150000 - INR 300000 per annum Experience: 01-02 years in Regulatory Affairs, with a strong focus on semi-regulated markets. Job Summary: GenAide Pharmaceutical Pvt Ltd is seeking an experienced and highly motivated Regulatory In-charge to lead our regulatory team for semi-regulated markets. The ideal candidate will be responsible for overseeing all regulatory activities, ensuring compliance with local and international regulations, and facilitating timely product registrations in these key regions. This leadership role requires a proactive approach, excellent communication skills, and a deep understanding of regulatory pathways in diverse semi-regulated environments. Key Responsibilities: Regulatory Strategy & Planning: Develop and implement effective regulatory strategies for product registration, lifecycle management, and post-market surveillance in semi-regulated markets. Dossier Preparation & Submission: Oversee the preparation, compilation, and submission of high-quality regulatory dossiers (e.g., CTD, ACTD, country-specific formats) to health authorities in semi-regulated countries. Team Leadership & Mentorship: Lead, mentor, and guide a team of regulatory professionals, fostering a collaborative and high-performance environment. Provide technical expertise and support to the team. Compliance & Due Diligence: Ensure all regulatory activities comply with applicable national and international guidelines, Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs). Conduct regulatory intelligence and assess the impact of new regulations. Health Authority Liaison: Act as the primary point of contact with regulatory agencies in semi-regulated markets, managing queries, providing responses, and facilitating approvals. Artwork & Labeling Review: Review and approve product artworks, labeling, and promotional materials for compliance with regulatory requirements. Post-Approval Variations: Manage and submit post-approval variations, renewals, and other lifecycle management activities for registered products. Cross-functional Collaboration: Collaborate effectively with internal departments such as R&D, Quality Assurance, Production, Sales, and Marketing to ensure regulatory requirements are integrated into business processes. Documentation & Record Keeping: Maintain accurate and up-to-date regulatory documentation and databases. Qualifications: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related scientific discipline. 1-2 years of progressive experience in Regulatory Affairs within the pharmaceutical industry, specifically with a strong track record in semi-regulated markets. In-depth knowledge of regulatory guidelines and requirements for various semi-regulated countries (e.g., ASEAN, LATAM, Africa, CIS regions, etc.). Proven experience in leading and managing a regulatory team. Excellent understanding of dossier requirements (e.g., CTD/ACTD structure). Strong analytical, problem-solving, and decision-making skills. Exceptional written and verbal communication skills in English. Ability to work independently and collaboratively in a fast-paced environment. Proficiency in regulatory Be a part of a young, dynamic, and rapidly growing company. Opportunity to lead and shape the regulatory landscape for semi-regulated markets. Work in a supportive and collaborative team environment. Enjoy a 5-day work week. Competitive salary and growth opportunities. Job Type: Full-time Pay: From ₹18,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Work Location: In person Application Deadline: 29/08/2025
Job Title: Jr. Regulatory Affairs (Semi-Regulated Markets) Company: GenAide Pharmaceutical Pvt Ltd Location: 909, Satyamev Eminence, Science City Road, Near Shukan Mall, Sola, Ahmedabad, Gujarat 380060 About GenAide Pharmaceutical Pvt Ltd: GenAide Pharmaceutical Pvt Ltd is a young, energetic, and rapidly growing pharmaceutical company committed to delivering high-quality healthcare products. We foster a dynamic work environment with a strong emphasis on teamwork and innovation. Join our already developed team and contribute to our exciting journey! Job Type: Full-time Working Days: Monday to Friday (5-day work week) Salary: INR 150000 - INR 300000 per annum Experience: 01-02 years in Regulatory Affairs, with a strong focus on semi-regulated markets. Job Summary: GenAide Pharmaceutical Pvt Ltd is seeking an experienced and highly motivated Regulatory In-charge to lead our regulatory team for semi-regulated markets. The ideal candidate will be responsible for overseeing all regulatory activities, ensuring compliance with local and international regulations, and facilitating timely product registrations in these key regions. This leadership role requires a proactive approach, excellent communication skills, and a deep understanding of regulatory pathways in diverse semi-regulated environments. Key Responsibilities: Regulatory Strategy & Planning: Develop and implement effective regulatory strategies for product registration, lifecycle management, and post-market surveillance in semi-regulated markets. Dossier Preparation & Submission: Oversee the preparation, compilation, and submission of high-quality regulatory dossiers (e.g., CTD, ACTD, country-specific formats) to health authorities in semi-regulated countries. Team Leadership & Mentorship: Lead, mentor, and guide a team of regulatory professionals, fostering a collaborative and high-performance environment. Provide technical expertise and support to the team. Compliance & Due Diligence: Ensure all regulatory activities comply with applicable national and international guidelines, Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs). Conduct regulatory intelligence and assess the impact of new regulations. Health Authority Liaison: Act as the primary point of contact with regulatory agencies in semi-regulated markets, managing queries, providing responses, and facilitating approvals. Artwork & Labeling Review: Review and approve product artworks, labeling, and promotional materials for compliance with regulatory requirements. Post-Approval Variations: Manage and submit post-approval variations, renewals, and other lifecycle management activities for registered products. Cross-functional Collaboration: Collaborate effectively with internal departments such as R&D, Quality Assurance, Production, Sales, and Marketing to ensure regulatory requirements are integrated into business processes. Documentation & Record Keeping: Maintain accurate and up-to-date regulatory documentation and databases. Qualifications: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related scientific discipline. 1-2 years of progressive experience in Regulatory Affairs within the pharmaceutical industry, specifically with a strong track record in semi-regulated markets. In-depth knowledge of regulatory guidelines and requirements for various semi-regulated countries (e.g., ASEAN, LATAM, Africa, CIS regions, etc.). Proven experience in leading and managing a regulatory team. Excellent understanding of dossier requirements (e.g., CTD/ACTD structure). Strong analytical, problem-solving, and decision-making skills. Exceptional written and verbal communication skills in English. Ability to work independently and collaboratively in a fast-paced environment. Proficiency in regulatory Be a part of a young, dynamic, and rapidly growing company. Opportunity to lead and shape the regulatory landscape for semi-regulated markets. Work in a supportive and collaborative team environment. Enjoy a 5-day work week. Competitive salary and growth opportunities. Job Type: Full-time Pay: From ₹18,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Work Location: In person Application Deadline: 29/08/2025
Job Title: Jr. Regulatory Affairs (Semi-Regulated Markets) Company: GenAide Pharmaceutical Pvt Ltd Location: 909, Satyamev Eminence, Science City Road, Near Shukan Mall, Sola, Ahmedabad, Gujarat 380060 About GenAide Pharmaceutical Pvt Ltd: GenAide Pharmaceutical Pvt Ltd is a young, energetic, and rapidly growing pharmaceutical company committed to delivering high-quality healthcare products. We foster a dynamic work environment with a strong emphasis on teamwork and innovation. Join our already developed team and contribute to our exciting journey! Job Type: Full-time Working Days: Monday to Friday (5-day work week) Salary: INR 150000 - INR 300000 per annum Experience: 01-02 years in Regulatory Affairs, with a strong focus on semi-regulated markets. Job Summary: GenAide Pharmaceutical Pvt Ltd is seeking an experienced and highly motivated Regulatory In-charge to lead our regulatory team for semi-regulated markets. The ideal candidate will be responsible for overseeing all regulatory activities, ensuring compliance with local and international regulations, and facilitating timely product registrations in these key regions. This leadership role requires a proactive approach, excellent communication skills, and a deep understanding of regulatory pathways in diverse semi-regulated environments. Key Responsibilities: Regulatory Strategy & Planning: Develop and implement effective regulatory strategies for product registration, lifecycle management, and post-market surveillance in semi-regulated markets. Dossier Preparation & Submission: Oversee the preparation, compilation, and submission of high-quality regulatory dossiers (e.g., CTD, ACTD, country-specific formats) to health authorities in semi-regulated countries. Team Leadership & Mentorship: Lead, mentor, and guide a team of regulatory professionals, fostering a collaborative and high-performance environment. Provide technical expertise and support to the team. Compliance & Due Diligence: Ensure all regulatory activities comply with applicable national and international guidelines, Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs). Conduct regulatory intelligence and assess the impact of new regulations. Health Authority Liaison: Act as the primary point of contact with regulatory agencies in semi-regulated markets, managing queries, providing responses, and facilitating approvals. Artwork & Labeling Review: Review and approve product artworks, labeling, and promotional materials for compliance with regulatory requirements. Post-Approval Variations: Manage and submit post-approval variations, renewals, and other lifecycle management activities for registered products. Cross-functional Collaboration: Collaborate effectively with internal departments such as R&D, Quality Assurance, Production, Sales, and Marketing to ensure regulatory requirements are integrated into business processes. Documentation & Record Keeping: Maintain accurate and up-to-date regulatory documentation and databases. Qualifications: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related scientific discipline. 1-2 years of progressive experience in Regulatory Affairs within the pharmaceutical industry, specifically with a strong track record in semi-regulated markets. In-depth knowledge of regulatory guidelines and requirements for various semi-regulated countries (e.g., ASEAN, LATAM, Africa, CIS regions, etc.). Proven experience in leading and managing a regulatory team. Excellent understanding of dossier requirements (e.g., CTD/ACTD structure). Strong analytical, problem-solving, and decision-making skills. Exceptional written and verbal communication skills in English. Ability to work independently and collaboratively in a fast-paced environment. Proficiency in regulatory Be a part of a young, dynamic, and rapidly growing company. Opportunity to lead and shape the regulatory landscape for semi-regulated markets. Work in a supportive and collaborative team environment. Enjoy a 5-day work week. Competitive salary and growth opportunities. Job Type: Full-time Pay: From ₹18,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Work Location: In person Application Deadline: 29/08/2025
Location - Science City, Ahmedabad (Applied Only Ahmedabad Based Candidate) Job Title - Operation Executive Roles And Responsibility - - Handle data entry and maintain accurate project records. - Follow up with suppliers to ensure timely deliveries and updates. - Finding new vendors and Suppliers in different different portals. - Knowledge in Purchase related work. - Build and maintain Good relationship with supplier and Manufacturers . - Communicate via calls, emails, and in-person meetings when needed. - Support project timelines, milestones, and coordination between teams. - Coordinate with internal teams to ensure alignment between project requirements and supplier outputs. Skills Required - - Qualification - MBA and Graduate in Supply Chain - Experience required 01 to 02 years in Purchase Executive. - Strong verbal and written communication skills. - Basic Computer Knowledge. - Excellent follow-up and coordination abilities. - Proficiency in MS Office (Excel, Word, Outlook). - Willingness to occasionally travel to meet suppliers. Preferred Skills: Basic knowledge of project management practices. Experience in vendor management or procurement coordination. Strong relationship-building skills and negotiation abilities. Benefits : Paid leaves Sick leaves 5 days working Other benefits Job Type: Full-time Pay: Up to ₹30,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Work Location: In person
Location - Science City, Ahmedabad (Applied Only Ahmedabad Based Candidate) Job Title - Operation Executive Roles And Responsibility - - Handle data entry and maintain accurate project records. - Follow up with suppliers to ensure timely deliveries and updates. - Finding new vendors and Suppliers in different different portals. - Knowledge in Purchase related work. - Build and maintain Good relationship with supplier and Manufacturers . - Communicate via calls, emails, and in-person meetings when needed. - Support project timelines, milestones, and coordination between teams. - Coordinate with internal teams to ensure alignment between project requirements and supplier outputs. Skills Required - - Qualification - MBA and Graduate in Supply Chain - Experience required 01 to 02 years in Purchase Executive. - Strong verbal and written communication skills. - Basic Computer Knowledge. - Excellent follow-up and coordination abilities. - Proficiency in MS Office (Excel, Word, Outlook). - Willingness to occasionally travel to meet suppliers. Preferred Skills: Basic knowledge of project management practices. Experience in vendor management or procurement coordination. Strong relationship-building skills and negotiation abilities. Benefits : Paid leaves Sick leaves 5 days working Other benefits Job Type: Full-time Pay: Up to ₹30,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Work Location: In person
Job Title: Regulatory In-charge (Semi-Regulated Markets) Company: GenAide Pharmaceutical Pvt Ltd Location: 909, Satyamev Eminence, Science City Road, Near Shukan Mall, Sola, Ahmedabad, Gujarat 380060 About GenAide Pharmaceutical Pvt Ltd: GenAide Pharmaceutical Pvt Ltd is a young, energetic, and rapidly growing pharmaceutical company committed to delivering high-quality healthcare products. We foster a dynamic work environment with a strong emphasis on teamwork and innovation. Join our already developed team and contribute to our exciting journey! Job Type: Full-time Working Days: Monday to Friday (5-day work week) Salary: INR 5,00,000 - INR 7,00,000 per annum Experience: 5 - 8 years in Regulatory Affairs, with a strong focus on semi-regulated markets. Job Summary: GenAide Pharmaceutical Pvt Ltd is seeking an experienced and highly motivated Regulatory In-charge to lead our regulatory team for semi-regulated markets. The ideal candidate will be responsible for overseeing all regulatory activities, ensuring compliance with local and international regulations, and facilitating timely product registrations in these key regions. This leadership role requires a proactive approach, excellent communication skills, and a deep understanding of regulatory pathways in diverse semi-regulated environments. Key Responsibilities: Regulatory Strategy & Planning: Develop and implement effective regulatory strategies for product registration, lifecycle management, and post-market surveillance in semi-regulated markets. Dossier Preparation & Submission: Oversee the preparation, compilation, and submission of high-quality regulatory dossiers (e.g., CTD, ACTD, country-specific formats) to health authorities in semi-regulated countries. Team Leadership & Mentorship: Lead, mentor, and guide a team of regulatory professionals, fostering a collaborative and high-performance environment. Provide technical expertise and support to the team. Compliance & Due Diligence: Ensure all regulatory activities comply with applicable national and international guidelines, Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs). Conduct regulatory intelligence and assess the impact of new regulations. Health Authority Liaison: Act as the primary point of contact with regulatory agencies in semi-regulated markets, managing queries, providing responses, and facilitating approvals. Artwork & Labeling Review: Review and approve product artworks, labeling, and promotional materials for compliance with regulatory requirements. Post-Approval Variations: Manage and submit post-approval variations, renewals, and other lifecycle management activities for registered products. Cross-functional Collaboration: Collaborate effectively with internal departments such as R&D, Quality Assurance, Production, Sales, and Marketing to ensure regulatory requirements are integrated into business processes. Documentation & Record Keeping: Maintain accurate and up-to-date regulatory documentation and databases. Qualifications: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related scientific discipline. 5 to 8 years of progressive experience in Regulatory Affairs within the pharmaceutical industry, specifically with a strong track record in semi-regulated markets. In-depth knowledge of regulatory guidelines and requirements for various semi-regulated countries (e.g., ASEAN, LATAM, Africa, CIS regions, etc.). Proven experience in leading and managing a regulatory team. Excellent understanding of dossier requirements (e.g., CTD/ACTD structure). Strong analytical, problem-solving, and decision-making skills. Exceptional written and verbal communication skills in English. Ability to work independently and collaboratively in a fast-paced environment. Proficiency in regulatory databases and software is a plus. Why Join GenAide Pharmaceutical Pvt Ltd? Be a part of a young, dynamic, and rapidly growing company. Opportunity to lead and shape the regulatory landscape for semi-regulated markets. Work in a supportive and collaborative team environment. Enjoy a 5-day work week. Competitive salary and growth opportunities. Job Types: Full-time, Permanent Pay: Up to ₹6,000,000.00 per year Benefits: Health insurance Leave encashment Paid sick time Paid time off Provident Fund Work Location: In person
Job Title: Regulatory In-charge (Semi-Regulated Markets) Company: GenAide Pharmaceutical Pvt Ltd Location: 909, Satyamev Eminence, Science City Road, Near Shukan Mall, Sola, Ahmedabad, Gujarat 380060 About GenAide Pharmaceutical Pvt Ltd: GenAide Pharmaceutical Pvt Ltd is a young, energetic, and rapidly growing pharmaceutical company committed to delivering high-quality healthcare products. We foster a dynamic work environment with a strong emphasis on teamwork and innovation. Join our already developed team and contribute to our exciting journey! Job Type: Full-time Working Days: Monday to Friday (5-day work week) Salary: INR 5,00,000 - INR 7,00,000 per annum Experience: 5 - 8 years in Regulatory Affairs, with a strong focus on semi-regulated markets. Job Summary: GenAide Pharmaceutical Pvt Ltd is seeking an experienced and highly motivated Regulatory In-charge to lead our regulatory team for semi-regulated markets. The ideal candidate will be responsible for overseeing all regulatory activities, ensuring compliance with local and international regulations, and facilitating timely product registrations in these key regions. This leadership role requires a proactive approach, excellent communication skills, and a deep understanding of regulatory pathways in diverse semi-regulated environments. Key Responsibilities: Regulatory Strategy & Planning: Develop and implement effective regulatory strategies for product registration, lifecycle management, and post-market surveillance in semi-regulated markets. Dossier Preparation & Submission: Oversee the preparation, compilation, and submission of high-quality regulatory dossiers (e.g., CTD, ACTD, country-specific formats) to health authorities in semi-regulated countries. Team Leadership & Mentorship: Lead, mentor, and guide a team of regulatory professionals, fostering a collaborative and high-performance environment. Provide technical expertise and support to the team. Compliance & Due Diligence: Ensure all regulatory activities comply with applicable national and international guidelines, Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs). Conduct regulatory intelligence and assess the impact of new regulations. Health Authority Liaison: Act as the primary point of contact with regulatory agencies in semi-regulated markets, managing queries, providing responses, and facilitating approvals. Artwork & Labeling Review: Review and approve product artworks, labeling, and promotional materials for compliance with regulatory requirements. Post-Approval Variations: Manage and submit post-approval variations, renewals, and other lifecycle management activities for registered products. Cross-functional Collaboration: Collaborate effectively with internal departments such as R&D, Quality Assurance, Production, Sales, and Marketing to ensure regulatory requirements are integrated into business processes. Documentation & Record Keeping: Maintain accurate and up-to-date regulatory documentation and databases. Qualifications: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related scientific discipline. 5 to 8 years of progressive experience in Regulatory Affairs within the pharmaceutical industry, specifically with a strong track record in semi-regulated markets. In-depth knowledge of regulatory guidelines and requirements for various semi-regulated countries (e.g., ASEAN, LATAM, Africa, CIS regions, etc.). Proven experience in leading and managing a regulatory team. Excellent understanding of dossier requirements (e.g., CTD/ACTD structure). Strong analytical, problem-solving, and decision-making skills. Exceptional written and verbal communication skills in English. Ability to work independently and collaboratively in a fast-paced environment. Proficiency in regulatory databases and software is a plus. Why Join GenAide Pharmaceutical Pvt Ltd? Be a part of a young, dynamic, and rapidly growing company. Opportunity to lead and shape the regulatory landscape for semi-regulated markets. Work in a supportive and collaborative team environment. Enjoy a 5-day work week. Competitive salary and growth opportunities. Job Types: Full-time, Permanent Pay: Up to ₹6,000,000.00 per year Benefits: Health insurance Leave encashment Paid sick time Paid time off Provident Fund Work Location: In person