Company Description PRG PHARMACEUTICALS PVT. LTD is one of the leading manufacturers and exporters of various (i) Active Pharma Ingredients & Intermediates & (ii) Formulations Manufacturing into the global market. Role Description This is a full-time on-site role for a Chartered Accountant /or practicing (CA) based in Delhi, India. The Chartered Accountant will be responsible for preparing financial statements, managing tax compliance, conducting audits, and providing financial advice. Day-to-day tasks include maintaining financial records, analyzing financial performance, and ensuring regulatory compliance. Qualifications Proficient in preparing financial statements and managing tax compliance Experience in conducting audits and financial analysis Strong knowledge of accounting principles and regulations Excellent analytical and problem-solving skills Attention to detail and high level of accuracy Strong organizational and time-management skills Effective communication and interpersonal skills Ability to work independently and as part of a team Chartered Accountant certification Experience in the pharmaceuticals industry is a plus interested candidates can apply there cv's on hrsupport@prgpharma.com
we are hiring warehouse Manager Location -Narela Delhi Experience -2-3 years qualification - Minimum qualification is D pharma candidates .(B pharm mandatory ) . kindly apply if you have the required skills . Role Description This is a full-time on-site role for a Warehouse Supervisor located in Delhi, India. As a Warehouse Supervisor, you will oversee day-to-day warehouse operations, manage shipping and receiving processes, ensure proper material handling, and maintain inventory control. Duties include supervising staff, managing forklift operations, and ensuring compliance with safety regulations and company policies. Responsibilities: Manage day-to-day warehouse operations. Supervise warehouse staff and ensure productivity. Ensure proper inventory control and accurate records. Coordinate with logistics and supply chain teams. Implement health and safety standards. Optimize warehouse layout and processes for efficiency. Handle reporting and documentation. Interested candidates can share there cv's at hrsupport@prgpharma.com or call @9873110075
Hiring for warehouse Manager Location -Narela Delhi Experience -2-3 years qualification - Minimum qualification is (B pharm) mandatory . NOTE : kindly dont apply if you are not a B pharm candidate . Role Description This is a full-time on-site role for a Warehouse Supervisor located in Delhi, India. As a Warehouse Supervisor, you will oversee day-to-day warehouse operations, manage shipping and receiving processes, ensure proper material handling, and maintain inventory control. Responsibilities: ? Manage day-to-day warehouse operations. ? Supervise warehouse staff and ensure productivity. ? Ensure proper inventory control and accurate records. ? Coordinate with logistics and supply chain teams. Interested candidates can share there cv's at [HIDDEN TEXT] or call @9873110075
📍Open Position: 1) Business Development Manager / Business Development Executives 🌍 Industry: Pharmaceuticals 👩🎓 Experience - 4 to 5 Years 📌 Location – Netaji Subhash Place, Pitampura , Delhi -110034 🎓 Education - BSc or MSc in pharmacy or equivalent, MBA marketing or BD (Preferred). 🌟 Skills Required: “Business Growth” , Client Acquisition , Market Analysis, Sales Targets, Proposal Development, Negotiation, Team Collaboration . *Key Role & Responsibilities:* ✔ Identify and develop new business opportunities to increase revenue and market share. ✔ Build and maintain strong relationships with potential clients, partners, and stakeholders. ✔ Research market trends, competitors, and customer needs to formulate effective strategies. ✔ Set and achieve sales targets to meet company objectives. ✔ Prepare and present compelling proposals to potential clients. *Who Should Apply:* ✅ Minimum of 4 -5 years of proven experience in API sales ,exports or related roles. ✅ A strong understanding of the pharmaceutical industry is a plus. ✅ Excellent communication and presentation skills. ✅ Self-motivated, goal-oriented, and able to work independently. ✅ Proven track record of meeting or exceeding sales targets. ✅ Willingness and ability to generate sufficient business through telephonic discussions. 📧 Send your resume at hrsupport@prgpharma.com or 📞 Contact us @ 9873110075 | + 01145054505
📢 We’re Hiring! Join Our Team at PRG Pharma We have two exciting openings for Business Development Managers (BDM) : BDM – Nutraceuticals & Natural Extracts Minimum 3 years of experience in sales (Nutraceuticals & Natural Extracts) Salary: ₹ upto 6.5 LPA and above 2. BDM – CDMO & Third-Party Manufacturing Minimum 5 years of experience in sales (CDMO & Third-Party Manufacturing) Salary: ₹ upto 9 LPA and above 📩 To Apply: Send your resume to hrsupport@prgpharma.com 📞 Contact: 9873110075
Urgent hiring at PRG Pharma!!! We have two exciting openings for Business Development Managers (BDM): BDM – Nutraceuticals & Natural Extracts Minimum 3 years of experience in sales (Nutraceuticals & Natural Extracts) Salary: ₹ upto 6.5 LPA and above 2. BDM – CDMO & Third-Party Manufacturing Minimum 5 years of experience in sales (CDMO & Third-Party Manufacturing) Salary: ₹ upto 9 LPA and above 📩 To Apply: Send your resume to hrsupport@prgpharma.com 📞 Contact: 9873110075
Title: Assistant Manager Regulatory Affairs Location: Netaji Subhash Place, Pitampura, Delhi Experience Required: 34 Years Department: Regulatory Affairs Employment Type: Full-Time About The Role The Assistant Manager Regulatory Affairs will be responsible for managing regulatory submissions, ensuring compliance with national and international regulatory standards, handling regulatory queries, and supporting product lifecycle management. The ideal candidate should have strong experience with dossier preparation, regulatory documentation, and exposure to ROW, semi-regulated, and regulated markets. Key Responsibilities Regulatory Documentation & Dossier Preparation: Prepare, review, and compile regulatory dossiers in CTD/eCTD/ACTD formats for ROW, semi-regulated, and regulated markets. Ensure timely submission of dossiers for product approvals, renewals, variations, and updates. Maintain high-quality documentation aligned with regulatory requirements and internal standards. Regulatory Submissions Prepare, review, and submit regulatory filings for obtaining and maintaining approvals for medical devices or pharmaceutical products in domestic and international markets. Coordinate with external agencies and regulatory authorities for smooth submission and follow-ups. Regulatory Compliance Ensure adherence to national and global regulatory requirements across all product lines. Review and approve artwork, product labeling, IFU (Instructions for Use), and packaging to ensure compliance with market-specific guidelines. Maintain up-to-date regulatory files, documentation, and related records. Regulatory Queries & Communication Handle regulatory queries from authorities, partners, and internal stakeholders. Provide accurate, well-supported responses in a timely manner to facilitate approvals. Regulatory Strategy Develop and implement regulatory strategies in collaboration with R&D, QA, Manufacturing, and other cross-functional teams. Ensure regulatory considerations are integrated throughout the product lifecyclefrom development to Affairs Support: Collaborate with Clinical Affairs team in planning and executing clinical trials required for regulatory submissions. Assist in preparation of clinical documentation and evidence reports. Post-Market Surveillance Monitor adverse events, customer complaints, and field actions in accordance with regulatory guidelines. Implement CAPA (Corrective and Preventive Action) measures as required. Regulatory Intelligence Stay updated with evolving global regulations, guidelines, and industry trends. Communicate key regulatory changes to relevant departments to ensure business readiness. Audit Preparation & Inspection Readiness Prepare documentation and teams for regulatory audits and inspections. Conduct mock audits and internal assessments to ensure constant readiness. Cross-Functional Collaboration: Work closely with Quality Assurance, R&D, Manufacturing, Marketing, and Supply Chain teams to ensure seamless regulatory alignment. Support internal teams with regulatory insights for product development, labeling, and compliance & Skills: Required Qualifications Bachelors or Masters degree in Pharmacy, Life Sciences, Biotechnology, or related field. 34 years of experience in Regulatory Affairs (pharma/medical devices). Strong understanding of regulatory pathways for ROW and semi-regulated markets. Hands-on experience with CTD/eCTD/ACTD dossier compilation. Technical Skills Knowledge of regulatory frameworks (WHO, USFDA, EMA, CDSCO, etc. Strong understanding of regulatory submission processes and documentation management. Experience reviewing labeling, artwork, and product-related documents. Familiarity with post-market surveillance and CAPA processes. Soft Skills Strong analytical and problem-solving abilities. Effective written and verbal communication skills. Excellent attention to detail and documentation accuracy. Ability to work collaboratively with cross-functional teams. Strong organizational and time-management skills (ref:iimjobs.com)