PRG PHARMA PVT LTD

Experience: 10 years Job Location: Pitampura Qualification: MBA, M.COM, CA (Kindly Apply Male candidates only) . · Verifying Invoices raised by vendors, scrutinizing all particulars and Coordinating with higher officials to release payment on time. · Preparation of Details of GSTR 1 Statement of Outward Supplies of Goods and Services and E-Filling of GSTR 1 Return. · Preparation of Details of Inward Purchases of Taxable Goods and Services. · Check & Preparation of Reverse Charge Mechanism (RCM) Liability Finalized for Payment on monthly basic. · Preparation of Details of GSTR 3B Summarize the details of Outward & Inward Supplies and E-Filling of GSTR 3B Return. · Preparation of e-way bill from E- way bill Portal. · Finalization of Annual Returns details (GSTR 9 and 9C) of Goods and Services. · TDS Deduction on Contractor, Professional, Rent, Purchase of Goods-194Q & Interest. · Finalization of TDS for Payment on monthly basic and Filling of TDS Returns (Form 26Q). · Handling all functions of Accounts Receivable and Payable including Debtors / Creditors reconciliation and Bank Reconciliation. Job Type: Full-time Pay: ₹40,000.00 - ₹50,000.00 per month Schedule: Day shift Ability to commute/relocate: Pitampura, Delhi - 110034, Delhi: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Accounting: 10 years (Required) Work Location: In person

kindly apply male candidates only .Freshers can apply . Key Responsibilities: Perform data entry, maintain databases, and update records with high accuracy. Prepare and format documents, reports, and presentations using MS Word and Excel. Handle and manage incoming and outgoing communication, including emails and calls, as required. Provide administrative support to assigned departments and assist with operational processes. Assist with generating reports, analyzing data, and presenting findings to management. Maintain an organized filing system, both digital and physical, ensuring easy access to information. Key Skills & Qualifications: Proficiency in MS Excel (advanced functions like VLOOKUP, pivot tables, data analysis) and MS Word. Strong attention to detail with excellent organizational skills. Ability to multitask and manage time effectively. Strong communication skills, both written and verbal. Willingness to learn new skills and adapt to changing requirements. Previous experience in a back-office or administrative role is a plus but not required. Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Schedule: Day shift Work Location: In person

kindly apply male candidates only .Freshers can apply . Key Responsibilities: Perform data entry, maintain databases, and update records with high accuracy. Prepare and format documents, reports, and presentations using MS Word and Excel. Handle and manage incoming and outgoing communication, including emails and calls, as required. Provide administrative support to assigned departments and assist with operational processes. Assist with generating reports, analyzing data, and presenting findings to management. Maintain an organized filing system, both digital and physical, ensuring easy access to information. Key Skills & Qualifications: Proficiency in MS Excel (advanced functions like VLOOKUP, pivot tables, data analysis) and MS Word. Strong attention to detail with excellent organizational skills. Ability to multitask and manage time effectively. Strong communication skills, both written and verbal. Willingness to learn new skills and adapt to changing requirements. Previous experience in a back-office or administrative role is a plus but not required. Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Schedule: Day shift Work Location: In person

You should be a candidate from the Pharma Industry to: Design, implement, and manage quality control systems to ensure products meet established standards and specifications. Develop and maintain quality control procedures and documentation. Establish and enforce quality control and compliance standards across all departments. Manage Functions of Quality Control Systems, CGMP compliance, and Validations. Analyze Raw Materials & Finished Products. Manage the laboratory teams and determine work priorities. Daily plan analysis and ensure the analysis of raw materials, intermediates, and in-process controls. Have control over day-to-day activities of the QC Dept with Chemical Laboratory, Instrumentation & Microbiology. Analyze quality control test results and provide feedback and interpretation to production management or staff. Conduct regular inspections and tests on incoming raw materials, in-process production, and finished products. Monitor and analyze quality performance, identifying trends and areas for improvement. Investigate and resolve customer complaints related to product quality. Be responsible for defining operational strategy and road map for Quality Assurance management at the site. Execute site Quality Assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives, and regulatory requirements. Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at the site. Be responsible for batch disposition of the products. Provide strong leadership and expertise to ensure the achievement of all Quality Assurance goals - business and functional at the site. Identify and implement solutions for improving existing site Quality Assurance systems and processes. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews, and the provision of training and development opportunities. This is a full-time job with a day shift schedule and requires in-person work location.,

Pharma background candidates only We are hiring Regulatory Affairs Executives (freshers) for our Regulatory Department — a great opportunity to start your career in a growing pharmaceutical company. Key Responsibilities: 1. Review and compilation of dossiers 2.Handling regulatory queries 3.Exposure to ROW marketsRegulatory Documentation & Dossier Preparation. 4.Prepare, review, and compile regulatory submissions (CTD/eCTD/ACTD formats) for ROW, semi-regulated, and regulated markets. 5.Manage variations, renewals, and updates for existing product registrations. Regulatory Compliance: Ensure compliance with national and international regulatory requirements. Review and approve artwork and product labeling to meet local regulatory guidelines. Maintain regulatory files and documentation as per applicable regulations. Interested candidates can share their CVs at [email protected] Job Type: Full-time Pay: ₹18,000.00 - ₹21,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Pharma background candidates only We are hiring Regulatory Affairs Executives (freshers) for our Regulatory Department — a great opportunity to start your career in a growing pharmaceutical company. Key Responsibilities: 1. Review and compilation of dossiers 2.Handling regulatory queries 3.Exposure to ROW marketsRegulatory Documentation & Dossier Preparation. 4.Prepare, review, and compile regulatory submissions (CTD/eCTD/ACTD formats) for ROW, semi-regulated, and regulated markets. 5.Manage variations, renewals, and updates for existing product registrations. Regulatory Compliance: Ensure compliance with national and international regulatory requirements. Review and approve artwork and product labeling to meet local regulatory guidelines. Maintain regulatory files and documentation as per applicable regulations. Interested candidates can share their CVs at hrsupport@prgpharma.com Job Type: Full-time Pay: ₹18,000.00 - ₹21,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Job Responsibilities;- Control manufacturing activities in the respective section to ensure activities carried out are as per requirement of cGMP & safety to meet the quality and manufacturing targets in time. I. Monitor and control planned production by daily activity review as per production plan to meet production targets and quality standards II. Ensure maintenance is carried out as per standards to realise optimum utilisation of manufacturing consumables III. Prepare, review and update GMP documents to meet regulatory compliance and quality of product IV. Ensure adequate and trained manpower availability across shifts to ensure production continuity V. Monitor employee and workplace safety to maintain safe environment VI. Implement management initiatives and manufacturing excellence practices for continuous improvement Educational Qualification M.Sc /B.Pharm / M.Pharm intrested candidates can send your cv hrsupport@prgpharma.com Job Type: Full-time Pay: ₹70,000.00 - ₹90,000.00 per year Schedule: Day shift Work Location: In person

Job description PRG Pharma, a leading pharmaceutical contract manufacturer headquartered in India, stands out for its state-of-the-art facility dedicated to producing innovative dosage forms of nutraceutical products. Responsibilities :- Develop and Implement strategic plans to expand the company's pharmaceutical product exports in compliance with global regulations . identify and assess new markets for pharmaceutical products, establish partnerships and develop distribution channels . Manage and oversee all aspects of export operations ,including BRC documentation ,Export invoice ,Packing invoice ,e-sanchit documentation ,followup with forwarders and shipping logistics . Negotiate contracts ,pricing and terms with distributors ,collaborate closely with internal team such as regulatory affairs ,production . conduct market research and analysis to identify trends ,competitive landscape and opportunities for growth . Requirements :- Male Candidate should be from Pharmaceutical industry only . Bachelor degree in pharmacy ,Business Administration ,or related field. 5-7 years of proven experience in export mangement within the pharmaceutical industry . Strong negotiation ,communication and interpersonal skills . Intrested candidates can apply on hrsupport@prgpharma.com Job Type: Full-time Pay: ₹40,000.00 - ₹50,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Kindly Apply Male candidates Key Skills required-: We are seeking an experienced and detail-oriented Quality Control Manager to oversee all aspects of our quality management system. The ideal candidate will be responsible for developing and implementing quality control processes, ensuring compliance with industry standards and regulations, and driving continuous improvement initiatives to enhance product quality and customer satisfaction. ● Design, implement, and manage quality control systems to ensure products meet established standards and specifications ● Develop and maintain quality control procedures and documentation ● Establish and enforce quality control and compliance standards across all departments ● Managing Functions of Quality Control Systems, CGMP compliance, Validations ● Analysis of Raw Materials & Finished Products ● Managing the laboratory teams and determining work priorities ● Daily planning of analysis and ensure analysis of raw materials, intermediates, in-process controls ● Control over day-to-day activities of QC Dept with Chemical Laboratory, Instrumentation & Microbiology ● Analyse quality control test results and provide feedback and interpretation to production management or staff ● Conduct regular inspections and tests on incoming raw materials, in-process production, and finished products ● Monitor and analyze quality performance, identifying trends and areas for improvement ● Investigate and resolve customer complaints related to product quality ● Lead, mentor, and manage a team of quality control inspectors and technicians ● Provide training and guidance to employees on quality control processes and procedures ● Foster a culture of quality and continuous improvement within the team ● Ensure compliance with industry standards, regulations, and certifications ● Stay updated on quality control best practices and industry developments ● Collaborate with regulatory agencies and external auditors to maintain necessary certifications ● Collect and analyze data to evaluate the performance of quality control processes ● Prepare detailed reports and present findings to management, highlighting areas for improvement and successful outcomes ● Identify opportunities for process optimization and cost reduction while maintaining high-quality standards Interested candidates can apply on hrsupport@prgpharma.com Job Type: Full-time Work Location: In person

Apply Male candidates only Key Skills Required :- Responsible for defining operational strategy and road map for Quality Assurance management at site. Execute site Quality Assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. · Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site. · Responsible for batch disposition of the products. · Provide strong leadership and expertise to ensure achievement of all Quality Assurance goals business and functional at site. · Identify and implement solution for improving existing site Quality Assurance systems and processes. · Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. · Ensure that performance issues are managed in a consistent and timely manner. · Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. · Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams. · Responsible for executing Quality Management Reviews at site, monitor individual Performance and set improvement areas. · Responsible for managing the Quality Management Systems ensuring market complaints, failures, deviations are investigated and corrective and preventive actions are implemented as per set timeline. · Responsible for ensuring compliance to regulatory requirements on product, process and release procedures. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. · Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QA systems at the site. · Facilitate internal and regulatory agency audits, ensuring that findings from site audits are understood assessed and addressed site wide in a comprehensive manner. Monitor industry trends/issues faced internally and identify scope for improving site Quality · Assurance management and processes. · The authorization of written procedures and other documents, including amendments. Interested Candidates can apply on hrsupport@prgpharma.com Job Type: Full-time Work Location: In person