Medella Softgel Pvt. Ltd. is seeking a skilled and detail-oriented QMS Executive to join our Quality Assurance department at our Kathua facility. The ideal candidate will be responsible for managing and enhancing the Quality Management System (QMS) in compliance with GMP, WHO, and ICH guidelines to ensure product quality and regulatory readiness. Key Responsibilities: Implement and maintain QMS documentation, including SOPs, change control, deviation, CAPA, and quality risk management Ensure compliance with regulatory standards and internal quality procedures Conduct and support internal and external audits, prepare audit responses, and follow up on CAPA implementation Manage document control and version control systems efficiently Review and maintain training records and support quality improvement initiatives Coordinate with cross-functional teams such as Production, QC, and R&D to ensure quality compliance Report QMS performance to the management and recommend improvements Candidate Requirements: Education: B.Pharm / M.Pharm / M.Sc in Chemistry or Pharmaceutical Sciences Experience: Minimum 3–5 years of relevant experience in pharmaceutical QMS Knowledge of cGMP, WHO-GMP, ICH, and ISO 9001 standards Strong analytical skills with attention to detail Good communication and interpersonal skills Proficient in MS Office and QMS-related documentation systems Why Join Us? Be part of a WHO-GMP certified and rapidly growing pharmaceutical manufacturing company Work in a regulatory-compliant and professional environment Opportunities for career growth, skill enhancement, and learning Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Medella Softgel Pvt. Ltd. is seeking a dedicated and detail-oriented GLP Executive for the Quality Control department to ensure strict compliance with Good Laboratory Practices (GLP) and industry standards. The ideal candidate will play a critical role in maintaining laboratory integrity, data accuracy, and regulatory compliance in all QC activities . Key Responsibilities: Ensure GLP compliance in all laboratory practices, documentation, and operations. Maintain and monitor lab protocols, SOPs, and equipment calibration records. Conduct routine testing, sampling, and documentation of raw materials, in-process, and finished pharmaceutical products. Perform and review analytical reports, ensuring accuracy, traceability, and integrity. Participate in internal audits, regulatory inspections, and CAPA implementations. Train QC personnel on GLP and laboratory best practices. Maintain proper documentation in line with WHO-GMP, ICH, and regulatory guidelines. Coordinate with QA and R&D teams for cross-functional documentation and compliance activities. Key Requirements: B.Pharm / M.Pharm / M.Sc in Chemistry, Pharmaceutical Sciences, or a related field. Minimum 3–5 years of experience in a GLP-compliant pharmaceutical QC environment. Strong understanding of analytical techniques like HPLC, UV, Dissolution, and Titration. Familiarity with regulatory guidelines (GLP, GMP, ICH, FDA, etc.). Excellent documentation and communication skills. Proficiency in MS Office and laboratory software systems. Why Join Us? Opportunity to work with a leading WHO-GMP certified pharmaceutical manufacturing company. Growth-oriented and compliance-driven work culture. Exposure to state-of-the-art laboratories and best-in-class industry practices. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Medella Softgel Pvt. Ltd. is seeking a skilled and detail-oriented QMS Executive to join our Quality Assurance department at our Kathua facility. The ideal candidate will be responsible for managing and enhancing the Quality Management System (QMS) in compliance with GMP, WHO, and ICH guidelines to ensure product quality and regulatory readiness. Key Responsibilities: Implement and maintain QMS documentation, including SOPs, change control, deviation, CAPA, and quality risk management Ensure compliance with regulatory standards and internal quality procedures Conduct and support internal and external audits, prepare audit responses, and follow up on CAPA implementation Manage document control and version control systems efficiently Review and maintain training records and support quality improvement initiatives Coordinate with cross-functional teams such as Production, QC, and R&D to ensure quality compliance Report QMS performance to the management and recommend improvements Candidate Requirements: Education: B.Pharm / M.Pharm / M.Sc in Chemistry or Pharmaceutical Sciences Experience: Minimum 3–5 years of relevant experience in pharmaceutical QMS Knowledge of cGMP, WHO-GMP, ICH, and ISO 9001 standards Strong analytical skills with attention to detail Good communication and interpersonal skills Proficient in MS Office and QMS-related documentation systems Why Join Us? Be part of a WHO-GMP certified and rapidly growing pharmaceutical manufacturing company Work in a regulatory-compliant and professional environment Opportunities for career growth, skill enhancement, and learning Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Medella Softgel Pvt. Ltd. is seeking a dedicated and detail-oriented GLP Executive for the Quality Control department to ensure strict compliance with Good Laboratory Practices (GLP) and industry standards. The ideal candidate will play a critical role in maintaining laboratory integrity, data accuracy, and regulatory compliance in all QC activities . Key Responsibilities: Ensure GLP compliance in all laboratory practices, documentation, and operations. Maintain and monitor lab protocols, SOPs, and equipment calibration records. Conduct routine testing, sampling, and documentation of raw materials, in-process, and finished pharmaceutical products. Perform and review analytical reports, ensuring accuracy, traceability, and integrity. Participate in internal audits, regulatory inspections, and CAPA implementations. Train QC personnel on GLP and laboratory best practices. Maintain proper documentation in line with WHO-GMP, ICH, and regulatory guidelines. Coordinate with QA and R&D teams for cross-functional documentation and compliance activities. Key Requirements: B.Pharm / M.Pharm / M.Sc in Chemistry, Pharmaceutical Sciences, or a related field. Minimum 3–5 years of experience in a GLP-compliant pharmaceutical QC environment. Strong understanding of analytical techniques like HPLC, UV, Dissolution, and Titration. Familiarity with regulatory guidelines (GLP, GMP, ICH, FDA, etc.). Excellent documentation and communication skills. Proficiency in MS Office and laboratory software systems. Why Join Us? Opportunity to work with a leading WHO-GMP certified pharmaceutical manufacturing company. Growth-oriented and compliance-driven work culture. Exposure to state-of-the-art laboratories and best-in-class industry practices. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Medella Softgel Pvt. Ltd., a leading pharmaceutical manufacturing company, is looking for a highly organized and detail-oriented PPIC Executive to join our team. The candidate will be responsible for coordinating production planning and managing inventory to ensure smooth and efficient manufacturing processes. Key Responsibilities: Develop and implement effective production plans based on sales forecasts and inventory levels Monitor and maintain optimal inventory levels of raw materials, packaging, and finished goods Coordinate with production, quality, and procurement teams for seamless operations Track daily production schedules and adjust as required to meet deadlines Maintain accurate records for inventory and generate regular status reports Manage materials requirement planning (MRP) and support procurement activities Identify and resolve any planning or inventory-related issues proactively Candidate Requirements: MBA in Operations, Supply Chain Management, or related field 1–3 years of experience in PPIC or production planning roles , preferably in the pharmaceutical or manufacturing sector Strong analytical, organizational, and communication skills Proficient in MS Excel and ERP software systems Ability to work collaboratively across departments Why Join Medella Softgel? Be part of a fast-growing and quality-driven pharmaceutical company Gain valuable experience in a regulated manufacturing environment Opportunities for professional development and career growth Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Medella Softgel Pvt. Ltd., a leading pharmaceutical manufacturer, is looking for a skilled and experienced Compression Operator to join our Production Department . The ideal candidate will be responsible for operating and maintaining tablet compression machines, ensuring smooth and compliant production processes. Key Responsibilities: Operate and monitor tablet compression machines as per batch production records (BPR) Perform machine setup, changeover, and cleaning according to SOPs and GMP guidelines Ensure proper documentation and maintenance of equipment logs Monitor in-process parameters and ensure product quality during compression Identify and report equipment malfunctions or deviations to the production supervisor Maintain hygiene and cleanliness in the production area Coordinate with QA, maintenance, and other departments for smooth operations Follow safety and compliance standards as per regulatory norms Candidate Requirements: Minimum qualification: 10+2 or ITI 3–5 years of hands-on experience as a Compression Operator in a pharmaceutical manufacturing unit Familiarity with GMP practices and documentation Ability to work in shifts and handle production equipment independently Strong attention to detail and a responsible work ethic Why Join Medella Softgel? Be part of a reputed and GMP-certified pharmaceutical company Opportunity to work with modern production technologies Supportive work environment with career growth potential Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Medella Softgel Pvt. Ltd., a leading pharmaceutical manufacturer, is looking for a skilled and experienced Compression Operator to join our Production Department . The ideal candidate will be responsible for operating and maintaining tablet compression machines, ensuring smooth and compliant production processes. Key Responsibilities: Operate and monitor tablet compression machines as per batch production records (BPR) Perform machine setup, changeover, and cleaning according to SOPs and GMP guidelines Ensure proper documentation and maintenance of equipment logs Monitor in-process parameters and ensure product quality during compression Identify and report equipment malfunctions or deviations to the production supervisor Maintain hygiene and cleanliness in the production area Coordinate with QA, maintenance, and other departments for smooth operations Follow safety and compliance standards as per regulatory norms Candidate Requirements: Minimum qualification: 10+2 or ITI 3–5 years of hands-on experience as a Compression Operator in a pharmaceutical manufacturing unit Familiarity with GMP practices and documentation Ability to work in shifts and handle production equipment independently Strong attention to detail and a responsible work ethic Why Join Medella Softgel? Be part of a reputed and GMP-certified pharmaceutical company Opportunity to work with modern production technologies Supportive work environment with career growth potential Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Medella Softgel Pvt. Ltd., a leading pharmaceutical manufacturing company, is looking for a highly organized and detail-oriented PPIC Executive to join our team. The candidate will be responsible for coordinating production planning and managing inventory to ensure smooth and efficient manufacturing processes. Key Responsibilities: Develop and implement effective production plans based on sales forecasts and inventory levels Monitor and maintain optimal inventory levels of raw materials, packaging, and finished goods Coordinate with production, quality, and procurement teams for seamless operations Track daily production schedules and adjust as required to meet deadlines Maintain accurate records for inventory and generate regular status reports Manage materials requirement planning (MRP) and support procurement activities Identify and resolve any planning or inventory-related issues proactively Candidate Requirements: MBA in Operations, Supply Chain Management, or related field 1–3 years of experience in PPIC or production planning roles , preferably in the pharmaceutical or manufacturing sector Strong analytical, organizational, and communication skills Proficient in MS Excel and ERP software systems Ability to work collaboratively across departments Why Join Medella Softgel? Be part of a fast-growing and quality-driven pharmaceutical company Gain valuable experience in a regulated manufacturing environment Opportunities for professional development and career growth Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Supplemental Pay: Performance bonus Yearly bonus Work Location: In person