Executive – Instrumentation (Stability) Department: Quality Control Experience: 3 to 5 Years Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Tentative Start Date: 1st January 2026 Job Summary We are looking for experienced and detail-oriented Executives for Instrumentation (Stability) to support Quality Control activities. The role involves stability and in-process testing, handling analytical instruments, maintaining compliance with regulatory requirements, and ensuring data integrity as per cGMP and GLP standards. Key Responsibilities Preparation, review, and implementation of SOPs, Specifications, STPs , and related QC documentation. Handling and documentation of OOS, calibration activities , and GLP-related tasks . Management of QMS documents including Change Control, Deviations, and Laboratory Incidents. Testing and reporting of in-process samples and stability samples as per approved procedures. Operation, calibration, and maintenance of analytical instruments including: HPLC UV–Visible Spectrophotometer FTIR LPC Karl Fischer / Auto Titrator Ensure data integrity compliance , including user access control, audit trail review, and timely documentation. Adherence to and promotion of cGMP, GDP, GLP , and safety practices within the Quality Control laboratory. Support audits, inspections, and internal reviews related to QC and stability studies. Key Skills & Competencies Strong understanding of QC instrumentation and stability studies Working knowledge of regulatory guidelines and documentation practices Attention to detail and strong analytical skills Ability to work independently and as part of a team Good communication and documentation skills Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Paid time off Provident Fund Work Location: In person
Executive – Instrumentation (GLP) Department: Quality Control Experience: 3 to 5 Years Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Job Summary We are seeking a skilled and compliance-focused Executive – Instrumentation (GLP) to support Quality Control laboratory activities. The role involves handling analytical instruments, GLP documentation, calibration activities, and ensuring strict adherence to data integrity, cGMP, and safety requirements. Key Responsibilities Preparation, review, and implementation of SOPs, Specifications, STPs , and related QC documentation. Handling and documentation of OOS, calibration activities , and other GLP-related tasks . Management of QMS documents including Change Control, Deviations, and Laboratory Incidents. Handling, internal calibration, and routine maintenance of analytical instruments including: HPLC UV–Visible Spectrophotometer FTIR LPC Karl Fischer / Auto Titrator Flame Photometer pH Meter Analytical Balances Preparation and standardization of volumetric solutions . Preparation of general reagents as per approved procedures. Handling, control, and documentation of: Reference Standards Impurity Standards Primary Standards Working Standards Qualification and management of working standards , including maintenance of complete and accurate records. Ensure data integrity compliance , including user access control, audit trail review, and system security. Follow and maintain cGMP, GDP, GLP , and safety practices within the Quality Control department. Support internal and external audits and inspections related to GLP and QC operations. Key Skills & Competencies Strong knowledge of GLP and QC laboratory practices Hands-on experience with analytical instrumentation Sound understanding of regulatory and documentation requirements High attention to detail and compliance mindset Good communication and record-keeping skills Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Paid time off Provident Fund Work Location: In person
Executive – Instrumentation (GLP) Department: Quality Control Experience: 3 to 5 Years Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Job Summary We are seeking a skilled and compliance-focused Executive – Instrumentation (GLP) to support Quality Control laboratory activities. The role involves handling analytical instruments, GLP documentation, calibration activities, and ensuring strict adherence to data integrity, cGMP, and safety requirements. Key Responsibilities Preparation, review, and implementation of SOPs, Specifications, STPs , and related QC documentation. Handling and documentation of OOS, calibration activities , and other GLP-related tasks . Management of QMS documents including Change Control, Deviations, and Laboratory Incidents. Handling, internal calibration, and routine maintenance of analytical instruments including: HPLC UV–Visible Spectrophotometer FTIR LPC Karl Fischer / Auto Titrator Flame Photometer pH Meter Analytical Balances Preparation and standardization of volumetric solutions . Preparation of general reagents as per approved procedures. Handling, control, and documentation of: Reference Standards Impurity Standards Primary Standards Working Standards Qualification and management of working standards , including maintenance of complete and accurate records. Ensure data integrity compliance , including user access control, audit trail review, and system security. Follow and maintain cGMP, GDP, GLP , and safety practices within the Quality Control department. Support internal and external audits and inspections related to GLP and QC operations. Key Skills & Competencies Strong knowledge of GLP and QC laboratory practices Hands-on experience with analytical instrumentation Sound understanding of regulatory and documentation requirements High attention to detail and compliance mindset Good communication and record-keeping skills Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Paid time off Provident Fund Work Location: In person
Department: Production Reporting To: Manager – Production Industry: Pharmaceutical / Sterile Manufacturing Experience: 5–10 Years Qualification: ITI / Diploma / B.Pharm / B.Sc. (Technical) Job Summary Responsible for optimizing BFS production processes through effective supervision, preventive and breakdown maintenance, and robust documentation practices. The role ensures smooth production operations, high equipment availability, compliance with cGMP requirements, and readiness for regulatory audits. Key Responsibilities: 1. Production Process Optimization Improve production efficiency through routine inspections, preventive maintenance, and calibration to minimize downtime. Supervise daily BFS production activities to ensure operational efficiency and output quality. Collaborate with cross-functional teams (QA, QC, Engineering, Validation) to optimize manufacturing processes and resolve technical issues. Coordinate production engineering activities to ensure consistent and high-quality output . 2. Equipment Maintenance & Troubleshooting Perform preventive and breakdown maintenance of BFS (Blow-Fill-Seal) machines . Execute routine maintenance activities such as lubrication, inspection, alignment, and minor repairs . Troubleshoot and diagnose complex mechanical, electrical, and process-related issues to ensure uninterrupted production. Conduct regular equipment inspections and recommend maintenance improvements or upgrades . Maintain detailed maintenance records , including repairs, spare parts usage, and machine history. Perform mould changeovers for different pack sizes (500 ml, 250 ml, and 100 ml). 3. Documentation Management Prepare, review, and update Standard Operating Procedures (SOPs) related to production and maintenance. Prepare Master Preventive Maintenance Plans for production equipment. Maintain and review equipment operation and preventive maintenance logbooks . Review filling-related sections of Batch Manufacturing Records (BMRs) for accuracy and compliance. Ensure proper archiving, traceability, and retrieval of documents for audits and inspections. Prepare and support documentation for regulatory audits and inspections . Review documentation for accuracy, completeness, and GMP compliance . Coordinate with Quality Assurance (QA) for deviations, change controls, and CAPA activities. Ensure batch records are properly reviewed and completed prior to product release. 4. Coordination & Communication Work closely with Production, QA, QC, and Validation teams for smooth operations and documentation flow. Support investigations related to deviations, non-conformances, and customer complaints . Provide training to operators and staff on equipment operation, documentation practices, and GMP compliance. Identify and implement continuous improvement initiatives in production and documentation practices. Stay updated with current regulatory guidelines and industry trends related to sterile manufacturing and documentation. Support internal and external audits by providing required documentation and technical explanations. Machine Exposure / Hands-on Experience STERIMAX BFS 8166 STERIMAX BP 360 BREVETTI ANGELA SYFPAC BFS Machine BFS 7510 HUNAN GLADDEN ISBM Machine Key Skills & Competencies Strong expertise in BFS technology and sterile manufacturing In-depth knowledge of preventive & breakdown maintenance Excellent GMP documentation and audit readiness Problem-solving and root cause analysis skills Effective communication and team coordination Ability to train and mentor technical staff Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Department: Production / Engineering Experience: 2–5 Years Qualification: ITI / Diploma / B.Sc. / B.Pharm Job Summary The role is responsible for operating the Form-Fill-Seal (FFS) machine, ensuring smooth production operations, performing routine preventive maintenance, handling breakdowns, and maintaining accurate production and batch documentation in compliance with cGMP requirements. Key Responsibilities Operate FFS (Form-Fill-Seal) machines as per approved SOPs and production schedules. Perform routine checks before, during, and after machine operation to ensure optimal performance. Carry out preventive maintenance activities as per maintenance plans and schedules. Identify machine abnormalities and perform corrective actions during breakdowns to minimize downtime. Coordinate with Engineering / Maintenance teams for major breakdowns and troubleshooting. Maintain and update daily machine logbooks , equipment usage records, and maintenance logs. Ensure accurate and timely completion of BPCR (Batch Production & Control Records) . Follow and comply with cGMP, GDP, and safety guidelines at all times. Ensure housekeeping and cleanliness of the machine and work area. Support audits, inspections, and internal reviews related to production and equipment. Key Skills & Competencies Hands-on experience with FFS machine operation Knowledge of preventive and corrective maintenance practices Strong understanding of production documentation and BPCR Awareness of cGMP and safety practices Good troubleshooting and problem-solving skills Ability to work in shifts and as part of a team Job Types: Full-time, Permanent, Fresher Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund
Department: Production / Engineering Experience: 2–5 Years Qualification: ITI / Diploma / B.Sc. / B.Pharm (as applicable) Job Summary The role is responsible for the operation of the SWSS (Sterilizer) machine , ensuring effective sterilization processes, performing preventive maintenance, handling machine breakdowns, and maintaining accurate production and batch documentation in compliance with cGMP requirements. Key Responsibilities Operate the SWSS (Sterilizer) machine as per approved SOPs and validated parameters. Monitor sterilization cycles, critical process parameters, and alarms to ensure compliance. Perform routine and preventive maintenance activities as per the maintenance schedule. Identify equipment malfunctions and carry out corrective actions during machine breakdowns to minimize downtime. Coordinate with Engineering / Maintenance teams for complex troubleshooting and repairs. Maintain daily equipment logbooks , sterilization cycle records, and maintenance logs. Ensure accurate and timely documentation of BPCR (Batch Production & Control Records) . Follow and maintain cGMP, GDP, GLP , and safety practices in the production area. Ensure equipment cleanliness, proper housekeeping, and adherence to safety protocols. Support internal and external audits, validations, and regulatory inspections related to sterilization operations. Key Skills & Competencies Hands-on experience in SWSS / sterilizer machine operation Knowledge of sterilization principles and critical parameters Understanding of preventive and corrective maintenance practices Strong documentation and compliance orientation Basic troubleshooting and analytical skills Ability to work in shifts and in a controlled manufacturing environment Job Types: Full-time, Permanent, Fresher Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Department: Quality Assurance Reporting To: Manager – QA / Production Experience: 2–5 Years Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. Shift: Three-shift operation Job Summary Responsible for monitoring manufacturing activities to ensure compliance with cGMP, SOPs, and regulatory requirements . The role involves line clearance, in-process monitoring, batch record verification, and accurate documentation to ensure consistent product quality and regulatory compliance. Key Responsibilities Monitor and supervise manufacturing activities in accordance with cGMP, approved SOPs, and regulatory guidelines . Perform line clearance before start-up, during changeovers, and after batch completion. Verify and review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) for accuracy, completeness, and compliance. Ensure all manufacturing operations are executed strictly as per approved MFR (Master Formula Record) . Perform and document in-process checks (IPC) during various stages of manufacturing. Ensure timely and accurate documentation of manufacturing activities in logbooks, batch records, and related formats. Identify, document, and escalate deviations or non-conformances to QA/Production management. Ensure adherence to data integrity and GDP practices during documentation. Coordinate with Production, QA, and QC teams to maintain smooth manufacturing operations. Work effectively in three-shift operations as per production requirements. Support internal and external audits and inspections related to manufacturing activities. Key Skills & Competencies Strong knowledge of cGMP and regulatory requirements Hands-on experience in line clearance and in-process monitoring Sound understanding of BMR, BPR, and MFR Good documentation and compliance orientation Attention to detail and analytical skills Ability to work in rotational shifts Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹45,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Department: Quality Assurance Reporting To: Manager – QA Experience: 2–5 Years Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. Job Summary Responsible for performing sampling activities and in-process quality checks to ensure compliance with cGMP, SOPs, and regulatory requirements . The role ensures sample integrity, correct sampling practices, and accurate documentation to support product quality and regulatory compliance. Key Responsibilities Perform sampling activities as per approved SOPs and sampling plans. Monitor manufacturing processes during sampling to ensure compliance with cGMP requirements . Collect finished product samples in accordance with approved procedures. Ensure sample integrity is maintained during collection, labeling, storage, and transfer. Verify that sampling tools and accessories are clean, sterile (where applicable), and released for use prior to sampling. Confirm qualification status of sampling areas and equipment before initiating sampling activities. Verify sample labels for accuracy, completeness, and traceability of contents. Perform and document in-process quality checks (IPQC / IPC) as per approved procedures. Record all sampling and IPQC activities accurately in logbooks and relevant formats, following GDP practices . Report deviations, non-conformances, or abnormalities to QA/QC management. Support internal and external audits and inspections related to sampling and in-process quality activities. Key Skills & Competencies Strong knowledge of cGMP and sampling procedures Experience in in-process quality monitoring and IPQC activities Understanding of sample handling, labeling, and integrity requirements Good documentation and compliance mindset Attention to detail and observational skills Ability to work in a regulated manufacturing environment Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹50,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Department: Maintenance & Utility Reporting To: Manager – Maintenance Experience: 3-8 years Qualification: ITI (Electrical) / Diploma / B.Pharm Industry: Pharmaceutical Manufacturing - LVP Job Summary An experienced Maintenance Professional responsible for ensuring uninterrupted operation, preventive maintenance, and compliance of pharmaceutical plant utilities, HVAC systems, and production equipment. The role involves hands-on technical expertise, coordination with cross-functional teams, and adherence to cGMP, safety, and regulatory requirements. Key ResponsibilitiesUtilities & Facility Maintenance Operation, monitoring, and maintenance of HVAC systems to ensure controlled environmental conditions. Handling and maintenance of pharmaceutical water systems , Multicolumn Distillation Plant , and Pure Steam Generator (PSG) . Operation and upkeep of Boilers, DG Sets, Air Compressors, Chillers , and ETP systems . Ensuring uninterrupted utility supply to production and quality areas. Production Equipment Maintenance Preventive and breakdown maintenance of production and packaging equipment including: Linear Vial Washing Machines Autoclaves Filling & Sealing Machines (BFS Systems) Visual Inspection Machines Gumming and Sticker Labeling Machines Troubleshooting electrical and mechanical issues to minimize downtime. Maintenance Planning & Compliance Execution of preventive maintenance schedules and timely corrective actions during breakdowns. Preparation and maintenance of equipment logbooks, maintenance records, and utility documentation as per GMP requirements. Support validation, qualification, and requalification activities for utilities and equipment. Ensure compliance with cGMP, GDP, safety standards , and internal SOPs. Coordination & Supervision Effective utilization of manpower and resources to achieve maximum operational efficiency. Coordination with Production, QA, and external vendors for maintenance and service activities. Regular reporting to Manager – Maintenance on equipment status, breakdowns, and improvement actions. Key Skills & Competencies Strong hands-on knowledge of pharma utilities and HVAC systems Expertise in electrical maintenance and troubleshooting Knowledge of preventive and corrective maintenance practices Understanding of GMP documentation and compliance Team leadership, coordination, and communication skills Ability to work independently and under pressure Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹60,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Department: Engineering / Utilities Experience: 2–5 Years (adjustable as needed) Qualification: ITI / Diploma / B.Sc. / B.Pharm (as applicable) Job Summary The role is responsible for the operation, monitoring, and maintenance of the pharmaceutical water system , ensuring uninterrupted supply of compliant water. The position includes preventive maintenance, breakdown handling, system sanitization activities, and accurate documentation in line with cGMP requirements. Key Responsibilities Operate and monitor water systems (e.g., RO, DM, EDI, WFI, PW) as per approved SOPs and validated parameters. Ensure continuous availability of water meeting pharmacopoeia and quality standards . Perform preventive maintenance activities as per approved maintenance schedules. Identify system abnormalities and take corrective actions during breakdowns to minimize downtime. Carry out and support passivation, sanitization, and PSG (Pure Steam Generator) related activities , as applicable. Maintain daily system logbooks , operating records, maintenance logs, and sanitization records. Ensure timely and accurate documentation of BPCR (Batch Production & Control Records) wherever applicable. Follow and maintain cGMP, GDP, GLP , and safety practices within the utility area. Support validation, qualification, and requalification activities for water systems. Coordinate with QA, Production, and Maintenance teams during audits and inspections. Key Skills & Competencies Hands-on experience with pharma water systems Knowledge of preventive and corrective maintenance practices Understanding of passivation, sanitization, and PSG operations Strong documentation and compliance orientation Basic troubleshooting and analytical skills Ability to work in shifts and controlled utility environments Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person