Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibilities: Perform analytical testing of raw materials, in-process samples, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, Dissolution, Titrations, and Wet Chemistry. Preferred who has experience of handling GC and sound knowledge of method development with troubleshooting. Conduct stability studies and prepare related reports. Calibrate and maintain analytical instruments as per SOPs. Document results accurately in laboratory records as per GDP (Good Documentation Practices) . Assist in method validation, method transfer, and verification activities . Ensure compliance with cGMP, GLP, and safety practices in the laboratory. Investigate OOS (Out of Specification), OOT (Out of Trend), and deviations in coordination with QA. Maintain laboratory reagents, standards, and reference substances. Participate in internal audits and support regulatory inspections. Key Skills & Competencies: Hands on experience with HPLC, GC Good knowledge of analytical instruments (HPLC, GC, UV, IR, Dissolution apparatus, etc.). Understanding of ICH guidelines, cGMP, and regulatory requirements . Strong attention to detail and accuracy. Good communication and documentation skills. Ability to work in a team-oriented environment . Job type - Full-time, Permanent Salary - Best in the industry as per candidates capabilities Email ID - [email protected] Job Type: Full-time Benefits: Provident Fund Application Question(s): What is your current CTC? What is your expected CTC? Education: Master's (Preferred) Experience: Quality control: 2 years (Preferred) Location: Bavla, Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person
Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibilities: Perform analytical testing of raw materials, in-process samples, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, Dissolution, Titrations, and Wet Chemistry. Preferred who has experience of handling GC and sound knowledge of method development with troubleshooting. Conduct stability studies and prepare related reports. Calibrate and maintain analytical instruments as per SOPs. Document results accurately in laboratory records as per GDP (Good Documentation Practices) . Assist in method validation, method transfer, and verification activities . Ensure compliance with cGMP, GLP, and safety practices in the laboratory. Investigate OOS (Out of Specification), OOT (Out of Trend), and deviations in coordination with QA. Maintain laboratory reagents, standards, and reference substances. Participate in internal audits and support regulatory inspections. Key Skills & Competencies: Hands on experience with HPLC, GC Good knowledge of analytical instruments (HPLC, GC, UV, IR, Dissolution apparatus, etc.). Understanding of ICH guidelines, cGMP, and regulatory requirements . Strong attention to detail and accuracy. Good communication and documentation skills. Ability to work in a team-oriented environment . Job type - Full-time, Permanent Salary - Best in the industry as per candidates capabilities Email ID - hr@skanttr.com Job Type: Full-time Benefits: Provident Fund Application Question(s): What is your current CTC? What is your expected CTC? Education: Master's (Preferred) Experience: Quality control: 2 years (Preferred) Location: Bavla, Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person
Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibility Documentation & Compliance Preparation, review, and control of SOPs, protocols, and quality documents. Review and issuance of BMR (Batch Manufacturing Record) / BPR (Batch Packaging Record). Ensure compliance with cGMP, GLP, and regulatory requirements (USFDA, EU, WHO, MHRA, etc.) Audits & Inspections Participate in internal audits, vendor audits, and regulatory inspections. Support in CAPA (Corrective and Preventive Actions) implementation. Change Control & Deviation Handling Documentation and investigation of deviations, incidents, OOS, and OOT results. Execution of change control, risk assessment, and quality system improvements. Validation & Qualification Support in process validation, cleaning validation, method validation, and equipment qualification. Review of validation protocols and reports. Training & Awareness Conduct training on quality systems, SOPs, and regulatory updates. Promote quality culture within the organization. Other QA Activities Line clearance and in-process checks in production and packaging. Review and approval of analytical documents (COAs, specifications, test reports). Support in QMS (Quality Management System) activities. Key Skills Required: Sound knowledge of cGMP, ICH, WHO, and regulatory guidelines. Strong documentation and record-keeping skills. Hands on experience in IPQA Activities Good analytical and problem-solving ability. Excellent communication and teamwork skills. Proficiency in MS Office, QMS tools, and documentation software. Job type - Full-time, Permanent Salary - Best in the industry as per candidates capabilities Email ID - hr@skanttr.com Job Type: Full-time Benefits: Provident Fund Education: Master's (Preferred) Experience: Quality assurance: 2 years (Preferred) Location: Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person
Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibilities: Perform analytical testing of raw materials, in-process samples, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, Dissolution, Titrations, and Wet Chemistry. Preferred who has experience of handling GC and sound knowledge of method development with troubleshooting. Conduct stability studies and prepare related reports. Calibrate and maintain analytical instruments as per SOPs. Document results accurately in laboratory records as per GDP (Good Documentation Practices) . Assist in method validation, method transfer, and verification activities . Ensure compliance with cGMP, GLP, and safety practices in the laboratory. Investigate OOS (Out of Specification), OOT (Out of Trend), and deviations in coordination with QA. Maintain laboratory reagents, standards, and reference substances. Participate in internal audits and support regulatory inspections. Key Skills & Competencies: Hands on experience with HPLC, GC Good knowledge of analytical instruments (HPLC, GC, UV, IR, Dissolution apparatus, etc.). Understanding of ICH guidelines, cGMP, and regulatory requirements . Strong attention to detail and accuracy. Good communication and documentation skills. Ability to work in a team-oriented environment . Job type - Full-time, Permanent Salary - Best in the industry as per candidates capabilities Email ID - hr@skanttr.com Job Type: Full-time Benefits: Provident Fund Application Question(s): What is your current CTC? What is your expected CTC? Education: Master's (Preferred) Experience: Quality control: 2 years (Preferred) Location: Bavla, Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person
Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibility Documentation & Compliance Preparation, review, and control of SOPs, protocols, and quality documents. Review and issuance of BMR (Batch Manufacturing Record) / BPR (Batch Packaging Record). Ensure compliance with cGMP, GLP, and regulatory requirements (USFDA, EU, WHO, MHRA, etc.) Audits & Inspections Participate in internal audits, vendor audits, and regulatory inspections. Support in CAPA (Corrective and Preventive Actions) implementation. Change Control & Deviation Handling Documentation and investigation of deviations, incidents, OOS, and OOT results. Execution of change control, risk assessment, and quality system improvements. Validation & Qualification Support in process validation, cleaning validation, method validation, and equipment qualification. Review of validation protocols and reports. Training & Awareness Conduct training on quality systems, SOPs, and regulatory updates. Promote quality culture within the organization. Other QA Activities Line clearance and in-process checks in production and packaging. Review and approval of analytical documents (COAs, specifications, test reports). Support in QMS (Quality Management System) activities. Key Skills Required: Sound knowledge of cGMP, ICH, WHO, and regulatory guidelines. Strong documentation and record-keeping skills. Hands on experience in IPQA Activities Good analytical and problem-solving ability. Excellent communication and teamwork skills. Proficiency in MS Office, QMS tools, and documentation software. Job type - Full-time, Permanent Salary - Best in the industry as per candidates capabilities Email ID - hr@skanttr.com Job Type: Full-time Benefits: Provident Fund Education: Master's (Preferred) Experience: Quality assurance: 2 years (Preferred) Location: Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person