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
Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibility Plan& execute marketing activities Conduct Market and competitor research Prepare reports, presentation & maintain data Support sales/marketing team in campaigns Key Skills Required: Graduate in any field Proficiency in MS Office & Advance Excel Strong communication and interpersonal skills Fresher to 1 yr experience Immediate Joining Office work (no field work or work from home) Job type - Full-time, Permanent Salary - 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 ? How soon you can join the organization? Education: Bachelor's (Preferred) Experience: Marketing : 1 year (Preferred) Location: Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person
Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibility Plan& execute marketing activities Conduct Market and competitor research Prepare reports, presentation & maintain data Support sales/marketing team in campaigns Key Skills Required: Graduate in any field Proficiency in MS Office & Advance Excel Strong communication and interpersonal skills Fresher to 1 yr experience Immediate Joining Office work (no field work or work from home) Job type - Full-time, Permanent Salary - 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 ? How soon you can join the organization? Education: Bachelor's (Preferred) Experience: Marketing : 1 year (Preferred) Location: Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person
Skanttr Lifescience LLP (API Manufacturing) Location - Bavla , Ahmedabad Key Responsibility Plan& execute marketing activities Conduct Market and competitor research Prepare reports, presentation & maintain data Support sales/marketing team in campaigns Key Skills Required: Graduate in any field Proficiency in MS Office & Advance Excel Strong communication and interpersonal skills Fresher to 1 yr experience Immediate Joining Office work (no field work or work from home) Job type - Full-time, Permanent Salary - 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 ? How soon you can join the organization? Education: Bachelor's (Preferred) Experience: Marketing : 1 year (Preferred) Location: Ahmedabad, Gujarat (Required) Willingness to travel: 25% (Preferred) Work Location: In person
Company Description Skanttr Lifescience LLP is a pharmaceutical manufacturing company based in Gujarat, India. We specialize in producing various compounds such as PPI, Anti-Diabetics, Cholesterol-lowering drugs, Antihypertensive, Antidepressants, Antiviral, and Anti-Psychotic. Additionally, custom API contract manufacturing is one of our core proficiencies. Role Description This is a full-time on-site role for a Senior Quality Assurance Executive, located in Bavla. The Senior Quality Assurance Executive will be responsible for overseeing and ensuring product quality, conducting quality audits, managing quality control processes, and implementing quality management systems. Day-to-day tasks include reviewing production processes, conducting inspections, and ensuring compliance with industry standards and regulations. Qualifications Prepare , review and controls SOPs, protocol, Documentation. Ensure compliance with eGMP, GLP, and regulatory requirements. Change control and deviation handling. Participate in audits and support in CAPA implementation. Review and approval of Analytical documents (COAs , specifications, test reports) Strong attention to detail and analytical skills Excellent written and verbal communication skills Ability to work independently and manage multiple tasks B.Sc / M.Sc Chemistry , Microbiology, Biotechnology, B.Pharm , M.Pharm Experience in the API pharmaceutical industry is a plus
Key Qualifications M.Sc. in Organic Chemistry 2–5 years Salary best in the market (as per candidate capabilities ) Key Responsibilities Design, plan, and execute multi-step organic syntheses for APIs, intermediates, and novel compounds. Conduct literature survey, reaction design, and optimization of synthetic routes. Perform purification techniques (column chromatography, recrystallization, distillation, etc.). Characterize compounds using modern analytical techniques (NMR, IR, HPLC, GC, LC-MS, etc.). Maintain accurate experimental records and prepare reports, lab notebooks, and SOPs. Ensure compliance with laboratory safety protocols and GLP/GMP standards. Collaborate with cross-functional teams in scale-up, process development, and technology transfer. Contribute to problem-solving and troubleshooting of synthetic challenges. Required Skills & Competencies Strong theoretical and practical knowledge of organic synthesis and reaction mechanisms. Hands-on experience with synthetic methodologies, purification, and analytical characterization. Ability to design synthetic routes and optimize reaction conditions. Good understanding of ICH, cGMP, and regulatory requirements (preferred). Excellent problem-solving, analytical, and documentation skills. Strong teamwork, communication, and time-management abilities. Job Types: Full-time, Permanent Benefits: Provident Fund Ability to commute/relocate: Bavla, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): What is your current CTC? What is your expected CTC? Notice period ? Are you comfortable with API Manufacturing? Are you comfortable with bavla location? Work Location: In person
Key Qualifications M.Sc. in Organic Chemistry 2–5 years Salary best in the market (as per candidate capabilities ) Key Responsibilities Design, plan, and execute multi-step organic syntheses for APIs, intermediates, and novel compounds. Conduct literature survey, reaction design, and optimization of synthetic routes. Perform purification techniques (column chromatography, recrystallization, distillation, etc.). Characterize compounds using modern analytical techniques (NMR, IR, HPLC, GC, LC-MS, etc.). Maintain accurate experimental records and prepare reports, lab notebooks, and SOPs. Ensure compliance with laboratory safety protocols and GLP/GMP standards. Collaborate with cross-functional teams in scale-up, process development, and technology transfer. Contribute to problem-solving and troubleshooting of synthetic challenges. Required Skills & Competencies Strong theoretical and practical knowledge of organic synthesis and reaction mechanisms. Hands-on experience with synthetic methodologies, purification, and analytical characterization. Ability to design synthetic routes and optimize reaction conditions. Good understanding of ICH, cGMP, and regulatory requirements (preferred). Excellent problem-solving, analytical, and documentation skills. Strong teamwork, communication, and time-management abilities. Job Types: Full-time, Permanent Benefits: Provident Fund Ability to commute/relocate: Bavla, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): What is your current CTC? What is your expected CTC? Notice period ? Are you comfortable with API Manufacturing? Are you comfortable with bavla location? Work Location: In person
As a Research and Development Executive at Skanttr, a pharmaceutical manufacturing company in Gujarat, India, your role will involve overseeing and conducting R&D activities to formulate new products and optimize existing ones. You will be responsible for documenting and analyzing research findings to ensure product innovation aligns with industry standards and regulations. Key Responsibilities: - Design, plan, and execute multi-step organic synthesis for APIs, intermediates, and novel compounds. - Experience with synthetic methodologies, purification, and analytical characteristics. - Perform purification techniques such as column chromatography, recrystallization, and distillation. - Strong analytical and problem-solving skills. - Excellent written and verbal communication skills. - Ability to work independently and collaboratively in a team setting. - Maintain accurate experimental records and prepare reports. - Characterize compounds using modern analytical techniques such as NMR, IR, HPLC, GC, LC-MS, etc. Qualifications: - Bachelor's or Master's degree in Organic Chemistry. - Good understanding of ICH, cGMP, and regulatory requirements. - 1-5 years of experience in a similar role. Please note that this is a full-time on-site position located in Bavla. Skanttr specializes in producing a variety of compounds, including PPI, anti-diabetics, cholesterol-lowering drugs, antihypertensive, antidepressants, antiviral, and antipsychotic medications. Additionally, custom API contract manufacturing is a core proficiency of the company, allowing for meeting specific client needs with precision.,