Role & responsibilities 1. Responsible to review documentation related to Microbiology laboratory. 2. To ensure proper sampling and testing of DI water, raw water and drinking water as per the method of analysis. 3. To ensure environment monitoring program as per the schedule. 4. Responsible for review all the relevant records of microbiology testing. 5. Responsible for review of sanitization of microbiology as per the defined schedule. 6. To ensure qualification and calibration of instrument used for microbiology testing. 7. To ensure the proper temperature, RH and differential pressure monitoring in microbiologist lab. 8. To send sample for microbiology analysis to outside contract labs. 9. To prepare STPs, SOCP, SCPs of QC. 10. Responsible for checking all microbiology log book/records/conduct lab investigation. 11. Responsible for reporting /reviewing of OOS/OOT and to conduct lab investigation. 12. Managing deviation, change control, incidences with investigation and associated CAPA. 13. To review validation/revalidation, qualification studies involved in microbiology. 14. To ensure that STP is followed in analysis. 15. Responsible for preparation of standard operating procedures, validation protocols and execution. 16. To review GMP related protocols and reports. Interested candidates forward resume on anuverma@scllifesciences.com or Whats app/ call on 9988339860.

Key Responsibilities: - Technology Transfer: • Assist in managing the technology transfer process for new products and process for new products and processes from R&D to commercial production. • Collaborate with cross-functional teams including R&D, Manufacturing, Quality and Regulatory Affairs to facilitate successful technology transfer within specified timelines and quality standards. • Contribute to the development and implementation of strategies to mitigate risks associated with technology transfer process. Process Engineering : • Support process engineering activities aimed at optimizing manufacturing processes for efficiency, scalability, and cost effectiveness. • Participate in identifying opportunities for process improvements, conducting studies, and implementing solutions to enhance product quality and yield. • Assist in providing technical guidance to the engineering team to drive continuous improvement initiatives. Compliance and Documentation: • Assist in ensuring compliance with regulatory requirements and industry standards throughout technology transfer and process engineering activities. • Review documentation related to technology transfer, process optimization and validation protocols as needed. Cross Functional Collaboration : • Work collaboratively with other departments to facilitate smooth technology transfer and process improvements. • Support Quality Assurance and Regulatory Affairs in regulatory filings and inspections as required. Leadership and Development: • Support Head of MSTG in providing leadership, mentoring and guiding to the MSTG team, promoting a culture of innovation, teamwork and continuous learning. • Identify training needs and development opportunities for team members to enhance their skills and capabilities. Interested candidates forward resume on anuverma@scllifesciences.com or Whats app/ call on 9988339860.

We are seeking a highly skilled R&D, Group Leader with extensive experience in the Api industry. Individual will lead a team of chemists from R&D. Candidate should have experience in New Product Development , with experience in producing cost-effective, for the synthesis of reliable APIs and intermediates. Education: PhD - Organic Chemistry with around 10-15 years of experience in API Companies. Location: Hyderabad Job Description: 1. To lead a team of chemists from R&D. 2. To develop and produce cost-effective, non-infringing, safe and eco-friendly technologies for the synthesis of reliable APIs and intermediates. 3. Creative capabilities in the areas of organic chemistry in designing and conducting multi step organic synthesis that is very much attractive from commercial aspects. 4. To Identifying and select API molecules based on developing non-infringing process for API molecules. 5. Support in transformations in synthetic organic chemistry aimed at target molecule from R&D scale to plant scale. 6. Conduct research and design experiments to develop and optimize synthetic routes for API molecules. 7. Perform literature searches for identified API molecules to determine synthesis routes, polymorphs, and analytical methods. 8. Conduct experimental trials to assess feasibility and optimize designed synthetic routes for API molecules. 9. Strongly self-motivated, believing in team work and efficient problem solver, having good skills for development of subordinate potentials. 10. Exhibit Good Laboratory Practice. 11. Efficient handling of High pressure, Hazardous, Highly moisture sensitive and other specialized reactions. 12. API- cost effective process development. 13. Impurity impact on process, identification & synthesis. 14. Development of new API molecules and technology transfer of the same. Documentation: *Record all experiments in the laboratory notebook (LNB) and maintain corresponding analytical data in organized folders * Design synthetic routes for the synthesis and isolation of impurities and reference standards. * Ensure all documentation meets Good Manufacturing Practices (GMP) and regulatory standards. Safety and Compliance: • Adhere to all safety protocols and ensure a safe working environment in the laboratory. • Develop non-infringing synthetic processes based on literature, raw material availability, and polymorph studies. • Stay up-to-date with industry trends, regulatory guidelines, and advancements in chemical synthesis and analytical techniques. Interested candidates share resume on anuverma@sauravchemicals.com Contact and what's app on 9988339860

Role & responsibilities Operate and monitor chemical reactions in reactors (GLR, SSR) specifically for bromine handling, ensuring optimal performance and product quality. Oversee the filling process of BPR (Batch Process Reactor) and BCR (Batch Chemical Reactor) with bromine, ensuring accuracy and compliance with safety standards. Perform routine inspections and maintenance of equipment used in bromine processing to prevent downtime and ensure efficient operation. Accurately record and report production data related to bromine handling, including batch quality and process parameters, to maintain operational records. Work closely with team members to troubleshoot and resolve operational issues related to bromine processing, ensuring smooth production flow. Follow all safety protocols and environmental regulations specific to bromine handling during operations to maintain a safe working environment. Location: Saidpura, Derabassi Qualification: 10th, 12th, Diploma Chemical Interested one share their resume on Whatsapp at 9915095113 or email at manik.mehta@scllifesciences.com

Role & responsibilities Preparation and maintenance of training records To prepare specification and method of analysis as per requirement Preparation of protocols and reports Change Control, Analyst Qualification To support lab activities including analysis for method development and validation activities To ensure compilation and maintenance of logbooks for analysis done by HPLC Maintenance of records (user account, service records, sample request of samples) Ard Interested one can share updated resume on Whatsapp at 9915095113 or email at manik.mehta@scllifesciences.com

Position: Research Associate/ Sr. Research Associate, HPLC (API) Note: Candidate should be working in Pharma API industry In ARD Department in HPLC section. Interested one can share updated resume on anuverma@scllifesciences.com or WhatsApp at 9988339860 / 9875994190 Subject matter expert. Through knowledge in theoretical Operational knowledge in handling of Analytical equipment (HPLC, LCMS, Preparative HPLC) Role & responsibilities To perform routine testing of R&D/ PE lab samples in HPLC as per planning. To qualify working standard To maintain and calibrate analytical instruments/ equipment's as per schedule To maintain the good lab practices in ARD Lab To record, process and report data online

Company Name: SCL Lifesciences Ltd. Position: Assistant Manager / Deputy Manager Department: MSTG Location: - Chandigarh COMPANY PROFILE: - SCL Lifesciences Limited is a 30-year-old API manufacturing company with two manufacturing units located in Derabassi five KM from each other -one for domestic supplies and another for exports. We have USFDA, EU-GMP, WHO Geneva, KFTA, PMDA, and TGA, Australia certifications thereby opening the global markets. SCL lifesciences believes in the planet, people, and profits and has a dedicated cell for CSR working in rural schools. It has doubled its profits and turnover in the last three years and is being run by a professional board of both executive and independent directors. Job Summary: As the second in command of MSTG at SCL, you will support the Head of MSTG in overseeing and leading the Technology Transfer and Process Engineering activities within the API manufacturing division. You will assist the ensuring the smooth transfer of technology from development to manufacturing while optimizing process to meet efficiency and quality objectives. KeyResponsibilities:- Technology Transfer: Assist in managing the technology transfer process for new products and process for new products and processes from R&D to commercial production. Collaborate with cross-functional teams including R&D, Manufacturing, Quality and Regulatory Affairs to facilitate successful technology transfer within specified timelines and quality standards. ¢ Contribute to the development and implementation of strategies to mitigate risks associated with technology transfer process. Process Engineering: ¢ Support process engineering activities aimed at optimizing manufacturing processes for efficiency, scalability, and cost effectiveness. ¢ Participate in identifying opportunities forprocess improvements, conducting studies, and implementing solutions to enhance product quality and yield. ¢ Assist in providing technical guidance to the engineering team to drive continuous improvement initiatives. Compliance and Documentation: ¢ Assist in ensuring compliance with regulatory requirements and industry standards throughout technology transfer and process engineering activities. ¢ Review documentation related to technology transfer, process optimization and validation protocols as needed. Cross Functional Collaboration: ¢ Work collaboratively with other departments to facilitate smooth technology transfer and process improvements. ¢ Support Quality Assurance and Regulatory Affairs in regulatory filings and inspections as required. Leadership and Development: ¢ Support Head of MSTG in providing leadership, mentoring and guiding to the MSTG team, promoting a culture of innovation, teamwork and continuous learning. ¢ Identify training needs and development opportunities for team members to enhance their skills and capabilities. Requirements: ¢ A minimum of a B.Tech (Chemical) or M.Tech (Chemical) or a related field is required. ¢ Proven experience (at least 10-15 years) in process engineering and technology transfer in API manufacturing. ¢ Strong knowledge of chemistry, process engineering principles, and pharmaceutical manufacturing processes. ¢ Familiarity with regulatory guidelines and requirements related to APImanufacturing and technology transfer. ¢ Experience in leading cross-functional teams and managing complex projects from development to commercialization. ¢ Excellent problem-solving skills with the ability toanalyze complex issues, identify root causes, and implement effective solutions. ¢ Strong leadership and team management abilities, with a track record of mentoring and developing talent. ¢ Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders. ¢ Detail-oriented mindset, with a commitment to quality, compliance, and continuous improvement.

Role & responsibilities Pharma API Experience Mandatory Qualification: Bsc Fire & Safety/ Eng. Fire & Safety / Msc. Environment Implement and monitor EHS policies, procedures, and practices in line with statutory and company requirements. Conduct safety audits, risk assessments, and HAZOP studies for plant operations. Ensure compliance with environmental norms and health & safety regulations (CPCB, SPCB, Factories Act, etc.). Organize training programs and awareness sessions on fire safety, occupational health, and emergency preparedness. Maintain and inspect firefighting equipment and conduct regular safety drills. Investigate incidents/accidents and prepare root cause analysis reports with corrective and preventive actions. Maintain accurate records of safety permits, incident logs, and environmental reports. Liaise with regulatory authorities and ensure timely submission of compliance documentation. Interested one can share their resume with manik.mehta@scllifesciences.com

Saurav Chemicas Limited is looking for Shift-In-Charge (Production) to join our dynamic team and embark on a rewarding career journey. Oversee production activities during assigned shifts. Ensure compliance with production schedules and quality standards. Monitor and analyze production performance and make improvements as needed. Manage production staff and provide training and guidance. Collaborate with other departments to ensure efficient production operations. Prepare and present reports on production activities and outcomes. Ensure compliance with safety and regulatory requirements.

Position Overview: We are looking for a Sr. Manager will be responsible for leading and managing end-to-end multiple API production blocks. The role requires ensuring optimal productivity, quality, cost control and regulatory compliance in alignment with cGMP standards. This position plays a critical role in driving continuous improvement, cross-functional coordination, and operational excellence within the production unit.. Key Responsibilities: Oversee daily production activities to ensure efficiency, quality, and cost-effective management of resources. Develop and implement production schedules based on inventory / market requirements / capacity constraints and provide feedback accordingly. Deployment of manpower & supervisor as per production requirement. Monitor and adjust production processes as necessary to meet production targets and quality standards. Ensure all production batch records are completed and signed off on time. Responsible or keeping production facilities clean and appropriately disinfected. Responsible for the validation protocols and reports are completed and signed. Responsible for qualification of new and modied facilities, when appropriate and equipment. Responsible for maintaining and updating the documents related to the Production activities. Ensure smooth production under EHS & cGMP compliance. Ensure for reporting of all production deviations and evaluation of the same. Ensure process problems /deviations are solved and rectified within a set of time frame, co-ordination/follow up with all the departments like R&D, MSTG, QC, QA, Engineering & Stores. Institute operational controls, monitor the key characteristics, carry out root cause analysis for the non-conformity and take CAPA. Responsible for self-inspection of the area w.r.t EHS and production systems. Responsible for training all the employees of production. Responsible for preventive maintenance is executed as per the planned schedule. Responsible for analyzing the time cycle of each batch and taking corrective actions if any deviations are observed. Responsible for any optimization initiative across the production blocks. Ensure that the yield, % solvent recovery and quality of APIs and Intermediate products are as per the standard norms. Analyze production costs and recommend strategies to reduce costs and improve Profitability. Responsible for monthly RM requirement and weekly RM schedule. Responsible for performing of Internal audit. Responsible for water consumption, effluent generation as per the set norms. Responsible for controlling hazardous waste generation. Identification of Risks & Hazards, Environmental aspects & evaluation and review the same. Responsible for any other work assigned by senior management in the absence of Site Head/ Unit Head. Qualifications and Experience: Analytical Skills and Communication Basic understanding of pharmaceutical or chemical industry Strong organizational, multitasking abilities, time management skills Company Website :- www.scllifesciences.com

Job description Key Responsibilities: • Conduct organic synthesis experiments to develop and optimize routes for API synthesis. • Design and execute experiments to scale-up synthesis processes from laboratory to pilot plant scale. • Analyze and interpret experimental data to draw conclusions and make recommendations for process improvements. • Collaborate with cross-functional teams including process development, analytical chemistry, and manufacturing to support project objectives. • Maintain accurate records of experimental procedures, observations, and results in accordance with regulatory guidelines. • Stay updated with relevant scientific literature and contribute to the intellectual property portfolio of the company through patent filings and publications. Interested candidates forward resume on anuverma@scllifesciences.com or Whats app/ call on 9988339860.