1376 Hplc Jobs - Page 5

Instrumentation HPLC & GC, LCMS, GMP Knowledge. Perform method transfers, verifications, and troubleshooting in support of process development and scale-up.

Perform analysis using GC, HPLC, UV, KF & wet methods. Ensure GLP, timely reporting, data review, instrument calibration & method validation. Handle OOS, guide juniors & coordinate with QA/production for batch release. Ensure SOP/ISO compliance.

Perform analysis of raw, in-process & finished goods. Operate GC, HPLC, UV, KF, IR. Maintain records, follow GLP & SOPs. Support method validation. Ensure ISO/regulatory compliance & coordinate with QA/production for batch release.

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com . Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azuritys success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. Brief team/department description: The analytical team in Azurity Pharmaceutical is responsible for support of formulation development and related analytical activities for various formulations intended primarily for US market. Principle Responsibilities: Minimum 6 to 8 Years working experience in analytical research and development lab with hands on experience of Method development, Stability analysis in Solid Oral (tablets, Capsules), Oral suspension and Oral solution. Hands on experience on at least HPLC/ UPLC, GC, UV, IR, pH meter, Dissolution, KF titrator etc. Should have potential exposure on method validation/method transfer of different analytical test methods. Good understanding of GLP, GDP, Data integrity and Documentation practices in lab work. Preparation of SOP, Test methods, Validation/Transfer protocols and reports knowledge is added advantage. Good knowledge and exposure on Related test and impurity profile methods development is needed. Knowledge about regulatory requirements on analytical methods, characterization of standards, and impurities is needed. Experience in calibration of different instruments like HPLC, GC, UV, IR, pH meter, Dissolution, KF titrator is required. Qualifications and Education Requirements M.Sc. Chemistry/ Analytical sciences or M. Pharmacy (Chemistry, Analysis or Pharmaceutics By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

Job Description: Role : Executive Analytics Location : Hyderabad Job Purpose/Overview To ensure the Dry Pet Food products leaving the factory operation conforms to the MARS specifications through the assurance of raw materials quality & compliance to process parameters by demonstrating quality inspections, process monitoring & control. The R&D Associate shall assist the Quality & Food Safety In charge in managing the Site Quality Laboratory (Analytical) in terms of executing test plans in timely manner, follow GLP, & cost optimisation. Shall actively participate in design & implementation of QMP (HACCP) Job Responsibilities Coordinate & ensure Proximate profile is tested for Raw Materials, Intermediate and Finished products including new RM, Library samples and Complaint samples on NIR Assist in conducting the testing of Mycotoxin/Aflatoxins analysis using techniques like Chemwell-ELISA, HPLC. Test and release the Packaging Materials according to defined test plan Support to develop and stabilize the analytical techniques in-house as required Coordinate to update and maintain the trend records on different analytical testing s. Manage the consumables for analytical lab and arrange procurement Communicate the release status of received RM, PM and Finished Products to all stakeholders Maintenance of instruments and equipment s related to analytical lab Coordination and execution of third-party testing requirements from different internal stakeholders NIR calibration and maintenance. Support the implementation of Laboratory standard requirements in day-to-day operations in lab by adopting the new procedures and using the new template provided Support Lab & Sanitation Manager via Walk through and Internal audits in the plant and in house laboratory Job Specifications/Qualifications 1. Educational & Professional Qualification MSc Chemistry with first class (or)/ B.Tech Food technology or MSc- in any Life Sciences, with Chemistry as one of the subjects in B Sc. with first class. 2. Knowledge/Experience Minimum 2-3 years working experience in analytical or microbiological laboratory. Working experience with Food/ Pharma Company is preferable.

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 6000 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 70 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compliance and safety requirements. Review of laboratory data, instrument logbook and reports wherever applicable. Initiation of departmental CCRs and tracking the progress to execute the proposed changes through QMS system. Preparation of TAP (Transfer of Analytical Procedures) protocol and Report for various sites. Procuring respective samples and Impurities accordingly. Planning and executing the assigned TAP projects to various sites. Preparation, maintenance and archival of regulatory submission documentation like SOP, protocols, reports for method development and validation. Job Responsibilities Prepares working plan for assigned projects and provides timeline to Manager. Develops stability indicative analytical methods for drug substance and finished product Responsible for all activities in Analytical Development, including cGLP, documentation and implementation of departmental quality systems. Applies AQbD approach to analytical method development where applicable. Responsible for protocol preparation, planning, execution, review and report preparation of various analytical method validation parameters. Ensures analytical methods validation is conducted according to approved validation protocols in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Responsible for method verifications and publishing of analytical methods. Maintenance and archival of analytical method validation documents. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. Raising Change control for various analytical activities (Method SOP and department SOPs) by QMS trackwise To prepare General, Operation and Calibration Standard Operating Procedures. Responsible for initiation, execution and completion of technology transfer and collaborative validation activities of analytical methods to and / or from other departments of Apotex wherever applicable. Responsible for technology transfer and Transfer of analytical procedures activity to support the supervisor. Communicating the requirements for the Leaders and within the team members for effective cGLP procedures and departmental quality systems to achieve all outcomes. With minimal guidance, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. To participate in the mandatory trainings to execute the day to day job responsibilities. Assist in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GLP. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Practice and up-gradation of knowledge with respect to cGMP. Performs all work in accordance with all established regulatory and compliance and safety requirements. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Performs the calibration of instruments in Analytical R&D and ensures the compliance as per cGLP requirements. Work as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education A graduate/post graduate in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, UV, IR spectrophotometer and dissolution apparatus, wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge on preparation and review of various documents like SOPs, Formats, Protocols, Reports, analytical data, investigation and deviation reports. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities Should possess troubleshooting knowledge on Instruments and analysis. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 4 years or PhD with 2 years experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Must Abide by the rules & regulations of the laboratory. Responsible for Performing tests as per authorization and ensuring the TAT Compliance. Ensure Safe Handling of Equipment’s. Filling all logbooks for the equipment’s as per usage Ensure to wear all the PPE’s and lap aprons before performing the tests without fail. Ensure to follow safety rules & Maintain 5S. Pesticides & Mycotoxins analysis in food & agriculture as per authorization. Follow ISO 17025 requirements in lab with respect to Quality compliance and other regulatory requirements. Internal calibration of equipment’s Maintenance. Handling, Operating & Calibration, Maintenance of LC MSMS. Handling, Operating & Calibration, Maintenance of GC MSMS. CRM Management, Preparation, Storage, Disposal and Record maintenance. Roles and Responsibilities • Must Abide by the rules & regulations of the laboratory. • Responsible for Performing tests as per authorization and ensuring the TAT Compliance. • Ensure Safe Handling of Equipment’s. • Filling all logbooks for the equipment’s as per usage • Ensure to wear all the PPE’s and lap aprons before performing the tests without fail. • Ensure to follow safety rules & Maintain 5S. • Pesticides & Mycotoxins analysis in food & agriculture as per authorization. • Follow ISO 17025 requirements in lab with respect to Quality compliance and other regulatory requirements. • Internal calibration of equipment’s Maintenance. • Handling, Operating & Calibration, Maintenance of LC MSMS. • Handling, Operating & Calibration, Maintenance of GC MSMS. • CRM Management, Preparation, Storage, Disposal and Record maintenance.

1. Supervise end to end operations of food Chemical lab maintain the TAT for all the samples. 2. Implementation of Quality System as per all applicable accreditations like ISO 17025, FSSAI, EIC, APEDA etc. 3. Maintain all relevant documentation and presents as needed for quality audits and Regulatory audits 4. Implementation and Complying to the other TUV SUD Process and Policies 5. Implementation of good laboratory practices 6. Ensure on time method development / verification and validation 7. Implementation of any new process as decided by the management 8. Monitoring the turnaround time of the sections / reports as per the given schedule 9. Testing capability confirmation to sales and co-ordination with sales team for smooth lab operation. 10. Immediate response to internal or external enquiries. 11. Implementation of the safety guidelines for the respective areas 12. Minimize wastages inside the laboratory 13. Support in data inputs for new investment planning 14. Regular employee engagement 15. Driving continual improvements projects 16. Monitoring Expenses and take the required actions as on required 17. Coordinate and ensure Calibration / Preventive Maintenance / repair schedule with adequate documentation. 18. Equipment /method troubleshooting / repairs 19. Shift management and leave Management of the lab team 20. Supporting technical manager for RCA and CAPA 21. Ensure on-time training of respective team as per training planner Roles and Responsibilities 1. Supervise end to end operations of food Chemical lab maintain the TAT for all the samples. 2. Implementation of Quality System as per all applicable accreditations like ISO 17025, FSSAI, EIC, APEDA etc. 3. Maintain all relevant documentation and presents as needed for quality audits and Regulatory audits 4. Implementation and Complying to the other TUV SUD Process and Policies 5. Implementation of good laboratory practices 6. Ensure on time method development / verification and validation 7. Implementation of any new process as decided by the management 8. Monitoring the turnaround time of the sections / reports as per the given schedule 9. Testing capability confirmation to sales and co-ordination with sales team for smooth lab operation. 10. Immediate response to internal or external enquiries. 11. Implementation of the safety guidelines for the respective areas 12. Minimize wastages inside the laboratory 13. Support in data inputs for new investment planning 14. Regular employee engagement 15. Driving continual improvements projects 16. Monitoring Expenses and take the required actions as on required 17. Coordinate and ensure Calibration / Preventive Maintenance / repair schedule with adequate documentation. 18. Equipment /method troubleshooting / repairs 19. Shift management and leave Management of the lab team 20. Supporting technical manager for RCA and CAPA 21. Ensure on-time training of respective team as per training planner

Job Title: Invitro BA Scientist Job Location: Bangalore, Hyderabad' About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines • Overall adherence to safe practices and procedures of oneself and the teams aligned • Contributing to development of procedures, practices and systems that ensures safe operations and compliance to companys integrity & quality standards • Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. • Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. • Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self • Compliance to Syngene s quality standards at all times • Hold self and their teams accountable for the achievement of safety goals • Govern and Review safety metrics from time to time Core Purpose of the Role : • To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment • Processing of different matrices samples of PK studies • Optimization of test compounds manually as well as automated on LCMS/MS • Develop methods with the team lead • Independently handling of HPLC for UV based samples analysis. • Documenting the lab note books online and compound management Syngene Values All employees will consistently demonstrate alignment with our core values ' Excellence Integrity Professionalism Experience 3- 10+years Education : Msc/Pharm/Mtech/Phd/ Fresh phd with relevant exp during academics or any postdoc Skills and Capabilities • Expertise in column selection, mobile phase selection, solvent preparations and sample processing techniques such as protein precipitation, liquid-liquid extraction and solid phase extraction is mandatory • Sample processing of New chemical entities from various in-vitro and in-vivo studies executed in Preclinical discovery by using appropriate extraction methods • Should be able to develop and validate LC-MS based qualitative/quantitative methods and apply them in routine analysis • Should be well versed with internet-based literature search and capable of implementing the Learnings as and when required • Candidate is expected to have basic understanding in interpretation of Mass/UV Spectra • Should ensure preventative maintenance and calibration schedules of HPLC & mass spec by coordinating with vendor and support staff • General understanding of Drug metabolism and Pharmacokinetics • Should be able to deliver scientific presentation in departmental journal club and write official Project reports

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 25-07-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 25-07-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

Role & responsibilities Biological (Therapeutical Protein) sample analysis by HPLC, UV, pH meter, Osmometer, ELISA and SDS-PAGE methods. Calibration of instruments and equipment as per the SOP. Responsible for analysis of in-process, finished products and stability samples. Raw material sampling and outsourcing activity. Preparation of certificate of analysis. Preparation of standard operating procedures, specifications, Protocols and standard testing procedures Operation of High Performance Liquid chromatography, UV spectrophotometer, Osmometer, pH Meter, gel power pack, Plate reader and stability chambers. Initiation of QMS events like lab event, Deviation, OOS, CAPA and Change controls Daily Maintenance of QC laboratory as per GMP requirement. Supervision of AMC and CMC activities for all instruments in the QC. Work in Shifts Preferred candidate profile

As a Senior Chemist at Scimplify, located in Kurkumbh, Pune, you will be responsible for various tasks related to sampling and analysis of raw materials, packing materials, and finished goods. You will be required to conduct analysis of finished products, in-process samples, stability samples, raw materials, and packing materials. Your role will also include maintaining and calibrating various lab instruments such as HPLC, Gas Chromatography, Karl-Fischer Titrator, Melting-Boiling Point Apparatus, Refractive Index, Moisture Analyzer, pH meter, and Weighing Balance. It is essential to work in compliance with approved methods, SOPs, cGMP, and CGLP standards. Additionally, you will be responsible for proper documentation of laboratory data and generating complete testing reports for in-process samples, finished products, and stability samples. You will also be involved in instrument handling, specifically with instruments like HPLC-Shimadzu-LabSolution, Gas Chromatography-Young Lin 6500-YL Clarity, Karl-Fisher Titrator-Spectra lab, Melting Boiling Point Apparatus-Spectralab, Moisture Analyzer-Mettler Toledo, Refractometer-ABBE, Way2s, Weighing Balance-Mettler Toledo, and pH Meter-Spectralab. As a Senior Chemist, you will play a crucial role in ensuring the accuracy and reliability of the analytical results while adhering to the quality standards set by the organization. Your contribution will be vital in maintaining the high-quality standards of the products manufactured by Scimplify.,

Conduct quality control tests on API samples using various analytical techniques such as HPLC, GC, UV, etc. Method Verification, Calibration

Role & responsibilities Good experience in LC-MS. API candidate apply for this position Preferred candidate profile Male candidate only

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey Ensure smooth execution of operational and administrative tasks Support management in compliance, reporting, and daily operations Monitor work processes and suggest efficiency improvements Maintain accurate documentation and uphold company policies

Should be capable of handling wet analysis like LOD, Ash content, Moisture content analysis etc Should have the knowledge of instrumentation analysis like HPLC , GC , IR , UV , Titrator etc,, Should have knowledge of GLP , GDP and GMP

Should be capable of handling instrument like HPLC, GC , UV, IR and potentiometry Should have the GMP knowledge and compliance requirement of QC Should have the knowledge on Good laboratory practices .

Analytical test including physical and wet analysis. Expertise in handling of HPLC, GC , UV and IR Knowledge on OOS and OOT Calibration of laboratory Instruments. Preparation and standardization of Reagents/Volumetric solutions. To ensure cGLP compliance and Data Integrity

Role & responsibilities Required for Quality Control(Formulations) Quality Control(QC)- Need 1 to 5 years of experience. *Analysis of Finished Product & Stability *GLP and LIMS, Documentation Preferred candidate profile Perks and benefits

Good technical knowledge of analytical techniques and instrumentation: Chromatography technique like High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC), Spectroscopy technique like UV-Vis and Infrared (IR), KF titration, zettaliter, Osmometer and Dissolution etc Skills in developing, optimizing, and validating analytical methods to ensure accuracy, precision, and reliability. Understanding of Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Data integrity and relevant regulatory guidelines (e.g., ICH, FDA, EP) to ensure compliance. Should have strong strong understanding & experience in injectables is mandatory Immediate joiners preferred Email : monisha.lahiri@randstad.in

Aster Medcity is looking for Executive.Finance & Accounts to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

Preferred Education/ Qualification:- B.Pharm/M.Pharm/M.Sc Experience:- 4 6 years of experience in Quality Assurance / Quality control . 1. Responsible to review the Quality control documents. 2. Fundamental knowledge on Quality control activities. 3. Technical document review skills. 4. Handling of change control assessment and approval 5. Interpersonal Skills: Effective communication with all staff from different levels and builds constructive and effective relationship. 6. Acts Decisively: Makes decision in a timely manner based on available information 7. Grows Self: Identify Individual development needs and create a plan and work towards achieving those objectives 8. Critical thinking and Compliance mindset. 9. Good performance, partially independent, reviews trends and data. 10. Responsible for review of Quality control documents (Analytical Method Validation documents, SOPs, Forms, Stability documents review and approval. Stability trend data and etc.,) to meet current regulatory requirements. 11. Coordinating with CFT for addressing & resolving of Review Comments for timely Closure. 12. Should have trouble shooting abilities in quality control area, which helps the organization to develop, implement and achieve its mission, vision and values. 13. Identify gaps and involve in Process and Procedure Simplification, thereby reduce downtime and increase the Efficiency. 14. Report any non-compliance to the Supervisor 15. Should be aware of operation of eQMS change Mangement process. 16. Basic knowledge on gLIMS, SAP, EDES, EAMS. 17. Basic knowledge QRA process. 18. Experience on handling of HPLC, GC, ICP-MS and other instruments. 19. Critical thinking to identify the potential issues in the process. 20. Good to have yellow belt certification. Work Location Assignment: On Premise Quality Assurance and Control #LI-PFE

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy. What You Will Achieve In this role, you will: Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Perform testing on various samples, manage Laboratory Information Management System builds. Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues. Here Is What You Need (Minimum Requirements) Batchlor of Science/ Pharmacy or Master of science / pharmacy with 1 to 6 years of quality control experience Strong technical skills chemical quality testing Detail-oriented with robust knowledge of quality control process Familiarity with analytical laboratory equipments like HPLC, GC, AAS,ICP-MS, UV, IR and etc., Effective written and verbal communication, as well as interpersonal skills Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical experience Experience with Laboratory Information Management Systems (LIMS) Knowledge of regulatory requirements and guidelines Strong problem-solving abilities Effective time management and organizational skills Ability to mentor and train junior colleagues Work Location Assignment: On Premise Quality Assurance and Control #LI-PFE

Oversees QC activities, staff training, SOPs, calibrations, GLP compliance, audits, records, and lab investigations (OOS/OOT) and aligns QC goals with production and ensures lab standards (candidates having approval from Raj. FDA will be preferred).

Role & responsibilities Literature survey report preparation. Expertise in an API Synthesis. Organize for relevant patents and papers from literature Organize / order raw materials / chemicals from different vendors / plants Develop a most economical / eco friendly commercially viable technology at bench scale APIs by effective use of sustainability tool & Statistical (DOE) tools. Participating in cross-functional project teams and contributing to scientific strategies and goals. Presenting data and reports on project status at meetings. Contributing to the development of new peptide-based technologies. Adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Troubleshooting and maintaining peptide synthesis equipment. Participating in optimization and automation improvements for enhancing peptide synthesis capacity. Maintaining a clean and organized laboratory environment. Strong proficiency in solid-phase peptide synthesis, analytical techniques (HPLC, LC-MS, NMR), and data analysis. Excellent communication, teamwork, and problem-solving skills are essential. Familiarity with laboratory safety protocols and regulatory guidelines is also important Daily experimental planning, execution, recording & data Compilation To meet EHS and compliance expectation Supporting/report preparation of Genotoxic & nitrosamine impurities To prepare reports such as safety, vendor qualification reports, Supporting/Preparation of Process development report, ACMI report Technology transfer and piloting of developed peptides RMC sheet preparation Competencies required Sound knowledge of organic chemistry, Spectroscopy, Drug Regulatory Affairs & Quality Assurance ICH Guidelines and basic IP understanding Good experimental hand & Scale-up knowledge Innovative thinking & excellent observance Note - API experience is mandatory. Interested candidate can share their profile on jasleen.kaur@tapi.com or connect on 8076954558.