123 Ftir Jobs - Page 3

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Division :- Formulation Interview Date:- 05-04-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

We have been retained by a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development to hire a "Junior GMP Consultant - QC & QA" to be based at their HO located at Navi Mumbai. Details of the position are mentioned below: Company: Our Client is a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development. They have their head office in Mumbai and subsidiaries in Europe, Singapore, Australia and Malaysia. They have been providing high quality & credible consulting services to the Pharmaceutical Industry in India and internationally. They have a young and committed team of GMP and Regulatory Experts. Role & responsibilities: Adequate experience and well versed with Quality Control and Quality Assurance systems and procedures in accordance to regulatory standards. Hands on experience in handling HPLC, GC, UV, FTIR, etc., worked on LIMS, audit trail, CSV , familiarity with GMP, GLP, EUGMP and ICH guidelines, Should have exposure working in formulations like oral solids dosage form (OSD), injectables, etc. Experience: Min 5-10 years experience in quality control & Quality Assurance in pharmaceutical industry. Knowledge & Skills Candidate should have exposure working in QC/QA laboratory in Regulated companies. Well versed with Quality Management systems/procedures Thorough knowledge of testing Raw materials, finished product, Packing materials and handling of key instrumentation like HPLC (auto sampler), GC, dissolution testing. Well versed with QC systems & procedures, audit trail review of HPLC, GC and have knowledge of computer system validation related to QC instruments. Familiarity with GMP, GLP, EUGMP and ICH guidelines. Familiar with stability management and calibration Well versed in carrying out Analytical Method validation/verification, Analytical tech transfers. Fluency in English and good communication written and verbal. Job responsibility: 1)To assist project lead in reviewing the QC systems, documentation and practices for client. 2) Participate in Supplier audits at various sites 3) Maintaining GMP data base and preparation of SOPs 4) Ready to do extensive travelling to visit Client sites and supplier audits (domestic & international) Preferred candidate: Candidates based only in Mumbai/Navi Mumbai will be preferred. 6. Qualifications: Education: A masters degree in Pharmaceutical Sciences or a master's degree in Analytical Chemistry Skills and Competencies: Strong analytical and problem-solving skills. Attention to detail and accuracy in testing and documentation. Proficient in the use of laboratory equipment and software. Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated CV to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak, Director, Pharma Placements Inc. Mobile: 98202 34987 / 81307 24980

Position: Trainee - API Quality Control Experience Required: 0-1 Year (Freshers Welcome!) Key Responsibilities: Understanding Quality Control Basics - Introduction to GMP, GLP, and Data Integrity. Sampling Handling of Raw Materials, In-Process, Finished Products. Performing Basic Wet/Chemical Analysis - Assay Titration, Loss on Drying (LOD), Sulphated Ash. Preparation of Volumetric Solutions Standardization. Basic Instrument Handling - FTIR, UV, and pH Measurement. Learning Assisting in Documentation - Lab Records Analytical Reports. Ensuring Compliance with Regulatory Requirements. Required Skills: Strong interest in analytical chemistry laboratory techniques Understanding of basic quality control parameters Eagerness to learn pharmaceutical industry standards Why Join Us Structured training mentorship programs Career growth opportunities within QC Analytical Research Competitive compensation benefits

Key Responsibilities: Perform Routine Wet Chemical Analysis - Assay Titration, Loss on Drying (LOD), Sulphated Ash, pH Measurement, Solubility Testing. Instrumental Analysis - Hands-on experience with FTIR, UV, HPLC, GC, and Auto Titration. Sampling Testing of Raw Materials, In-Process, and Finished Products. Preparation Standardization of Volumetric Solutions. Review Maintenance of Analytical Documentation - Analytical Reports, Logbooks, and COAs. Conduct Stability Studies Method Validations. Basic Troubleshooting Calibration of Analytical Instruments. Ensure Compliance with GMP, GLP, and Regulatory Requirements. Required Skills: Strong understanding of wet instrumental analysis. Hands-on experience in Analytical Techniques - FTIR, UV, HPLC, GC, Auto Titration. Knowledge of Regulatory Guidelines - ICH, WHO, FDA, EU-GMP. Understanding of Quality Management Systems (QMS) Data Integrity. Ability to handle Out of Specification (OOS) Out of Trend (OOT) investigations. Good communication documentation skills.

Lead the Quality Control team to ensure bromine products meet regulatory & quality standards. Develop & implement quality control protocols, conduct complex chemical analyses, and troubleshoot quality issues Implement strict QC control, documentation Required Candidate profile Work in a laboratory environment with personal protective equipment (PPE). Physical stamina for standing, walking, and lifting Documentation, Independent Lab supervision & strict QC control

Dear All, We have opening in our esteemed organization as Service Engineer. Position: Service Engineer Company Name: MSP Lab Instruments Pvt Ltd No of Positions: 05 Experience: 2+ Years of experience Qualification: Diploma/B.Tech/M.Sc Electronics or Instrumentation Location: Pune/Bangalore Salary Negotiable: Job description Performing preventive maintenance of analytical instruments like HPLC, GC, FTIR, UV visible spectrophotometer, dissolution apparatus, weighing balances, titrators. Handling breakdowns of above analytical instruments. Capillary electrophoresis system HPLC (Agilent_Open lab, Waters_Empower-3) PA 800 plus (Capillary Electrophoresis) Software_32 karat UV-Spectrophotometer ELISA Reader and Washer Gel electrophoresis KF Autotitrator and Coulometer pH meter Osmometer Kjeldahl Nephelometer Automated coagulometer TOC Weighing Balance Share your resumes to hr@msplabinstruments.com

Analysis of API/ excipients finished product and in-process samples with peer review. Method Development Calibration and maintenance of analytical instruments General lab responsibilities as decided by HOD. Following in-house compliance system Maintain hygienic condition in respective department. Follow GxP (GMP, GDP, and GLP) for all processes. Ensure use of Personal Protective Equipment attend EHS training send waste to concerned person comply EHS requirements. All projects TRF management, segregation, and entry. Working standard/ impurities management Ensure data integrity. M.Sc/M.Pharm

Job Title: Analyst Department: ECOLAB Job Includes: 1. Have knowledge of Instrument like HPLC, UV-Visible Spectrophotometer, GCMS, GCMS-Headspace, ICP-OES, LCMS-MS, FTIR, DSC. 2. Daily routine analysis of sample as per SOP / ISO Methods. 3. To maintain good laboratory practices and use of PPE in lab. 4. Analysing and interpreting data results. 5. Routine Maintenance and Calibration of all Analytical Instruments and trouble shooting. 6. To do NABL Document related work as per schedules. 7. Have Knowledge of Method Development and Method Validation as per ISO 17025. 8. Preparation of CRM (Certified reference material) and documentation of records 9. To maintain the stocks of Cylinder, Chemicals and Standards stock 10. Other support functions as and when required Experience: 1. BSc. or MSc. in chemistry 2. Good Interpersonal skills and co-ordination and co-operation. 3. Understanding the instruction of Supervisor and Exchange of Basic Information.

Description Vantive: A New Company Built on Our Legacy Since last year, we have been on a journey to separate our Kidney Care segment into a standalone company. Vantive will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don t settle for the mediocre. Each of us are driven to help improve patients lives worldwide. Join us as we revolutionize kidney care and other vital organ support. Job Summary Job Title - Principal Eng, Containers (Renal, Containers) Location - Whitefield, Bangalore Shift - General Job Responsibilities: Will be responsible for product R&D and analytical activities in order to execute global, cross-functional projects pertaining to polymeric materials Should have a good understanding of polymer science & polymeric composites, be able to study their structure-property relationships and have an ability to understand chemical analyses data from methods such as, FTIR, NMR, ICP-OES etc., along with understanding of mechanical testing of materials, such as, tensile testing etc. Will work with senior members of the team e.g. SME & manager to carry out root cause analyses in case of product failures with minimal supervision Will be responsible for project management which includes managing change controls -using Vantive s in-house quality systems like TW8, TcU Will work with senior members of the team e.g. SMEs and manager for writing of verification/validation test protocols (mechanical &/or chemical/material characterization), test cases and documenting results in the form of technical reports The role would involve preparing and presenting technical work and deliverables to the global project team(s) in a well-planned manner with a clear logical flow Will be able to leverage own expertise as well as inputs from others to identify and resolve critical issues Will perform troubleshooting and problem-solving related to material aspects of the products associated with field performance and manufacturing Qualifications PhD degree in a relevant discipline or Masters degree in Polymer Science/Polymer Engineering or closely related disciplines Minimum 9 years of relevant work experience in the field of Polymer Science & Engineering with an experience in manufacturing - especially in medical devices or pharmaceuticals - being an added advantage Clear and effective communication (written, oral) and presentation skills. Good stakeholder management (local and global) A proven track record of effectiveness in a fast-paced environment. Proven ability to create results within budget, timeline, and product/project deliverables Skills Excellent English verbal and written communication skills 1+ year of Project management experience experience (Academic &/or industrial) with polymeric materials testing methodologies, such as, FTIR, GC-MS, HPLC, tensile testing etc. Solid computer skills: email, documentation, and collaboration tools: e.g. WebEx, Teams, Microsoft Office products, etc. Self-directed, resourceful, and able to work on multiple projects and priorities. Strong organization, attention to detail, and documentation skills. Demonstrated experience in solving complex technical problems using root-cause analysis techniques. Hands on experience in polymeric material s testing is an added advantage Ability to objectively identify technical solutions Recruitment Fraud Notice

RESPONSIBILITY : Analyze Finished Product/process validation samples/Stability/Swab sample and Raw Materials allotted for testing using HPLC, GC, Dissolution Rate apparatus, FTIR, UV, KF, and DT Apparatus etc. Tablet hardness tester, Friability apparatus and Loss on Drying (LOD), etc. as per Stability protocol and Test procedure. Recording and calculation of analytical data. Destruction of left over samples and expired Raw materials. Enter analytical data in SAP and generate COA (Certificate of analysis data). To follow compliance to cGMP requirements and laboratory procedures for integrity, accuracy and adequacy of the analysis performed. Analysis and reporting as per work allotment and hand over analytical reports to lab in-charge/reviewer at the end of the shift. To follow E. H. S (Environment, health and safety) policies. Timely inform the lab in charge or manager about any Lab event, OOS/OOT and deviation. I

Role & responsibilities Experience in operation and trouble shooting of process in plant. Isolation and purification of different organic compound using column chromatographic and crystallization techniques. Optimize the process parameters, what-if studies, holding studies etc. for scale up. Investigation of OOS/OOT and stability related issues. Analytical development In R&D department Reactions performed like Hydrogenation, Brominating, Oxidation, Reduction and condensation. Handling of Moisture sensitive reactions. Study and understand the project requirements, identifying and collection of suitable literature. Support lab manager to prepare weekly technical reports and other project related technical documents (impurity profile tables, Plant batch data, developmental reports) Executing assigned reactions of project. • Looking after the Safety equipment's management and maintaining it as per regulatory requirement in R&D lab. • Study the MSDS of each chemical using in every new project and make arrangement of Safety equipment's accordingly. Handled HPLC system of Agilent technologies Eriochrome (A.04.07) and version Open Lab cds2.4 • Good in Thin layer chromatography & Column chromatography. • Polymorph characterization with the aid of XRD, DSC, TGA and IR Techniques. • Having good ability to interpret analytical results like NMR, HPLC, GC, LCMS, MASS, IR & UV. Preferred candidate profile Perks and benefits

Description TM/CM/XPS Overal 5-6 years SAP experience Should have 2-3 years experience on either SAP TM / Assist4 or XPS Configure TM system settings, master data, transportation networks, carrier data and relevant business processes Worked on EDI/API integrations with Third party Interfaces in Outbound delivery processed Customize and enhance SAP TM functionalities through appropriate extensions, integrations and enhancements Collaborate with business stakeholders to analyze the transportation management needs and translate them into effective TM solutions Knowledge of Supply Chain Management processes particularly transportation and logisitcs Work with third party-party systems and interface as necessary Integrate TM with other SAP modules (e.g. ECC, EWM) and third party systems to create a seamless supply chain solution Should have 2-3 years experience on either SAP TM / Assist4 or XPS Positive attitude and zeal to learn is a must requirement. Should have 2-3 years experience to work on enhanacement or implementation project Should have good experience to have worked on waterfall methodology Additional Worked on ALE/EDI/Idoc integrations with Third party Interfaces in Procurement and Production warehouses Extensively Worked on Smart forms, integration technologies with Printer configuration along with Basis teams Worked on RF configuration in integration with Barcode Technology Worked on all RICEFS components. Named Job Posting? (if Yes - needs to be approved by SCSC) Additional Details Global Grade C Level To Be Defined Named Job Posting? (if Yes - needs to be approved by SCSC) No Remote work possibility No Global Role Family To be defined Local Role Name To be defined Local Skills SAP Transportation Management Languages RequiredENGLISH Role Rarity Niche

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-29-03-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Hands on experience in operation of analytical instruments like HPLC, GC, Dissolution, PSD, ICP-MS, XRD Good skill in documentation of the activities performed as per GLP Hands on experience on calibration of analytical instruments Adequate knowledge on analytical method validation and method transfers

Should have 3-7 years’ experience in Quality control Testing of Raw materials and Finished products Testing of stability samples Handling of HPLC & GC instruments Handling of Chromeleon software Handling of UV, TOC, FTIR & Auto titrator instruments Instrument calibrations & trouble shooting Handling of LIMS Should have knowledge on GMP/GLP Should have knowledge on OOS/OOT/Deviations/Laboratory incidents

Assistant Manager: Job Description: We are looking for a highly motivated and skilled Assistant Manager withstrong domain knowledge in Data Analysis / Business Analysis to join ourgrowing team. Responsibilities: Demonstratestrong analytical and statistical skills towards taking complex businessproblems, wide variety of quantitative data, and provide structured anddata-supported practical solutions towards optimizing shipping problems. Serve as atrusted partner to business units, translating complex analytical results intobusiness insights, create necessary tools/reports to monitor and ensure programsuccess. High levelof attention to detail to ensure accuracy in data analysis and documentation. Proventrack record of using analytics to drive significant business impact, creatingdeep-dives and presenting work efficiently. Skills: B.Tech in aquantitative field like Engineering, Computer Science, Mathematics etc. 3-5 yearsof experience, at least 3 years of relevant analytics experience Stronganalytical skills with expertise in SQL, and Excel. Proficiency in astatistical programming language like R or Python would be a plus. StrongProblem-solving skills with the ability to interpret complex data sets. Goodcommunication skills, with experience working in a fast-paced environment withcross-functional teams. We are an equal opportunityemployer and value diversity at our company. We do not discriminate based onrace, religion, colour, national origin, sex, gender, gender expression, sexualorientation, age, marital status, veteran status, or disability status.

Key Responsibilities: Perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished products using various laboratory instruments (e.g., HPLC, GC, UV-Vis, FTIR). Calibrate, maintain, and troubleshoot laboratory instruments to ensure accurate and reliable results. Prepare and review Standard Operating Procedures (SOPs) for analytical methods and ensure compliance with quality standards. Analyze data from testing and document results in reports, ensuring proper record-keeping and traceability. Conduct stability studies and product testing to ensure that products meet specifications. Work closely with production teams to resolve any quality-related issues and recommend corrective actions. Assist in the development and validation of new analytical methods. Ensure compliance with Good Laboratory Practices (GLP) and relevant regulatory requirements (e.g., GMP, ISO). Perform equipment maintenance and troubleshooting to ensure continuous operation of testing instruments. Assist in the preparation for internal and external audits and inspections. Qualifications: Bachelors degree in Chemistry, Biochemistry, or a related field. Proven experience (2+ years) in a Quality Control role within a laboratory or pharmaceutical/chemical industry. Familiarity with lab instruments such as HPLC, GC, UV-Vis spectrophotometer, and other analytical techniques. Strong understanding of GLP, GMP, and regulatory standards. Excellent attention to detail and ability to work independently. Strong analytical and problem-solving skills. Good communication and documentation skills. Ability to work under pressure and meet tight deadlines.

Role & responsibilities Responsible for microbiology lab activities & compliance Environmental Monitoring Risk Assessments/ rationales and area qualification Ensuring timely release of all microbiological tests thereby meeting company targets Handling of QMS activities like Change Controls, Incident, OOS and OOL investigations and impact assessments Review/ approval of protocols and reports of analytical method development, method suitability studies, process validations, Instruments/equipment qualifications and various miscellaneous microbiological validation/ activities and analytical documents Responsible for participation / evaluation of Risk Assessments/ impact assessments wherever applicable Review/approval of trends as applicable and to recommend any changes for the better control of the system Responsible to handle internal and external audits and coordinate with all cross functional teams for better productivity and quality Responsible to take the lab rounds on daily basis and correct the non-compliance if found any and to find out the opportunities for improvements Improvement of quality culture in the team and ensuring the safety in the lab Ensuring the compliance to Audit observations related to microbiology Regular updates to QC Head about incidents, OOS and CAPA's To ensure strict adherence to safety & cGMP all factory and maintain the data integrity in the microbiology lab Ability to work independently and as part of a team Preferred candidate profile Candidates with minimum 8 - 12 years experience from Pharmaceutical industry (formulation / topical background preferred)

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications. Perks and benefits: Mention available facilities and benefits the company is offering with this job.

Perform analytical method development, method validation and query response for the finished product. Prepare analytical method development reports, CDP and COA (Certificate of Analysis) Perform and review analysis of In-process sample/Finished goods/ Stability samples and related documentation as per cGMP requirement. Monitoring general laboratory and its maintenance activity as applicable. Responsible for performing routine analysis and stability analysis of the finished product for assay, CU, related substances, dissolution and residual solvent etc. Prepare draft STP. Review of analytical data, calibration data and qualification data Responsible for troubleshooting and maintenance of HPLC, GC, UV/Visible and spectrophotometer etc. Calibration of analytical instruments like Analytical Balance, pH meter, UV spectrophotometer, KF Potentiometer, Karl Fischer as per the schedule. Following in house systems and procedures to ensure cGMP practices and regulatory requirements. Maintenance of reference standard, working standards and their standardization. Co-ordinating the activities in Chemical and Instrumentation. Handling of Troubleshooting. To update instrument log book entries Desired Skills: Must have experience in formulation testing in reputed pharma organizations. Handling of instruments like HPLC, GC, UV, UPLC, Dissolution tester, KF, FTIR. Strong knowledge of Microsoft Word/Excel.PPT. Good Communication and problem solving skills. Should be assertive, proactive and self-driven. Should be willing to work in a dynamic work environment. Pedigree: B. Sc (Chemistry), M.Sc (Chemistry) with 3-5 years of relevant work experience.

- Perform daily activities for failure analysis (FA) for advanced technology nodes collaborating with different FA labs - Develop a Failure analysis ecosystem in India for various materials, applications and defects collaborating with Apple labs across geographies - Conduct physical fault isolation using various FA tools - Develop comprehensive FA methodologies for failures on metals, plastics, polymers, glass and other types of raw materials - Prepare technical reports / presentations summarizing failure analysis findings recommend improvements in production processes - Analyzing experimental data to provide in-depth understanding of design features manufacturing process nuances - Researching innovative technology to understand root causes of different types of cosmetic defects, reliability and dimensional failures on different components - Providing process improvement direction to multi-disciplinary teams to improve product quality, reliability, part cosmetics, bonding performance of components. - Interacting with a diverse and passionate group of team members to communicate results and provide clear and first principles driven direction based on failure analysis - Tackle new challenges everyday both technical and logistical, where your contributions will drive improvements to the product. - Manage Quality functions for some metal processing like billet manufacturing, extrusion etc Minimum Qualifications Minimum Qualifications 8+ years of expertise in failure analysis methodology to identify root cause Ability to make clear and concise slides/ presentations through Keynote, Excel, etc. Demonstrate an unwavering passion for engineering products with exceptional reliability Expertise in Failure Analysis techniques (Optical Microscopy, FTIR, X-ray/CT, Scanning Electron Microscopy/Energy Dispersive Spectroscopy, EBSD etc.), and the ability to use failure analysis methodology to derive a root cause of failure Bachelor s degree in engineering (mechanical, materials, etc.). MS/ME or PhD in Mechanical, Metallurgical Engineering with industry experience preferred Key Qualifications Key Qualifications Preferred Qualifications Preferred Qualifications Excellent written and verbal communication skills for audiences ranging from technicians to senior executives Experience in spirited collaboration between multidisciplinary teams of engineers and scientists to solve complex electromechanical / mechanical design challenges Ability to travel internationally without restriction Collaborative attitude and ability to cross-functionally work effectively Education Experience Education Experience Additional Requirements Additional Requirements More

Company: Strides Pharma Department: Quality Control Position: Executive Job Location: KRSG Plant, Alathur Qualification: M.Sc. (Chemistry), B-Pharm, M-Pharm Experience: 2 to 6 Years Key skills: • Analysis of Material / Product by referring current version of specification STP with relevant material code. • Responsible for initial set up of Instrument/Equipment before starting the analysis with relevant online entries in usage • Log / LIMS. • Perform the Assay and RS by LC/UV/Dissolution, content uniformity by LC analysis with simple and complex products • Tests as per SOP/STP. • Proper handling of chromatographic column used for analysis. • Maintain data integrity and appropriate traceability

Handling of HPLC Handling of GC Handling of UV.Vis Spectrophotometer

TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industrys broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in RD generates a steady flow of APIs, enabling timely introduction of new products to market. How you ll spend your day Excellent communication and with hands on experience. Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets. Troubleshooting/OOS investigations during validations. Having a good knowledge of HPLC, IR, UV, KF Titrator, Halogen Moisture analyzer, Polarimeter and wet analysis Having good knowledge of HPLC trouble shooting. Sound knowledge of Organic Chemistry Spectroscopy. Having a good knowledge of HPLC Method development of API/RM/KSM and SM using various detector like Mass, IR, CAD, ELSD, UV-PDA and UV. Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques. Data interpretation by NMR, Mass Spectrometer, DSC, TGA FTIR Having a sound knowledge of Analytical method validation. Hands on experience of various Analytical Instruments-Coulometer, FT-IR, UV, Karl Fisher, Halogen Moisture Analyzer etc., >sound knowledge of Organic Chemistry Spectroscopy. Your experience and qualifications MSc (Organic chemistry/Analytical chemistry) 4- 7 year

Find endless opportunities to solve our clients toughest challenges, as you work with exceptional people, the latest tech and leading companies across industries. Practice: Strategy & Consulting, Global Network I Areas of Work: Cost takeout, earnings before interest, taxes, depreciation, and amortization, (EBITDA) improvement in Direct Spend | Level:Consultant | Location: Delhi, Gurgaon, Mumbai, Bangalore, Pune, Hyderabad| Years of Exp:4-8 years for Consultant, 1-4 years for Analyst Explore an Exciting Career at Accenture Are you an outcome-oriented problem solver? Do you enjoy working on transformation strategies for global clients? Does working in an inclusive and collaborative environment spark your interest? Then, Accenture Strategy and Consulting is the right place for you to explore limitless possibilities. As a part of our Cost & Productivity Reinvention (C&PR) practice, you will help organizations reimagine and transform their supply chains for tomorrow"”with a positive impact on the business, society and the planet. Together, let's innovate, build competitive advantage, improve business, and societal outcomes, in an ever-changing, ever-challenging world. Help us make supply chains work better, faster, and be more resilient, with the following initiatives: Be a part of the Accenture Cost & Productivity Reinvention (C&PR) practice that has expertise in delivering projects with quantified savings in the indirect and direct categories. Support and lead Cost & Productivity Reinvention (C&PR) engagements, including sourcing for direct, indirect categories, conducting spend analyses, market intelligence, identifying cost reduction or process improvement opportunities, data analytics, so on. Take the lead on all digital sourcing and technology initiatives. Work towards Accentures Cost & Productivity Reinvention (C&PR) approach for EBITDA improvement including direct material cost transformation, indirect material cost transformation, logistics cost transformation, manufacturing efficiency improvement & cost transformation conduct data analytics across financial data and operational data. Deliver cost transformation engagements for clients across industries. Bring your best skills forward to excel in the role: Strong analytics skills driven by the next wave digital and technology initiatives Ability to solve complex business problems and deliver client delight Excellent communication, interpersonal and presentation skills Cross-cultural competence with an ability to thrive in a dynamic environment Read more about us. Recent Blogs Qualifications Your experience counts! MBA from Tier-1 B School 1-4 years of experience for an Analyst and 4-8 years of experience for a Consultant, across direct materials, manufacturing, logistics, market intelligence, EBITDA improvement programs , Business case development, Strategy formulation, Spend analysis across financial and operational data Experience in a consulting firm and global exposure is desirable. Retail, Healthcare, CG&S, Automotive, Industrial, Logistics industry experience would be preferred. Hands-on experience with analytical tools such as MS Excel, PowerBI, Alteryx would be an added advantage What’s in it for you? An opportunity to work on transformative projects with key G2000 clients Potential to Co-create with leaders in strategy, industry experts, enterprise function practitioners and, business intelligence professionals to shape and recommend innovative solutions that leverage emerging technologies. Ability to embed responsible business into everything—from how you service your clients to how you operate as a responsible professional. Personalized training modules to develop your strategy & consulting acumen to grow your skills, industry knowledge and capabilities Opportunity to thrive in a culture that is committed to accelerate equality for all. Engage in boundaryless collaboration across the entire organization. About Accenture: Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions — underpinned by the world’s largest delivery network — Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at www.accenture.com About Accenture Strategy & Consulting: Accenture Strategy shapes our clients’ future, combining deep business insight with the understanding of how technology will impact industry and business models. Our focus on issues such as digital disruption, redefining competitiveness, operating and business models as well as the workforce of the future helps our clients find future value and growth in a digital world. Today, digital is changing the way organizations engage with their employees, business partners, customers and communities. This is our unique differentiator. To bring this global perspective to our clients, Accenture Strategy's services include those provided by our Global Network – a distributed management consulting organization that provides management consulting and strategy expertise across the client lifecycle. Our Global Network teams complement our in-country teams to deliver cutting-edge expertise and measurable value to clients all around the world.For more information visit https://www.accenture.com/us-en/Careers/global-network At the heart of every great change is a great human. If you have ideas, ingenuity and a passion for making a difference, come and be a part of our team.