290 Spectrophotometer Jobs

We are a reputed organization based at Ahmedabad and having business of sales and services of Milk testing instruments Pan India. Please visit our website https://www.Indifoss.com/ for more details. We are hiring for the position - Sr. Sales Executive/Sales Executive Deputed Location (from where candidate will operate): Kolkata Territory offered to Handle: EAST Region Experience Required: 2 5 Years Qualification: Any Science Graduate with instrument sales experience Prospecting leads and contacting them to pitch in Dairy & Cattle Feed Industries Setting up meetings with the prospective clients Presenting product/ service demonstrations to the client Participate in conferences, exhibitions, and industry meetups for business development. Conduct market research to evaluate gaps, opportunities, and alien needs. Seek new opportunities through networking, cold calling, and social media channels. Organizing sales visits. Building and maintaining a CRM database and records. Attending trade exhibitions, conferences and meetings.

Our plant is in Sihor, Bhavnagar and we have a requirement of QC Chemist. If you are comfortable to shift to Sihor, Bhavnagar, do share your CV on khushbushah@jenburkt.com We are looking for candidates who have completed MSC. Overall: Fresher to 1 yr. of experience. CTC : Can be discussed on the call. Kind Regards, Khushbu

Company Description We at Mil laboratories are striving to make the goal of Health and Quality of life accessible to all. With the vision of making an impact on lives of healthcare professionals and their patients. Our initial success in Hospital Infection Prevention segment inspired us to scale new heights and venture into the Advanced Wound Care realm too. You will be responsible for the all quality control department related activity. J ob Title :- QC Incharge Job Description : Quality control executive Role Description · To perform all the testing related to RM, bulk, FP and stability samples · To perform all the testing of packaging materials · Handling of QMS documents like SOP, CAPA, repeat analysis, Deviation etc. · To manage and lead the team · To perform analytical method validation · To prepare specifications for different materials · New vendor approval · Should have working experience of HPLC, GC, UV spectrophotometer, centrifuge etc. What will you need to be successful? · Preferred experience in sterile pharma plant. · Extensive understanding of sterile and disinfectant products, GMP and GLP · Should have faced and experienced regulatory audits · Positive attitude, problem solving and time management · Should have a knowledge of ICH guidelines and other standards Experience – 4 to 5 years CTC – 4.5 to 5.0 LPA (based on experience & ability) Location – Mil Laboratories Pvt. Ltd. 541, GIDC, Manjusar, Ta. Savli, Dist. Vadodara - 391775 *FRESHER with MSc chemistry can also apply Interested and relevant applicants can send their profile to hr-pd@millaboratories.in or can watsup on 97648 42870

Key Responsibilities: · Lead and manage QC operations for raw materials, in-process, and finished products. · Oversee analytical testing methods: HPLC, UV Spectrophotometer, Kjeldahl, KF Titrator, SDS-PAGE, Hydroxyproline test, Protein content analysis. · Review and approve COAs, protocols, and reports in compliance with GMP, ISO 13485, and 21 CFR Part 11. · Ensure calibration and preventive maintenance of QC instruments. · Train and mentor QC team to maintain accuracy, compliance, and data integrity. · Handle deviations, OOS/OOT investigations, and implement CAPA. · Ensure audit readiness and regulatory compliance at all times. · Prepare, review, and control QC documents (SOPs, protocols, reports, records). · Approve test protocols and reports; ensure proper record keeping. · Plan and utilize manpower, equipment, and consumables effectively. · Oversee method validation, verification, and transfer for chemical and microbiological tests. Qualifications & Experience: · M.Sc. (Chemistry / Biochemistry) or B.Pharm / M.Pharm. · 5-8 years of QC experience in pharmaceuticals / medical devices / biotech, · Strong knowledge of analytical techniques and regulatory requirements. · Experience in handling customer and regulatory audits preferred. Job Type: Full-time Pay: From ₹35,000.00 per month Benefits: Paid sick time Paid time off Experience: hr: 2 years (Preferred) HR sourcing: 1 year (Required) Language: English (Required) Work Location: In person

Location: Hyderabad (Medchal) Handling Gravimetric / Instrumental analysis metals in samples, RND Support Key Responsibilities: Key Responsibilities: Testing of precious metal samples by gravimetric / fire assay test methods Ensuring test results through QC samples, repeatability, and reproducibility Daily calibration of analytical balances and maintaining records Maintaining best laboratory practices Maintaining good housekeeping and cleanliness in laboratory premises Key Authorities: Fire assay analysis Wet chemical testing Gravimetrical testing Internal calibration of lab instruments Testing of samples allotted by the Technical Manager Key Functional / Technical Competencies: Classical techniques and wet chemistry Fire assay analysis Calibration of basic lab instruments Health and safety guidelines

Job Summary: We are looking for a Sales Engineer with 3-6 years of experience in the pharma / life sciences industry , having a strong background in sales of analytical / laboratory instruments such as HPLC, HPTLC, GC, UV Spectrophotometer, Dissolution Tester, FTIR, ICP, TOC Analyzer . The ideal candidate will be responsible for lead generation, client acquisition, order closing, and achieving sales targets while handling technical and commercial discussions with customers. Key Responsibilities: Generate leads and follow up on opportunities in pharma / life sciences sector. Understand client requirements for analytical and laboratory instruments. Conduct technical discussions and product presentations with customers. Manage client meetings, negotiations, and order closing . Achieve monthly and quarterly sales targets and prepare sales projections. Build and maintain strong customer relationships across all levels (QC, QA, R&D, Purchase, Management). Track competitor products and market developments. Provide timely reporting, documentation, and sales communication. Travel across assigned territory (local + regional) for client visits. Qualifications: B.E / B.Tech in Electrical, Electronics (ECE/EIE), Instrumentation OR B.Sc / M.Sc in Microbiology Experience Required: 3-6 years of relevant experience in sales of pharma analytical instruments . Skills: Strong communication & presentation skills. Ability to convince customers with logic and technical clarity. Knowledge of analytical instruments (HPLC, GC, UV, Dissolution Tester, etc.). Target-oriented and self-motivated with a positive attitude. Good reporting and documentation skills. Working Conditions: Frequent travel by bus, train, or bike (within 100 km radius). Travel with calibration kits / demo instruments if required. Flexible to work late nights / weekends if client situations demand. Candidates Preferred: Pharma / Life Sciences Background ✅ Sales of Analytical & Scientific Instruments (HPLC, GC, UV, Dissolution, FTIR, ICP, etc.) ✅ 3-6 Years Sales Experience. Interested candidates can share resume at careers@shreedhargroup.com Job Types: Full-time, Permanent Pay: ₹42,000.00 - ₹75,000.00 per month Work Location: In person

Job Vacancy – Lab Analyst (Reputed Testing Laboratory Company) Location: Dhanbad Vacancy: 2 Timing: 10 AM – 6 PM Salary: ₹12,000 (with growth opportunities) Experience: Freshers & Experienced Both Qualification:- B.Sc / M.Sc in Biotechnology, Microbiology, Chemistry, Environmental Science, Food Technology, or related life sciences field. Skills Required:- Knowledge of laboratory testing methods & procedures Sample collection, preparation & analysis Data recording, documentation & report preparation Operating lab instruments (pH meter, spectrophotometer, etc.) Maintaining safety & quality standards in lab Job Role:- Conduct routine lab tests and experiments Analyze samples (chemical, biological, environmental, food & Water-based) Prepare accurate reports & maintain lab records Ensure compliance with lab protocols & safety norms Note: After 6 months, position will be permanent + salary hike & career growth in the company. Interested candidates DM with CV. 9296167856 Job Type: Full-time Pay: ₹11,000.00 - ₹12,000.00 per month Work Location: In person

1. Job Description: Manufacturing Chemist Company: Medicine manufacturer Location: Patiala, Punjab Role: Manufacturing Chemist Experience: 1 year Education: B.Sc./M.Sc. in Chemistry, Pharmacy, or a related field Package: ₹25,000 - ₹40,000 per month Shift: 9:00 AM - 6:00 PM Summary: We are seeking a dedicated and experienced Manufacturing Chemist to join our production team in Patiala. The ideal candidate will have hands-on experience in pharmaceutical manufacturing, a strong understanding of cGMP regulations, and a commitment to quality and safety. Key Responsibilities: Production Operations: Oversee and execute the manufacturing of pharmaceutical products according to Standard Operating Procedures (SOPs) and batch production records. Process Control: Monitor and control manufacturing processes to ensure product quality and consistency. Documentation: Maintain accurate and detailed records of all production activities, including equipment logs, batch records, and cleaning logs. Equipment Management: Operate, clean, and maintain manufacturing equipment to ensure optimal performance and compliance. Compliance: Adhere to all cGMP (current Good Manufacturing Practices) and safety protocols to ensure a safe and compliant working environment. 2. Job Description: Analytical Chemist Company: Medicine manufacturer Location: Patiala, Punjab Role: Analytical Chemist Experience: 1 year Education: B.Sc./M.Sc. in Chemistry, Pharmacy, or a related field Package: ₹25,000 - ₹40,000 per month Shift: 9:00 AM - 6:00 PM Summary: We are looking for a skilled Analytical Chemist with 1 year of experience in a pharmaceutical quality control lab. The successful candidate will be responsible for conducting chemical and physical tests on raw materials, in-process samples, and finished products to ensure they meet quality standards. Key Responsibilities: Sample Analysis: Perform a variety of analytical tests using instruments such as HPLC, GC, UV-Vis Spectrophotometer, and others. Method Validation: Assist in the validation and development of new analytical methods as required. Documentation: Accurately record all test results, observations, and calculations in laboratory notebooks and official documents. Equipment Maintenance: Calibrate and maintain laboratory equipment and instruments to ensure accuracy and reliability. Compliance: Ensure all testing procedures and documentation comply with cGMP, GLP (Good Laboratory Practices), and other regulatory guidelines. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Education: Master's (Preferred) Experience: Medicine Manufacturering: 1 year (Required) License/Certification: B.Sc/M.Sc (Required) Work Location: In person

Key Accountabilities And Responsibilities Analytical Method Development of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical Method Validation of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical Method Transfer of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. JOB SPECIFICATION Analytical method development and validation for pharmaceutical dosage forms. Literature search related to the drug substance, create analytical profiles. Execution of analytical method transfer for pharmaceutical dosage forms. Analysis of routine samples (product development batches, stability study samples, raw materials etc.). Operation and Calibration of analytical instruments/equipment’s. Qualification of working standards. Data Review and Release (as assigned). Documentation of analytical activities as per Good documentation practices. Work in laboratory as per Good laboratory practices. To use PPEs and follow safe practices in lab. Preparation of SOPs, STPs, Specifications, COAs and stability reports Preparation of RM Specification and STPs Trouble shooting of analytical issues/problems/queries. Review of Analytical development & stability data. Analytical Activities related to Quality Control Department. Any other task assigned by management. Competencies Required Good Knowledge about Analytical Method development, Validation and method transfer Knowledge about the Regulatory requirement and Quality requirement Must be able to perform the analysis as per the Good Laboratory Practices Functional Skills/ Know-how Hands on experience on HPLC, GC, UV spectrophotometer, IR spectroscopy, Dissolution Test Apparatus, Disintegration Test Apparatus, Viscometer, Differential Scanning Calorimetry (DSC), Malvern Particle sizer.

Academic Experience: University graduate or equivalent (in the specific area of competence: Chemistry /Microbiology ) Operational Experience: Demonstrated analytical background or laboratory exposure (performing analyses in the specific area of competence) Knowledge of ISO-17025 and Nestle Metod Validation/Verification guidelines Purpose: 1) Responsible for managing and organizing laboratory operations of respective section i.e all aspect of analytical related activities including TAT and budget preparation. 2) Executing the first line supervision of laboratory personnel to ensure the analytical works are professionally carried out, to ensure accuracy & reliability of analytical results. Responsible for cross checking and validating the analytical results for release to customer. 3) Developing and maintaining an effective laboratory workforce by constantly improving the work methods and analytical competence of subordinates. 4) Implement and maintain quality system according to the ISO /IEC17025 requirements and the Nestlé Quality System within NQAC Moga. Roles and Responsibilities Laboratory Management: Team Management, cascading of KPIs & goals Implement Safety regulations in the team to ensure a safe working environment for all. Awareness of team on safety zooms. Manage the activities of the team, report analytical results to factories/divisions in defined waiting time, ensure correct prioritisation and allocation of work. Hands on Experience on analytical methods of respective area Instrument troubleshooting, ensure the on time maintenance of equipments as per CMC/AMC plan. Manage Inventory and ensure chemical/consumable/Gas cylinders ordering on time. Ontime SES for timely payment. To assist Lab Manager to plan and liaise with factories/divisions concerning current and future work. Ensures appropriate and efficient use of NQAC resources (personnel, equipment,Capex and Sundry budget). In conjunction with Nestec,assist Lab Manager to identify and evaluate new techniques/methodologies to improve quality/performance of chemistry testing, taking full account of financial impact on the business. Technical knoweldge on different techniques (HPLC, LCMSMS,UPLC,Spectrophotometer), methods (specifically for Vitmians & Aflatoxins) and impact on results. Drive continous Improvement through implementation of NCE methdology. Investigation, root cause analysis and ensure corrective actions for complaints, non conformances, Questionable & Unsatisfactory results through GSTD and other NCE tools. Ensure timely and satisfactory response to all customer technical queries received. Manage analytical queries from stakeholders (e.g. Factories, comanufating units, CQA, regulatory etc) Ensure timely response to method relaled queries or requirement of comments on various analytical methods i.e. Nestle, official, draft methods by official bodies etc. Quality system: Establish validation files, MU calculation for new and exisiting methods according to Nestle validation standards and ensure accreditation to ISO17025 in accordance with business needs. Keep record of validation data. Ensure accreditation of new anlalytes and new matrices. Ensure documentation as per requirement of Management system. Ensure updation of relavant Managment procedures and formats Appropriate corrective action in the event of adverse analytical results. Ensure compliance to Good Laboratory Practice (GLP) policies in NQAC through regular internal/external auditing. To ensure Laboratory activities e.g. equipment maintenance Q-Stat and GLP etc are well executed by the team members. Drive continous improvement through internal/external verification (Audits) Responsible for the impartiality of its laboratory activities and is not influenced under commercial, financial or other pressures to compromise impartiality. Maintains Confidentiality of all information obtained or created during the performance of laboratory activities. Coach for GSTD Proficiency: Ensures NQAC chemistry section completes obligations for Proficiency testing against both Nestec and external requirements. Identify ILCs for different parameters. Ensuring accurate & ontime results: workload planning for ontime analysis reports, reviews and authorises the analytical results analysis of results including opinions, out of norm notificationsand ensures analytical method monitoring development, modification, verification and validation of methods. Updation of Method SOPs on time. maintain correct & ontime calibration & preventive maintenace of equipments. Updation of Equipment SOPs, ICPs and Management formats related to equipment. Maintenance & updation of Equipment softwares & lab activities related Softwares Responsible for conducting vertical method audit as per plan. LIMS System: Knowledge of SAP LIMS knowledge of QC codes, method codes, Downloading of analytical report Use of regional cockpit Operational knowledge & troubleshooting of LACES Result transfer from instruments, QC batches and their archival Preparation & Management of Consummable types and lots We are Nestlé, the largest food and beverage company. We are 308,000 employees strong driven by the purpose of enhancing the quality of life and contributing to a healthier future. Our values are rooted in respect: respect for ourselves, respect for others, respect for diversity and respect for our future. With more than CHF 91.4 billion sales in 2018, we have an expansive presence with 413 factories in more than 85 countries. We believe our people are our most important asset, so we'll offer you a dynamic inclusive international working environment with many opportunities across different businesses, functions and geographies, working with diverse teams and cultures. Want to learn more? Visit us at www.nestle.com.Nestlé is committed to the accessibility of its recruitment process. If you require an adaptation during the recruitment process, please talk to your recruiter so we can support you effectively. All information will be treated confidentially. Nestlé is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process.

Key Skills: • Gas Chromatography • HPLC • Karl Fisher • UV-Visible Spectrophotometer, Sampling Techniques • Digital Polari meter • Titrations • Wet analysis Knowledge considered as extra • PH, LOD, Specific gravity, Density . Calibration of instruments 2. Analysis of lab samples and pilot plant samples. 3. Documentation of all project of synthesis and pilot plant. 4. To maintain the all data of R&D lab and pilot plant projects the calibration of IC 5. Maintain the system of housekeeping and 5-s 6. Preparation of Standards Volumetric solutions and standard of volumetric 7. To maintain the monthly data of GC, LC and WET Analysis. 8. Daily maintain the gas cylinder records. 9. To preparation the Standard for GC, LC. and WET lab 10. Method development of R&D project

Academic Experience: - University graduate or equivalent (in the specific area of competence: Chemistry /Microbiology ) Operational Experience: - Demonstrated analytical background or laboratory exposure (performing analyses in the specific area of competence) - Knowledge of ISO-17025 and Nestle Metod Validation/Verification guidelines Purpose: 1) Responsible for managing and organizing laboratory operations of respective section i.e all aspect of analytical related activities including TAT and budget preparation. 2) Executing the first line supervision of laboratory personnel to ensure the analytical works are professionally carried out, to ensure accuracy & reliability of analytical results. Responsible for cross checking and validating the analytical results for release to customer. 3) Developing and maintaining an effective laboratory workforce by constantly improving the work methods and analytical competence of subordinates. 4) Implement and maintain quality system according to the ISO /IEC17025 requirements and the Nestl Quality System within NQAC Moga. Roles and Responsibilities Laboratory Management: -Team Management, cascading of KPIs & goals - Implement Safety regulations in the team to ensure a safe working environment for all. Awareness of team on safety zooms. - Manage the activities of the team, report analytical results to factories/divisions in defined waiting time, ensure correct prioritisation and allocation of work. -Hands on Experience on analytical methods of respective area -Instrument troubleshooting, ensure the on time maintenance of equipments as per CMC/AMC plan. -Manage Inventory and ensure chemical/consumable/Gas cylinders ordering on time. Ontime SES for timely payment. - To assist Lab Manager to plan and liaise with factories/divisions concerning current and future work. Ensures appropriate and efficient use of NQAC resources (personnel, equipment,Capex and Sundry budget). - In conjunction with Nestec,assist Lab Manager to identify and evaluate new techniques/methodologies to improve quality/performance of chemistry testing, taking full account of financial impact on the business. -Technical knoweldge on different techniques (HPLC, LCMSMS,UPLC,Spectrophotometer), methods (specifically for Vitmians & Aflatoxins) and impact on results. -Drive continous Improvement through implementation of NCE methdology. -Investigation, root cause analysis and ensure corrective actions for complaints, non conformances, Questionable & Unsatisfactory results through GSTD and other NCE tools. - Ensure timely and satisfactory response to all customer technical queries received. Manage analytical queries from stakeholders (e.g. Factories, comanufating units, CQA, regulatory etc) -Ensure timely response to method relaled queries or requirement of comments on various analytical methods i.e. Nestle, official, draft methods by official bodies etc. Quality system: - Establish validation files, MU calculation for new and existing methods according to Nestle validation standards and ensure accreditation to ISO17025 in accordance with business needs. Keep record of validation data. -Ensure accreditation of new anlalytes and new matrices. Ensure documentation as per requirement of Management system. -Ensure updation of relavant Managment procedures and formats - Appropriate corrective action in the event of adverse analytical results. - Ensure compliance to Good Laboratory Practice (GLP) policies in NQAC through regular internal/external auditing. -To ensure Laboratory activities e.g. equipment maintenance Q-Stat and GLP etc are well executed by the team members. -Drive continous improvement through internal/external verification (Audits) - Responsible for the impartiality of its laboratory activities and is not influenced under commercial, financial or other pressures to compromise impartiality. - Maintains Confidentiality of all information obtained or created during the performance of laboratory activities. - Coach for GSTD Proficiency: Ensures NQAC chemistry section completes obligations for Proficiency testing against both Nestec and external requirements. Identify ILCs for different parameters. Ensuring accurate & on time results: - workload planning for on time analysis. -reports, reviews and authorises the analytical results -analysis of results including opinions, out of norm notificationsand ensures analytical method monitoring -development, modification, verification and validation of methods. Updation of Method SOPs on time. -maintain correct & ontime calibration & preventive maintenace of equipments. Updation of Equipment SOPs, ICPs and Management formats related to equipment. - Maintenance & updating of Equipment softwares & lab activities related Softwares -Responsible for conducting vertical method audit as per plan. LIMS System: Knowledge of SAP LIMS knowledge of QC codes, method codes, Downloading of analytical report Use of regional cockpit Operational knowledge & troubleshooting of LACES Result transfer from instruments, QC batches and their archival Preparation & Management of Consumable types and lots We are Nestl, the largest food and beverage company. We are 308,000 employees strong driven by the purpose of enhancing the quality of life and contributing to a healthier future. Our values are rooted in respect: respect for ourselves, respect for others, respect for diversity and respect for our future. With more than CHF 91.4 billion sales in 2018, we have an expansive presence with 413 factories in more than 85 countries. We believe our people are our most important asset, so we'll offer you a dynamic inclusive international working environment with many opportunities across different businesses, functions and geographies, working with diverse teams and cultures. Want to learn more? Visit us at www.nestle.com.Nestl is committed to the accessibility of its recruitment process. If you require an adaptation during the recruitment process, please talk to your recruiter so we can support you effectively. All information will be treated confidentially. Nestl is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process.

Academic Experience: University graduate or equivalent (in the specific area of competence: Chemistry /Microbiology ) Operational Experience: Demonstrated analytical background or laboratory exposure (performing analyses in the specific area of competence) Knowledge of ISO-17025 and Nestle Metod Validation/Verification guidelines Purpose: Responsible for managing and organizing laboratory operations of respective section i.e all aspect of analytical related activities including TAT and budget preparation. Executing the first line supervision of laboratory personnel to ensure the analytical works are professionally carried out, to ensure accuracy & reliability of analytical results. Responsible for cross checking and validating the analytical results for release to customer. Developing and maintaining an effective laboratory workforce by constantly improving the work methods and analytical competence of subordinates. Implement and maintain quality system according to the ISO /IEC17025 requirements and the Nestlé Quality System within NQAC Moga. Roles And Responsibilities Laboratory Management: Team Management, cascading of KPIs & goals Implement Safety regulations in the team to ensure a safe working environment for all. Awareness of team on safety zooms. Manage the activities of the team, report analytical results to factories/divisions in defined waiting time, ensure correct prioritisation and allocation of work. Hands on Experience on analytical methods of respective area Instrument troubleshooting, ensure the on time maintenance of equipments as per CMC/AMC plan. Manage Inventory and ensure chemical/consumable/Gas cylinders ordering on time. Ontime SES for timely payment. To assist Lab Manager to plan and liaise with factories/divisions concerning current and future work. Ensures appropriate and efficient use of NQAC resources (personnel, equipment,Capex and Sundry budget). In conjunction with Nestec,assist Lab Manager to identify and evaluate new techniques/methodologies to improve quality/performance of chemistry testing, taking full account of financial impact on the business. Technical knoweldge on different techniques (HPLC, LCMSMS,UPLC,Spectrophotometer), methods (specifically for Vitmians & Aflatoxins) and impact on results. Drive continous Improvement through implementation of NCE methdology. Investigation, root cause analysis and ensure corrective actions for complaints, non conformances, Questionable & Unsatisfactory results through GSTD and other NCE tools. Ensure timely and satisfactory response to all customer technical queries received. Manage analytical queries from stakeholders (e.g. Factories, comanufating units, CQA, regulatory etc) Ensure timely response to method relaled queries or requirement of comments on various analytical methods i.e. Nestle, official, draft methods by official bodies etc. Quality system: Establish validation files, MU calculation for new and exisiting methods according to Nestle validation standards and ensure accreditation to ISO17025 in accordance with business needs. Keep record of validation data. Ensure accreditation of new anlalytes and new matrices. Ensure documentation as per requirement of Management system. Ensure updation of relavant Managment procedures and formats Appropriate corrective action in the event of adverse analytical results. Ensure compliance to Good Laboratory Practice (GLP) policies in NQAC through regular internal/external auditing. To ensure Laboratory activities e.g. equipment maintenance Q-Stat and GLP etc are well executed by the team members. Drive continous improvement through internal/external verification (Audits) Responsible for the impartiality of its laboratory activities and is not influenced under commercial, financial or other pressures to compromise impartiality. Maintains Confidentiality of all information obtained or created during the performance of laboratory activities. Coach for GSTD Proficiency: Ensures NQAC chemistry section completes obligations for Proficiency testing against both Nestec and external requirements. Identify ILCs for different parameters. Ensuring accurate & ontime results: workload planning for ontime analysis reports, reviews and authorises the analytical results analysis of results including opinions, out of norm notificationsand ensures analytical method monitoring development, modification, verification and validation of methods. Updation of Method SOPs on time. maintain correct & ontime calibration & preventive maintenace of equipments. Updation of Equipment SOPs, ICPs and Management formats related to equipment. Maintenance & updation of Equipment softwares & lab activities related Softwares Responsible for conducting vertical method audit as per plan. LIMS System: Knowledge of SAP LIMS knowledge of QC codes, method codes, Downloading of analytical report Use of regional cockpit Operational knowledge & troubleshooting of LACES Result transfer from instruments, QC batches and their archival Preparation & Management of Consummable types and lots We are Nestlé, the largest food and beverage company. We are 308,000 employees strong driven by the purpose of enhancing the quality of life and contributing to a healthier future. Our values are rooted in respect: respect for ourselves, respect for others, respect for diversity and respect for our future. With more than CHF 91.4 billion sales in 2018, we have an expansive presence with 413 factories in more than 85 countries. We believe our people are our most important asset, so we'll offer you a dynamic inclusive international working environment with many opportunities across different businesses, functions and geographies, working with diverse teams and cultures. Want to learn more? Visit us at www.nestle.com.Nestlé is committed to the accessibility of its recruitment process. If you require an adaptation during the recruitment process, please talk to your recruiter so we can support you effectively. All information will be treated confidentially. Nestlé is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process.

Location: Hyderabad Handling BET, XRD and XEM with a minimum of 4-10 years of experience. Key Responsibilities: Gravimetric / Instrumental analysis metals in samples, RND Support 2 Analysis using Instrumental Techniques like ICP, BET, Particle Size, Chemisorption, Hydrogen Uptake, XRF and HPLC 3 Record and Report Management 4 Following best practices in laboratory as per the directional support from Senior Staff. 5 Delivering and maintaining high quality and accurate results during handling and analyzing samples 6 Meet and/or exceed the Analytical Objectives and Goals 7 Execution of Calibration plan of Analytical Balances, Instruments and maintaining records 8 Implementing Health and Safety Guidelines 9 Working as Technical manager for NABL/ISO compliances Key authorities : 1 Method Development & Validation 2 Working on ICP-OES, BET, Particle Size Analyzer, Chemisorption, Hydrogen Uptake, XRF and HPLC 3 Analytical Troubleshooting 4 Internal Calibration of Lab Instruments 5 Implementing testing Plan for daily samples Documentation as per ISO 17025:2017

Role & responsibilities : QC - Biologics(Instrumentation, Activity / Potency based assays, Hematology, Biochemical group) Preferred candidate profile

Shift: 9:30 am to 5:30 pm (Sometimes rotational shift including night shift) Benefits: Food provided, Company bus pickup and drop Job Profile and Responsibilities To analyze in-process samples for Semi-Finished Goods & Raw Materials as per the Standard specification. To operate instruments like Spectrophotometer for shade analysis of Dye samples and absorbance of Material. Co-ordinate with export team for outgoing reference and pre-shipment samples. Documentation as per the ISO Norms Knowledge regarding Leather and Textile Dyeing Candidate Profile ITI/ Diploma- Chemicals Age- 20 to 25 Years age. Gender- MALE Experience- Freshers Notice Period- Immediate Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹17,000.00 per month Benefits: Commuter assistance Food provided Provident Fund Ability to commute/relocate: Taloja, Navi Mumbai, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Work Location: In person

Wet chemical analysis of food and water samples. Instrumental analysis of food samples on HPLC, UV-Vis spectrophotometer. Volumetric solution preparation and its standardization. Distillation for food analysis. Maintenance of lab records. Knowledge of ISO 17025:2005 standard.

Job Description: Role: DM Plant Incharge – Chemist Experience: 5–10 years in DM plant operations in thermal or biomass power plants, with at least 2 years in a supervisory/in-charge role. Location: Phalodi, Rajasthan Reports To: Plant Manager / Operations Manager Employment Type: Full-time Salary Range: 3.6 to 4.8 LPA Job Purpose: To manage and oversee the operation, maintenance, and quality assurance of the Demineralisation (DM) Water Treatment Plant in a Biomass Power Plant, ensuring uninterrupted and high-purity water supply for boiler and turbine operations, in full compliance with plant safety, operational efficiency, and environmental regulations. Key Responsibilities: 1. DM Plant Operation & Water Quality Management Operate and supervise the entire DM water treatment process, including RO (Reverse Osmosis), EDI (Electrodeionization), Softener, Degasser Tower, and Mixed Bed units. Ensure a consistent and reliable supply of DM water with required quality parameters (conductivity, silica, pH, total hardness, etc.) for high-pressure boilers and turbines. Conduct regular chemical analysis of raw water, DM water, condensate, and feedwater to maintain steam purity and avoid boiler/turbine scaling and corrosion. 2. Equipment Monitoring & Maintenance Ensure optimal performance and preventive maintenance of DM plant equipment, dosing systems, pumps, and control panels. Troubleshoot process issues like conductivity spikes, regeneration failures, or membrane fouling. Coordinate with maintenance and instrumentation teams for timely repairs and calibration. 3. Documentation & Compliance Maintain daily logs, chemical usage records, test reports, and regeneration schedules. Prepare reports for internal audits, environmental monitoring, and compliance with CPCB/SPCB norms. Ensure proper chemical storage and handling as per safety and MSDS guidelines. 4. Boiler Chemistry Interface Collaborate with boiler operations team to ensure feedwater and steam chemistry compliance (oxygen scavenger dosing, phosphate control, etc.). Monitor condensate polishing unit (CPU) performance and manage condensate quality. 5. Team Supervision & Safety Supervise a team of water treatment technicians/operators. Conduct training and toolbox talks on chemical handling, safe plant operation, and emergency response. Enforce use of PPEs and safety protocols during regeneration and chemical handling. Key Skills & Competencies: Expertise in DM water production and boiler feedwater treatment. Strong understanding of steam-water cycle chemistry in thermal/biomass power plants. Familiarity with laboratory instruments: pH meter, conductivity meter, spectrophotometer, silica analyzer, etc. Knowledge of boiler chemistry guidelines (e.g., ASME, OEM specifications). Leadership, documentation, and root cause analysis skills. Qualifications & Experience: Education: B.Sc. / M.Sc. in Chemistry, Industrial Chemistry, or Environmental Science Experience: 5–10 years in DM plant operations in thermal or biomass power plants, with at least 2 years in a supervisory/in-charge role. Preferred Industry Background: Thermal Power Plants, Biomass Power Plants, Captive Power Plants (CPP), or large-scale industrial utilities with high-pressure steam generation systems.

Job Title: Process Chemist At FMC, our employees are guided by our purpose: Innovation for Agriculture, Solutions for the Planet. We provide farmers innovative solutions that increase the productivity and resilience of their land. From our industry-leading pipeline to novel biologicals and precision technologies, we are passionate about the power of science to solve agriculture’s biggest challenges. For more than a century, FMC has successfully delivered some of the of the industry's most advanced, innovative solutions that protect farmers’ crops from destructive pests and disease, while also protecting the environment. We are committed to fulfilling our mission of discovering new herbicide, insecticide and fungicide active ingredients, product formulations and pioneering technologies that are consistently better for the planet. Position Summary This position is an excellent opportunity for an initiative-taking individual to utilize their knowledge and experience in research and process development. Based in the IIC Hyderabad. The Process Chemist is responsible for developing, optimizing, and scaling up chemical processes from laboratory to pilot and production scale for new molecules and existing products. The role involves ensuring that processes are safe, efficient, cost-effective, and environmentally sustainable, while meeting quality and regulatory requirements. Location: IND - IIC Hyderabad The Role Develop and improve chemical processes for making new and existing products. scale up processes from lab level to pilot and full production. Coordinate with teams like production, quality control, safety, and regulatory. Follow safety and environmental rules. Transfer lab-developed processes to manufacturing plants and help solve any issues. Draft clear reports, batch records, and standard operating procedures (SOPs). Use and maintain lab equipment like reactors, chillers, and Chemical processing equipment's. Perform complex chemical reactions, Chiral chemistry, multi-step synthesis like halogenation and pressure reactions. Analytical data monitoring for the reaction using tools like NMR, IR, LC-MS, HPLC, GC, and GC-MS. Identify and study impurities- purification, crystallization, and distillation methods. Understand and control key process parameters to ensure consistent quality. Solving production issues and improving efficiency at different Tolling sites. Onsite support at Toller site for troubleshooting production issues and ensuring consistency. The Candidate Master’s degree in organic chemistry. 8-12 years of experience in process development/ R&D and chemical manufacturing. Strong knowledge of organic synthesis and chemical engineering principles. Experience in scale-up and pilot plant operations is preferred. Knowledge of structural elucidation and interpretation by using analytical techniques such as NMR, IR, LC-MS, HPLC, GC and GC-MS. Knowledge about TLC, Rota vapor, EYELA small-scale synthesizer, EYELA small scale pressure reactor, Buchi 20L reactor, UV Visible spectrophotometer, KF titrator, Huber thermostats, Julabo chilling systems. Good documentation and report-writing skills. Ability to work both independently and in a team environment. Multistep organic synthesis and custom Synthesis of molecules from gram to kilogram scale. [Chlorination, Bromination and Pressure reaction] Synthetic route optimization/process stabilization, validation, and determination of critical process parameters. Identification of impurities, their characterization and crystallization techniques. Capable of technology transfer related to process from R&D to plant level toller site and trouble shooting. Ag, / Speciality fine chemical experience strongly preferred. Travel to different Tolling sites is required. If you're a motivated leader with a strong technical background and a passion for safety and efficiency, we encourage you to apply for this dynamic role and join our team. At FMC, diversity and inclusion are in our DNA. We are proud to be an Equal Opportunity Employer with a commitment to creating an inclusive workplace where all employees can thrive – regardless of race, gender, sex, pregnancy, gender identity and/or expression, sexual orientation, national origin or ancestry, citizenship status, color, age, religion or religious creed, physical or mental disability, medical condition, genetic information, marital status, military or veteran status, or any other basis protected by federal, state or local law. FMC complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, please contact our Talent Acquisition department.

Job Title: Process Chemist At FMC, our employees are guided by our purpose: Innovation for Agriculture, Solutions for the Planet. We provide farmers innovative solutions that increase the productivity and resilience of their land. From our industry-leading pipeline to novel biologicals and precision technologies, we are passionate about the power of science to solve agriculture’s biggest challenges. For more than a century, FMC has successfully delivered some of the of the industry's most advanced, innovative solutions that protect farmers’ crops from destructive pests and disease, while also protecting the environment. We are committed to fulfilling our mission of discovering new herbicide, insecticide and fungicide active ingredients, product formulations and pioneering technologies that are consistently better for the planet. Position Summary This position is an excellent opportunity for an initiative-taking individual to utilize their knowledge and experience in research and process development. Based in the IIC Hyderabad. The Process Chemist is responsible for developing, optimizing, and scaling up chemical processes from laboratory to pilot and production scale for new molecules and existing products. The role involves ensuring that processes are safe, efficient, cost-effective, and environmentally sustainable, while meeting quality and regulatory requirements. Location: IND - IIC Hyderabad The Role Develop and improve chemical processes for making new and existing products. Scale up processes from lab level to pilot and full production. Coordinate with teams like production, quality control, safety, and regulatory. Follow safety and environmental rules. Transfer lab-developed processes to manufacturing plants and help solve any issues. Draft clear reports, batch records, and standard operating procedures (SOPs). Use and maintain lab equipment like reactors, chillers, and Chemical processing equipment's. Perform complex chemical reactions, Chiral chemistry, multi-step synthesis like halogenation and pressure reactions. Analytical data monitoring for the reaction using tools like NMR, IR, LC-MS, HPLC, GC, and GC-MS. Identify and study impurities- purification, crystallization, and distillation methods. Understand and control key process parameters to ensure consistent quality. Solving production issues and improving efficiency at different Tolling sites. Onsite support at Toller site for troubleshooting production issues and ensuring consistency. The Candidate Master’s degree in organic chemistry. 8-12 years of experience in process development/ R&D and chemical manufacturing. Strong knowledge of organic synthesis and chemical engineering principles. Experience in scale-up and pilot plant operations is preferred. Knowledge of structural elucidation and interpretation by using analytical techniques such as NMR, IR, LC-MS, HPLC, GC and GC-MS. Knowledge about TLC, Rota vapor, EYELA small-scale synthesizer, EYELA small scale pressure reactor, Buchi 20L reactor, UV Visible spectrophotometer, KF titrator, Huber thermostats, Julabo chilling systems. Good documentation and report-writing skills. Ability to work both independently and in a team environment. Multistep organic synthesis and custom Synthesis of molecules from gram to kilogram scale. [Chlorination, Bromination and Pressure reaction] Synthetic route optimization/process stabilization, validation, and determination of critical process parameters. Identification of impurities, their characterization and crystallization techniques. Capable of technology transfer related to process from R&D to plant level toller site and trouble shooting. Agrochemical / Speciality fine chemical experience strongly preferred. Travel to different Tolling sites is required. If you're a motivated leader with a strong technical background and a passion for safety and efficiency, we encourage you to apply for this dynamic role and join our team. At FMC, diversity and inclusion are in our DNA. We are proud to be an Equal Opportunity Employer with a commitment to creating an inclusive workplace where all employees can thrive – regardless of race, gender, sex, pregnancy, gender identity and/or expression, sexual orientation, national origin or ancestry, citizenship status, color, age, religion or religious creed, physical or mental disability, medical condition, genetic information, marital status, military or veteran status, or any other basis protected by federal, state or local law. FMC complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, please contact our Talent Acquisition department.

Roles and Responsibilities Conduct quality control tests on pharmaceutical products using instruments such as HPLC, UV, spectrophotometer, etc. Ensure compliance with cGMP guidelines and regulatory requirements. Maintain accurate records of test results, batch records, and inventory management. Collaborate with cross-functional teams to resolve issues related to product quality and stability. Perform routine maintenance tasks for laboratory equipment to ensure optimal performance.

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Job Description We are seeking a highly motivated candidate to support our Research & Development projects on Nanotechnology for Sustainable Energy and Water Solutions. As a research assistant, your role involves: Synthesis and characterization of the advanced nano materials. Conducting, and optimizing to test, validate and improve the efficiency of the developed material. Utilization for the application of photocatalysis, sensing, and energy storage devices. Working with collaborators to achieve identified tasks. Qualification MTech/MSc in Chemical Engineering, Chemistry, Material Science, Nanotechnology or related field (from a reputable institution) Preferred Skills Proven experience in experimental investigations, including test setup, data acquisition, and analysis. Hands-on experience with Potentiostat, UV and PL spectrophotometer is highly desirable. Experience working on Tools like Origin, Chem Draw. Effective communication and teamwork abilities. How to Apply Interested candidates should submit their resume and a cover letter detailing their experience in experimental investigations, and any work related to photocatalysis and electrocatalysis projects to aayushi@vtindia.in, career@vtindia.in

Perform chemical, physical, and instrumental analyses of raw materials, in-process samples, and finished products. Prepare reagents, standard solutions, and samples for testing as per established protocols Operate, calibrate, and maintain laboratory.

Company Description Founded in 1997 under the leadership of Mr. Jaideep Savla, S&S Packaging has grown to become a premier Printing and Packaging Company in India. With over five decades of experience, our company delivers quality, innovative solutions with a focus on speed and reliability. We specialize in Offset Printing and Rotogravure Printing, serving diverse industries like pharmaceuticals, FMCG, tobacco, textiles, and more. Headquartered in Mumbai, we operate a state-of-the-art manufacturing unit in Silvassa. Role Description This is a full-time on-site role for an Ink Executive located in Silvassa. The Ink Executive will be responsible for preparation, shade matching, and management of inks for paper-based printing & packaging jobs. This role ensures consistency, quality, and availability of inks while minimizing wastage and controlling costs. The position requires strong documentation and reporting skills to track ink usage, stock, and efficiency in the production process. Key Responsibilities: A. Ink Preparation & Shade Matching – Gravure Production Formulate, mix, and supply inks as per job requirements for paper substrates on gravure machine. Carry out accurate shade matching using spectrophotometer, shade cards, and visual standards. Maintain ink viscosity and properties for optimal print results on paper. B. Production Support Ensure timely supply of inks to gravure printing machines to avoid downtime. Troubleshoot ink-related issues during production (e.g., foamng, smudging, drying). Adjust inks based on substrate absorption and finishing requirements. C. Reporting & Documentation Prepare and maintain reports including: Ink Wastage Report (per job / per shift). Ink Consumption Report (job-wise, daily, monthly). Stock Level Report (available, slow-moving, near expiry). Cost Monitoring Report (ink usage vs. job output). Maintain ink performance data for continuous improvement. Maintain a database of formulations, shade references, and approval records . Present periodic MIS reports to Production Manager. D. Inventory & Vendor Coordination Monitor ink stock levels and raise requisitions for replenishment. Coordinate with suppliers for technical support and shade approval trials. Ensure proper storage of inks, and coatings to avoid spoilage. Key Skills & Competencies: Strong knowledge of inks for paper-based substrates . Proficiency in shade matching, color measurement tools, and viscosity control . Experience in documentation, data entry, and MIS reporting. Analytical mindset to identify wastage trends and suggest cost-saving measures. Good coordination with production, QA, and purchase teams. Qualifications & Experience: Diploma / Degree in Printing Technology, Chemistry, or related field. 2–5 years of experience in Ink Kitchen / Ink Department in paper-based printing & packaging . Hands-on experience with color matching and ink inventory management is a must.