291 Spectrophotometer Jobs - Page 9

Role & responsibilities Physicochemical characterization, Media preparation, Buffer preparation etc. Preferred candidate profile Experience in working in lab set up and good basic knowledge on physical/chemical techniques. Dilligent and accuracy driven.

WE ARE HIRING R&D + QC OFFICER We are looking for one experienced candidate who can handle both Research & Development (R&D) and Quality Control (QC) responsibilities in our Herbal Extraction Unit. Requirements: Develop and optimize herbal extraction processes Conduct quality testing (raw materials & finished extracts) Maintain lab records & documentation Ensure GMP, safety, and compliance Good working knowledge of HPLC and UV spectrophotometer is essential Contact Us On :- Official@zivishaherbal.com

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt. Ltd.! We're hiring a Quality Control Head for our client. Qualification: MSc in Chemistry, Biochemistry, or a related field Location: Vikarabad District, Telangana Experience: 5 to 8 Years Salary: 3.5 lakhs to 4 lakhs per annum Required: Male Note: Preferably with strong experience in the pharmaceutical or ethanol industry. Job Summary: We are seeking an experienced Quality Control Head to lead the QC team at our client's facility. The ideal candidate will have a strong background in analytical techniques, including Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC), and will be responsible for ensuring the highest standards of product quality and regulatory compliance. Responsibilities: Lead, manage, and mentor the Quality Control team. Develop, implement, and oversee all QC procedures and protocols. Supervise analytical testing using GC, HPLC, Spectrophotometer, and other advanced techniques. Ensure all processes and products comply with regulatory requirements and industry standards (e.g., ISO, GMP). Collaborate effectively with production teams to identify and resolve any quality-related issues. Develop and implement robust quality control measures to guarantee final product quality. Train and develop QC team members to enhance their skills and performance. Requirements: Minimum of 5 to 8 years of experience in a Quality Control role. Strong hands-on knowledge of analytical techniques, especially Gas Chromatography (GC) and HPLC. Proven experience with regulatory compliance (e.g., ISO, GMP). Excellent leadership, communication, and problem-solving skills. Proactive, detail-oriented, and able to work in a dynamic environment. (Interested candidates can share their CV to aradhana@hungrybird.in or reach us at 9959417171.) Please furnish the below-mentioned details; that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: RAMESH, QC HEAD, 6 YEARS, 30 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards Aradhana +91 9959417171

To conduct and document analytical method validation (AMV), method verification, and method transfer activities for raw materials, in-process samples, and finished pharmaceutical products in compliance with ICH Q2(R1) , GMP , and regulatory standards . Key Responsibilities Analytical Method Validation Perform validation of analytical methods as per ICH Q2(R1) guidelines for: Assay and related substances (HPLC, UV) Dissolution, content uniformity, residual solvents (GC) Identification and other physicochemical parameters Conduct validation parameters: specificity, accuracy, precision, linearity, robustness, LOD/LOQ, system suitability, etc. Document results in validation protocols and summary reports. Method Verification Verify compendial methods (IP/BP/USP/Ph.Eur.) for RM/FP/IP samples. Confirm suitability of method for intended use before routine application. Prepare method verification reports and submit for review/approval. Method Transfer Participate in analytical method transfer (AMT) from R&D or third-party units. Execute comparative testing for transferred methods and compile transfer protocols. Coordinate with sending/receiving sites for method harmonization and troubleshooting. Instrument Handling Operate and troubleshoot instruments such as: HPLC (Empower, LabSolutions, Chromeleon) GC (Headspace, FID) UV-Visible Spectrophotometer FTIR, Dissolution Apparatus, TOC (if applicable) Documentation & Compliance Prepare and review: Validation protocols and reports Analytical worksheets and system suitability documents Adhere to GMP, GLP, and ALCOA+ principles. Maintain instrument logs, change controls, and CAPA logs where applicable. Audit Readiness & Regulatory Support Ensure all AMV data is audit-ready and compliant with regulatory expectations. Support in regulatory inspections (USFDA, MHRA, WHO-GMP, etc.). Address audit observations related to analytical validation. Instruments & Software Used HPLC, GC (Headspace, FID) UV-Vis Spectrophotometer, FTIR Dissolution Testers CDS Software: Empower / LabSolutions / Chromeleon Education :M.Sc. (Analytical / Organic Chemistry) / M.Pharm

Post for QC Chemist in Pharma Formulation Unit - based at Vatva, Ahmedabad, Gujarat. Sections - Tab, Cap, Syp, Cream, Mouthwash, Dry Powder, SoftGels Required Work Experience - Testing of Finished Formulation, API & Excipients Testing on Instruments like HPLC, Spectrophotometer, Dissolution Test Apparatus, Karl Fischer, Potentiometer, Titration, PH Meter, Analytical Balance, Hot Air Oven, etc. Work Experience - Required of QC Lab of Pharma Formulation Unit or FDA Approved Drug Testing Labs of Public or Private Sectors. Candidates (Do not apply for this job post) - with work experience from Other sectors like API, Dyes & Chemicals, Water Purification, Cosmetics, etc. Job Types: Full-time, Part-time Benefits: Flexible schedule Paid sick time Schedule: Day shift Supplemental Pay: Overtime pay Education: Bachelor's (Required) Experience: Quality control of Formulation Testing: 3 years (Preferred) Work Location: In person

We are seeking experienced chemists to join a talented and highly motivated team, involved in the purification of organic compound. The responsibilities will include pursuing a diverse R & D Program. Candidates should have an M. Sc. Degree in Organic Chemistry and have some working experience in HPLC and spectrophotometer.

Were Hiring: Service Engineer – TechnoValue Solutions Pvt Ltd Location: Navi-Mumbai / Hyderabad | Full-Time | Experience: 1–3 Years (Freshers with strong technical background can also apply) TechnoValue Solutions Pvt Ltd is looking for a dynamic and technically skilled Service Engineer to support our pharma clients with the installation, servicing, and maintenance of high-end laboratory and pharmaceutical instruments. Key Responsibilities: Installation, calibration, and servicing of pharma lab instruments at client locations Provide preventive maintenance and on-call technical support Troubleshoot and resolve issues related to hardware/software Maintain service records and submit reports regularly Ensure timely and professional support to pharma clients Requirements: Diploma/Degree in Electronics & Telecommunication, Instrumentation, Physics, Electronics Experience in handling pharmaceutical/laboratory instruments is preferred Good communication and problem-solving skills Willingness to travel to pharma plants, labs, and client locations Experience with HPLC, GC, UV-VIS, Dissolution Tester, or similar equipment will be a plus. Interested candidates can share their resume at technohr@technovalue.in or 8879773091. Join us in delivering reliable service and precision support to the pharma industry!

Company: Strides Pharma Science Limited Department: Quality Control Profile: Executive Locations: Bangalore Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry 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

Job Title : Analyst – Air/Water Location : Mohali Experience : 1 to 3 years Department : Environment Laboratory Employment Type : Full-Time Reporting To : Lab Incharge / Technical Manager About the Role : We are looking for an experienced and detail-oriented Analyst to join our Environment Laboratory team. The candidate must have prior experience in a NABL accredited lab with hands-on expertise in Air and Water analysis . Key Responsibilities : Conduct sampling and analysis of ambient air, stack emissions, drinking water, groundwater, and wastewater as per standard methods (e.g., APHA, BIS, CPCB guidelines). Operate and maintain laboratory instruments such as Spectrophotometer, BOD Incubator, COD Digester, pH Meter, and other relevant equipment. Ensure accuracy and reliability of test results with adherence to SOPs and quality protocols. Maintain proper documentation and records as per NABL ISO/IEC 17025 standards. Assist in calibration and validation of laboratory instruments. Follow safety practices and contribute to laboratory cleanliness and compliance. Coordinate with field staff for sample collection and support external audits/inspections. Desired Candidate Profile : B.Sc. / M.Sc. in Environmental Science, Chemistry, or related field 1–3 years of experience in Air/Water testing in a NABL accredited laboratory Familiarity with NABL documentation and audit requirements Proficiency in operating laboratory instruments Strong attention to detail and quality Good communication and teamwork skills Job Types: Full-time, Permanent Pay: ₹12,086.00 - ₹30,341.54 per month Schedule: Day shift Fixed shift Weekend availability Work Location: In person

Job Description 👇 1. Media preparation. 2. FSIP (Full Sterilization in process). 3. ESIP (Empty Sterilization in process). 4. Seed preparation. 5. Handling harvesting process. 6. Handling whole fermentation process (Monitoring/ observing fermenter during production batch). 7. Handling of autoclave for material preparation. Looking after autoclave setting & troubleshooting. 8. IPQC using microscope, spectrophotometer, pH meter. 9. Microscopy checks for all samples, seed, “0” hour media count. 10. Handling Centrifugation process/Operating. 11. Monitoring lyophilisation during lyophilisation cycle. 12. CP batch preparation. 13. Lyophilisation loading & unloading. 14. Filling TRF & sample handover to QC department for testing. 15. BMR filling. 16. DMRD media Blending & Preparation.

Job description :- Instrumental Analysis: Perform routine and stability analysis of raw materials, intermediates, and finished products using HPLC, UV-Vis Spectrophotometer, FTIR , etc. Operate and calibrate analytical instruments as per SOPs and regulatory guidelines. Troubleshoot HPLC and other lab equipment in coordination with service engineers when required. Documentation & Compliance: Prepare and maintain analytical reports, test data sheets, protocols, and logs as per GDP (Good Documentation Practices). Ensure all QC activities comply with cGMP, GLP, and other regulatory guidelines . Assist in investigation and documentation of OOS, OOT, and deviations . Sample Handling & Testing: Receive and analyze raw material, packaging material, in-process samples, and finished goods as per approved specifications. Maintain proper sample disposal records. SOP & Record Management: Review and update Standard Operating Procedures (SOPs), specifications, and analytical methods. Maintain laboratory notebooks, logbooks, equipment usage logs, and calibration records accurately. Equipment Handling & Calibration: Operate and maintain lab instruments including HPLC, Dissolution Test Apparatus, pH meter, Analytical Balance, etc. Conduct periodic calibration and qualification of instruments. Audit Readiness: Prepare and support internal and external audits (e.g., USFDA, WHO, MHRA). Maintain complete and audit-ready documentation at all times. Key Skills & Competencies: Hands-on experience in HPLC analysis and troubleshooting . Strong understanding of analytical chemistry, GMP, GLP , and ICH guidelines . Attention to detail, data integrity, and documentation accuracy. Good communication and team coordination skills. Proficiency in MS Office and LIMS (preferred). Qualifications: B.Pharm / M.Pharm / M.Sc / B.Sc (Chemistry or related field) Minimum 2–5 years of experience in QC in a regulated pharmaceutical environment . Additional Requirements: Willingness to work in shifts (if applicable). Sound knowledge of safety protocols and laboratory hygiene . Good analytical and problem-solving abilities. Familiarity with regulatory audits and compliance standards . Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Joining bonus Performance bonus Yearly bonus Work Location: In person Expected Start Date: 01/07/2025

Should able to perform and supervise following routine tests of general chemical nature:- To perform all tests on water i.e. pH, TDS, TSS, harnesses, alkalinity, BOD, COD etc. Pigment testing, Chemical Testing, application, analytical testing

Key Roles & responsibilities: A reputed Railway product manufacturer seek to hire an Operational Excellence Engineer within the Quality Assurance Team to participate in continuous improvement and efficiency projects, focusing on products, systems, operations and processes. Defines, designs, and implements process improvement as part of organizations Operational Excellence, supporting business in establishing "best practice". Responsible for the creating Quality assurance plans (QAPs) for Indian Railways, Inspection Test Plans (ITPs), Manufacturing Process Plans (MPP) Responsible for RDSO , RITES & Third Party inspection handling & documentations Responsible for the creating Quality documents (Both Export & Indian Market). Ensures integration and alignment both vertically and horizontally across organization, within areas of safety, quality, delivery, productivity, cost and process efficiency. Facilitate and coach improvement teams, establishes and maintain performance metrics to track program success. Lead in Lean health checks, apply Lean methodologies such as PDCA, and perform Lean program audits and streamlining processes. Implement standard work process/procedures, visual factory and error proofing mechanisms. Provide technical leadership on Operational Excellence/Lean systems and tools. Responsible for making SOPs and their implementations. Create, maintain and refine a Lean toolkit that can include 5S, Kaizen, quick change over, value stream mapping, mistake proofing and line balancing, Muda Walk, KANBAN, TEAMWOOD, SMED, POKA Yoke. Requirements: 1 to 3 years of exp. BE/BTech/Mtech in Mechanical/Industrial Engineering. Railways Industry experience with respect to inspection handling is preferred. Experience with Lean Manufacturing techniques, e.g. leading Kaizen events, Continuous improvement, Six Sigma, Process / Value stream mapping, FMEA, Fish Bone. Certified Six Sigma green belt will be preferred. Good understanding of industrial standards and risk management practices. Good technical capabilities, communication skills, teamwork abilities and initiative. Proficient in Microsoft Excel, Word, and PowerPoint

Company: Strides Pharma Science Limited Department: QA/QC Profile: Executive Locations: Alathur/Puducherry Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years

Jairamdass Khushiram have two herbal manufacturing units JK Botanicals Pvt. Ltd (Processing Unit) and SA Herbal Bioactives LLP (Extraction Unit),which are globally certified units with BRCGS , ISO, GMP, Kosher, Halal & Organic Certification Website - https://www.jairamdass.com/ Company Video :- https://youtu.be/SnDkfko3Cgs Qualification - BSc/B.Tech/ MSc in Lifesciences/ Botany/ Biotechnology/ Food Technology/Microbiology/ Chemistry Job location - Plot No. – M 14, Taloja MIDC Industrial Area Dist. – Raigad, Maharashtra 410208, Tondare Phata stop Post - QC Executive Job Profile :- Analytical Testing & Analysis: RM Analysis report. In-Process product analysis Reports Preparation reports for RM & FG Chemicals inventory management of Hot lab & Wet Lab HPLC UV spectrophotometer Colorimeter TLC Also have a knowledge of wet lab analysis like titrations, extractions, layer separations, gravimetric analysis, etc If interested please share your updated resume on hr@jairamdass.com Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Work Location: In person

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 Show more Show less

Key Responsibilities:Conduct physical and chemical testing of raw oil, refined oil, and final tray oil products. Perform routine analysis such as viscosity, density, acid value, moisture content, FFA (Free Fatty Acids), and other parameters. Calibrate and operate lab instruments such as GC (Gas Chromatograph), pH meter, Karl Fischer, Spectrophotometer, etc. Maintain proper documentation of test results and report deviations to the Quality Manager. Collect and retain production samples as per standard operating procedures (SOPs). Ensure all lab work complies with ISO, FSSAI, BIS, or other applicable standards. Maintain cleanliness and safety of lab equipment and environment. Assist in validation, shelf-life studies, and R&D trials for new oil formulations. Communicate with the production team to suggest corrections or improvements in process quality. Conduct inspections of packaging materials like tray seals, oils filled, and batch labelling. Participate in audits, internal reviews, and continual improvement activities.

• Knowledge of acid-base titration, sulphonation reaction testing, active matter content. • ability to operate standard lab instruments, pH meter, handling wet lab procedures • willing to learn: GC, HPLC, spectrophotometer, viscometer, etc.

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 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 Show more Show less

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 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: 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 Title: Textile Application Specialist (Manager/Sr. Manager) Location: Chennai Department: Textile Application Lab Reports To: Head – R&D/QC/NPD Type: Contract Job Summary: Seeking a Textile Application Specialist to support formulation testing and development. The role includes lab trials, data reporting, and coordination with R&D and marketing teams. Key Responsibilities: Conduct textile processing trials (Scouring, Bleaching, Soaping, Dyeing, Printing, Finishing). Operate lab instruments (HPLC, spectrophotometer, pH meter, etc.). Perform titrations, standard solution prep, and calibration. Collaborate with marketing on troubleshooting experiments. Maintain test records and prepare summary reports. Thorough knowledge of pulp and processing lab equipment. Qualifications: BE/B.Tech or Diploma in Textile Chemistry / Fashion Technology. 7+ years’ experience or fresher from a reputed textile institute. Strong knowledge of textile chemicals and lab procedures. Good communication, documentation, and teamwork skills. Show more Show less

Tips: Provide a summary of the role, what success in the position looks like, and how this role fits into the organization overall. Responsibilities Perform a part of Research in Anaerobic microbial cultivation documentation and data analysis Antimicrobial activity for a specific compound against the given microbes and documentation of the same Qualifications UG or PG Students who are studying currently and know the basic microbiological technique like serial dilution, plating, antimicrobial activities and UV spectrophotometer No. of Post 2 Period of internship 1 month (June 17, 2025- July 15, 2025) Stipend Rs. 3000/- Location K.S.Rangasamy College of Technology, Tiruchengode Certification DPIIT recognized Company certification Show more Show less

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 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: 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

Beckman Coulter Life Sciences’ mission is to empower those seeking answers to life’s most important scientific and healthcare questions. With a legacy spanning 80+ years, we have long been a trusted partner to our customers, who are working to transform science and healthcare with the next groundbreaking discovery. As part of our team of more than 2,900 associates across 130 countries, you’ll help drive our vision of accelerating answers—and our commitment to excellence. Beckman Coulter Life Sciences is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. This role will be an On-site role at our Beckman Coulter Life Science, Bangalore Development Center (BDC) manufacturing facility located in Bengaluru. Do you want to work in the Manufacturing Operations Team? Do you enjoy working in a dynamic work force, collaborating with other team members and diverse groups, to meet Organization goal and customer demand? Then read on! We are currently seeking a "Polymer Chemist 2" position in Production Operations who will be primarily responsible for polymer dye synthesis and related manufacturing processes. The company is compliant with ISO 9001: 2015, ISO 13485: 2016 & EN ISO 13485: 2016, MDSAP and Beckman Coulter corporate Quality system requirements. In this role, you will be responsible for: Experience in handing metal catalyst reactions. Experience in performing and optimization of C-N and C-C coupling reactions. Experience in handling air/moisture sensitive reagents and performing of reactions at the temperature range of -78ºC to higher temperatures. Perform purification of the organic compounds using different types of column chromatography techniques and other separation techniques. Having polymer chemistry and Conjugation chemistry knowledge with good Hands-on experience on HPLC/UPLC/GPC/TFF/Spectrophotometer/Fluorimeter and Automated purification system. The required qualifications for the job include: M.Sc. in Chemistry/Organic Chemistry/Polymer chemistry/Biochemistry or related discipline, with minimum of 5+ year’s industrial experience. Demonstrated ability to be flexible and resourceful. Ability to work in a team environment & Excellent communication skill. Previous experience with polymer chemistry and protein conjugation will have an added advantage. It would be a plus if you also possess previous experience in: Organic synthesis of fluorescent dyes suitable for Flow Cytometry applications. This job is eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical insurance to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

Location: Kurali, Karjan, Vadodara Qualification: B.Sc or M.Sc. Chemistry (Analytical chemistry/Inorganic chemistry) or Bachelor's in Food Technology or Food Science or Certified Food analyst by FSSAI. Experience: Should have 1 to 2 Years’ Experience in Analysis of Food from reputed Lab or Food industry. Experience in Analysis of Spices & related products may prefer. Reporting To: Manager Quality Area of Operations: Quality (QA/QC) Key Responsibilities 1. To Analyse and Manage overall Laboratory Testing & related Compliances. 2. To Manage the Samples of Raw materials, Packaging Materials, Semi finished, Finished Goods & R&D Which Provided for Testing. and Provide Results on time and Co Ordinate with the team for acceptance or rejection/On time Clearance. 3. To maintained all the Documentation related to Analysis & Laboratory. Must be Maintained the Stock of all the Laboratory Items and their Consumption on time with records. 4. To Store all the Retention & Controlled Samples as per the requirements and Maintain their records. 5. Responsible to do in house Calibration, Verification & Validation of Laboratory Items with proper Documentation as per the Std. Requirement. Should be able to coordinate for preventive maintenance for lab instruments. 6. Responsible to Maintain and Implementation of GHP, GLP, 5S and other Good Practices/Presentations in Laboratory. Should have knowledge of Good Laboratory Practices, NABL standard & FSSAI standards. 7. Responsible to Intimate any purchase or out of stock Lab. Items before 1 or 1.5 Month to the Reporting Manager wisely. 8. To maintain all the External lab. Test Reports and making of Certificate of Analysis on time. And Intimate before due date to next External test required. 9. Should be able to do Standardization of Prepared Chemicals to Check their Efficiency & Record keeping. 10. Able to Provide the basic Food safety/Chemical safety related Trainings to the Work Force. As & When Required. 11. Responsible to take care of all Glasswares, Instruments & Chemicals in Lab. To Avoid any Wastage/Breakage and has to be Maintained all time Safe Work Place in Laboratory. 12. Required hand on Experience to operate Moisture analyser, Hot air oven, Soxhlet apparatus, pH Meter, Titration, Centrifuge, Muffle furnace, BD meter, Sieve shaker, UV-Vis Spectrophotometer, Incubator, LAF, Autoclave, weigh balance, Dessicator, Mixture etc. 13. Should have good Computer skills (able to work on ERP system as & when required), Good Analytical skills with Accuracy. 14. Daily Reporting to the Quality Manager. Follow the Instructions form Reporting Manager and play supportive roll. Must be followed the Company's Rules and Regulations. Flexible to work in rotational shift. Ready to adopt any task/work from superior as & when required. Job Types: Full-time, Permanent Pay: ₹240,000.00 - ₹300,000.00 per year Education: Bachelor's (Preferred) Work Location: In person