36 Uv Spectrophotometer Jobs

Responsibilities: To conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods or stability samples. To calibrate, validate, or maintain laboratory equipment. To compile laboratory test data and perform appropriate analyses. He should able to handle Quality Control related Instruments like HPLC, GC, UV spectrophotometer, autotitrator, Karl Fischer, etc. To complete documentation needed to support testing procedures including data capture forms, equipment logbooks / inventory forms. To interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for releas...

Role Overview: As a member of the synthetic team, your primary responsibility will be to provide routine analytical support. This will involve monitoring reactions using HPLC/GC, analyzing intermediates and API. Additionally, you will be required to perform wet analysis tasks such as LOD, IR, Residue on Ignition, KF determination, and Titrations. Calibration of instruments like UV, IR, HPLC, GC, Autotitrator, and polarimeter will also be part of your duties. Writing LNB and ensuring all documentation is in compliance with 21 CFR regulations will be crucial. Furthermore, you will be responsible for preparing necessary documents for PDR. Key Responsibilities: - Provide routine analytical suppo...

Job Description: As the incumbent at Piramal Consumer Healthcare in the R&D department located in Rabale, Navi Mumbai, you will be responsible for handling and calibration of instruments. You should actively participate in routine analysis, instrumental analysis, stability study testing, and recording and maintaining lab data. Key Responsibilities: - Handle and calibrate instruments - Actively involved in routine analysis, instrumental analysis, stability study testing, and recording and maintaining lab data Qualifications Required: - 6 to 12 months of experience in the Pharma or chemical industry - Hands-on experience with analytical instruments like Viscometer, UV spectrophotometer, HPLC (...

Position: Junior Officer / Chemist Quality Control (QC) Industry: Pharmaceutical – API Manufacturing Location: Ankleshwar, Gujarat Department: Quality Control Experience: Minimum 2 Years (Pharma – API Experience Mandatory) No. of Positions: 2 Job Description: We are seeking a detail-oriented and experienced Junior Officer / Chemist – QC to support our API manufacturing unit's Quality Control operations. Key Responsibilities: Perform and monitor all QC activities including analysis of Raw Materials (RM) , Intermediates , and Finished Products Operate and calibrate laboratory instruments such as: HPLC GC UV Spectrophotometer FTIR Karl Fischer Titrator pH Meter Conductivity Meter Auto Titrator ...

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 deve...

Job Description: You will be responsible for delivering lectures, practical classes, and tutorials in Pharmaceutical Chemistry / Cognosy to undergraduate and postgraduate students. Additionally, you will design and implement curriculum updates in line with current industry trends and regulatory standards. Supervising student projects, dissertations, and lab research work will be a key responsibility. You are expected to guide students in the use of analytical tools and drug design software. Furthermore, initiating and publishing research in recognized national and international journals is an essential aspect of the role. Ensuring adherence to PCI, AICTE, and NAAC documentation and academic ...

Your Role: As part of our QC team, you'll focus on testing raw materials, in-process samples, and finished products to ensure they meet established specifications. Your job is to detect and prevent defects before products reach the market. Key Responsibilities: Conduct physical and chemical testing of raw materials and final products (pH, viscosity, stability, active ingredient analysis). Perform stability studies to ensure product consistency over its shelf life. Test emulsions, creams, lotions, gels, ointments, and serums for quality parameters like texture, fragrance, absorption, and spreadability. Verify the quality of packaging materials (bottles, tubes, jars, labels) to prevent contami...

Responsibilities: * Develop analytical methods, validate results. * Ensure compliance with GMP & WHO standards. * Conduct quality testing using HPLC & UV-VIS. * Manage QC processes, analyze data, report findings.

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Responsible to develop, implement and be responsible for the production plan for their respective departments. To deliver timely and accurate analysis of samples to meet customer commitments. Be responsible for re...

As a Scientist in this role, your primary responsibilities will include: - Executing experiments for analytical method development, qualification, and transfer - Conducting in-process and stability sample testing, biosimilarity analysis, and new high throughput formats of testing using chromatography (HPLC/UPLC), electrophoresis/capillary electrophoresis, UV spectrophotometer, Solo-VPE, and other high-end analytical tools - Analyzing samples in GC, Atomic absorption spectroscopy (AAS), Charged Aerosol Detector (CAD), and glycan analysis - Planning experiments sequentially and logically - Accurately recording experiment details in electronic laboratory notebook following good documentation pr...

We are seeking a highly skilled and motivated Senior Research Associate to lead and manage end-to-end research projects in our laboratory. The role requires strong technical expertise, hands-on experience with advanced instruments.

Job Description Handling of Potentiometer titration, Karl-Fisher , Calibration of Potentiometer titration , Karl Fischer , Handling of Polarimeter, Handling of UV Spectrophotometer, Handling & Calibration of PH meter, Show more Show less

Role & responsibilities Planning and Carrying out trials as per guidance and instructions of seniors. Tracking environmental microorganism development. Growing microbe cultures. Recording, analyzing and interpreting data. Perform laboratory analysis on all materials after appropriate sterilization. Perform tests on component samples, identify any contamination, conduct an analysis and initiate corrective measures. Study various cultures of microorganisms in isolation according to standard. Develop various testing processes for all new raw materials, finish product. Handling of basic instruments such as UV Spectrophotometer, pH meter, moisture balance etc. Media Preparation and fair knowledge...

Job Opportunity at Natco Pharma Limited (Formulation Unit) Department: Quality Control Position: Chemist / Officer / Executive Qualification: B. Pharmacy / M. Pharmacy / M. Sc Experience: 3 to 5 Years Location: Kothur, Telangana Key Responsibilities: Analysis of finished products, raw materials, and in-process samples Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus Testing of Packing Materials Adherence to GLP, GDP, cGMP, and ALCOA+ standards Assay and dissolution testing using HPLC Regulatory exposure in formulation is mandatory Interested candidates may share their CVs at jaganmohan.p@natcopharma.co.in

You will be joining the VTC MFG. QC Department as a Probationer-HO Staff, with a primary responsibility of ensuring the quality control of manufacturing processes. The ideal candidate should hold a M.Sc. degree in Biotechnology, Biochemistry, or Microbiology and have at least 3-7 years of hands-on experience in a relevant field, preferably with a background in the pharmaceutical industry. Your role will involve conducting various analytical tests and procedures such as RP-HPLC, SEC-HPLC/SE-HPLC, Dionex, IC/Ion Chromatography, Biochemical analysis, UV spectrophotometer, Protein, O-acetyl. It is essential to have a good understanding of these techniques and equipment to perform accurate qualit...

Role & responsibilities Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Analysis of raw material / finished products / stability samples / Dissolution profiling for R&D/ Plant support. Analytical Method Development /Verification Assay, Related substances, Dissolution etc . Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hot Air Oven, Refrigerator temperature monitoring. Develop/ optimize the analytical methods by Chemical/ instrument analysis Verify/ validate the analytical methods by Chemical/ instrument analysis Preparation / Revision of Specification and Method of analysis for Ra...

As an Analytical Chemist at our leading Contract Research Organization (CRO), you will have the opportunity to assist in conducting analytical testing of samples using instruments such as HPLC, GC, LC-MS/MS, and UV Spectrophotometer under supervision. You will play a crucial role in preparing reagents, solutions, and standards following Standard Operating Procedures (SOPs) with precision and attention to detail. Your responsibility will include accurately recording and maintaining raw data, logs, and reports in compliance with GLP/GMP standards. By ensuring proper documentation, you will play a pivotal role in meeting regulatory and internal audit requirements. You will provide essential sup...

Job Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Role Description: Quality control executive Location: Mil Laboratories Pvt. Ltd. 541, GIDC, Manjusar, Ta. Savli, Dist. Vadodara - 391775 Experience: 5 to 6 years Roles Responsibilities:- 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 unde...

You will be responsible for providing routine analytical support to the synthetic team for reaction monitoring by HPLC/GC and analysis of intermediates and API. In this role, you will perform wet analysis including LOD, IR, Residue on Ignition, KF determination, and Titrations. Additionally, you will be involved in the calibration of instruments such as UV, IR, HPLC, GC, Autotitrator, polarimeter, etc. Ensuring compliance with 21 CFR requirements, you will also be responsible for LNB writing and all related documentation. Furthermore, you will prepare the necessary documents for PDR. To excel in this role, you should possess good communication skills and be an effective team player capable o...

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Responsible to develop, implement and be responsible for the production plan for their respective departments. To deliver timely and accurate analysis of samples to meet customer commitments. Be responsible for re...

Position Overview We are seeking a dedicated and skilled Organic Chemist to join our dynamic team in Jaipur. This full-time position offers an exciting opportunity to contribute to innovative projects in the field of organic chemistry. The ideal candidate will possess a strong foundation in organic chemistry principles and methodologies, along with practical experience in quality assurance and testing. If you are passionate about advancing your career in a collaborative environment, we encourage you to apply. Key Responsibilities Conduct research and experiments in organic chemistry to develop new products and processes. Perform quality assurance (QA) analysis and testing to ensure complianc...

Job Description Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. Having analytical knowledge of Nasal/Derma products. 3. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 4. Ensuring data integrity policy, GDP and its effectiveness up to compliance 5. To maintain the stability chamber and tracker. 6. To maintain the stability chamber and tracker. 7. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience...

Role & responsibilities Responsible for analysis and documentation of in-process, finished products and stability samples. Handling of QMS, Preparations of Protocols and analytical documents. Preferred candidate profile Biological (Therapeutical Protein) sample Plate based analysis such as ELISA techniques (HCP, HCD, Protein A leachates), PCR, RT-PCR and SDS-PAGE methods. Bioassay analysis for finished products and stability samples by using Gen5 and PLA software. Maintenance of cell lines, Cell culture media and Revival of cell lines. Responsible for analysis of in-process, finished products and stability samples. Preparation of certificate of analysis. Preparation of standard operating pro...

Role & responsibilities Analysis of Routine and Stability samples using instruments like HPLC , UHPLC (Shimadzu), GC.UV spectrophotometer, IR, KF titrator and Dissolution tester. Having Experience in handling of Instruments, Like Analytical Balance, pH meter, KF Titrator, UV spectrophotometer, HPLC, UHPLC, Dissolution tester, GC is preferable Perform Calibration of instruments or equipment Like HPLC, Dissolution. Understanding of wet chemical analysis like: Titration, LOD, KF , IR, UV etc. Maintain analytical documentation records and online documentation of experiments. Understanding of analytical method development Activity. Execute routine Analytical research activities of drug products F...