152 Hplc Analysis Jobs

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: QC Quality Control Experience: (01- 07 Years) •HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC/ Micro-biology ARD - OSD Experience: (02-06 Years) •HPLC/ FG/Analytical Method validation/ Stability PACKING Experience: (01-06Years) •Blister Packing, Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) PRODUCTION Experience: (01-06Years) •Compression, Granulation, Coating, QUALIFICATION : ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B. Pharm, M.Pharm with relevant experience DESIGNATIONS: Operator, Jr. Officer, Officer & Jr. Executive NOTE: Offering a Joining bonus only for QC Depart. for Immediate Joiners Instrument experience in HPLC / G...

Having operating and technical knowledge of HPLC, GC, Ph meter, FTIR, Stability Study, IR and UV Knowledge of Process validation, cleaning validation and Calibration., Having of cGMP documentation & QMS SAP Analytical Method Validation for HPLC.

involve testing raw materials, in-process samples, and finished APIs for purity, strength, and quality using analytical instruments (HPLC, GC, etc.), ensuring strict adherence to GMP/GLP, maintaining detailed records, investigating deviations

Role & responsibilities Job Summary: We are seeking a detail-oriented and experienced Analytical R&D Chemist to join our synthesis lab. The ideal candidate will be responsible for developing, validating, and implementing analytical methods to support the research and development of new chemical entities and active pharmaceutical ingredients (APIs). This role requires a deep understanding of analytical chemistry, instrumental analysis, and method development. The Analytical R&D Chemist will collaborate with cross-functional teams to ensure the accuracy and reliability of analytical data. Key Responsibilities: Method Development and Validation: Develop and validate robust analytical methods fo...

We require "LAB TECHNICIAN for our client based at MUNDRA, GUJARAT. The said job opening is on contract basis which will be for a period of ONE YEAR and extended further depends upon client's requirement. Qualification & Experience : B. Sc in Chemistry /M.Sc chemistry with 3 + Yrs Experience in Instrument like GC ,HPLC and Sampling & Analysis of oil & product. Duty Hours : 8 Hours per day, Shift wise duty (Six days week) Accommodation managed by the candidates. Free Local Transportation. Food at site but subsidiary Rs. 30 /- Per days. If interested , please give your written confirmation for said terms & condition by reply mail, also request you to send your updated resume varsha@aarviencon....

Department - Quality Control (Shift Duty) Section - HPLC Experience - 2 to 6 years Qualification - M.Sc chemistry (Full time) Job description To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. To perform Analysis (Chemical)of raw material/packaging material/in-process samples /intermediate /bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample, PD lab sample etc. To ensure that all tests carried out in the laboratory are documented contemporaneously in an appropriate authorized and controlled worksheet/ bound book. To make entries in the sample in...

As a member of the team at Apotex Inc., you will be responsible for executing analytical method optimization, development, validation, and verification of various analytical test methods. Your role will involve working with Compendia, in-house developed methods, site transfer methods, regulatory queries, Method Life Cycle Management (MLCM) studies, Supplier Driven Changes (SDC), and other procedural updates. You will also be involved in the preparation of method validation/verification protocols and reports. Your key responsibilities will include: - Executing method optimization and development studies - Conducting method validation and verification of in-house methods, Compendia, SDC, MLCM,...

Job Description Of Q C chemist Qualification : B. Sc or M.sc in Chemistry Preferably in analytical chemist Description: Must have knowledge of computers & willing to work in shifts. Overall operation, calibration and troubleshooting as per GMP & SOP guidelines. Must have hands on experience in handling instruments like HPLC, GC, UV, ICP-MS, IR, KF titration, Wet Lab and chemical analysis of Raw Materials, Intermediate & finished products. Preparing document like method validation protocols and reports, specification and MOA for Finished product / Raw Material. Should have knowledge of Validation of APIs. Must know about the analysis of raw material and should handle the advanced analytical i...

As a member of the team, you will be responsible for: - Conducting HPLC analysis of Solid Orals and Nasal products - Hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products - Ensuring compliance with GMP/GLP practices Qualifications required for this role: - Bachelor's or Master's degree in Pharmacy or Science - 3-8 years of relevant experience - Immediate joiners are preferred Additional details of the company: You will have the opportunity to work in a fully automated, world-class manufacturing facility. You will be involved in working with diverse dosage forms in a multi-product environment. Additionally, you will receive attr...

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

Role & responsibilities Responsible for analysis and documentation of in-process, raw materials, finished products and stability samples. Handling of QMS, Preparations of Protocols and analytical documents Preferred candidate profile Biological (Therapeutical Protein) sample analysis by HPLC, UV, pH meter, Osmometer, ELISA and SDS-PAGE methods. Calibration of instruments and equipment as per the SOP. Responsible for analysis of in-process, finished products and stability samples. Raw material sampling and outsourcing activity. Preparation of certificate of analysis. Preparation of standard operating procedures, specifications, Protocols and standard testing procedures Operation of High Perfo...

Role & responsibilities Responsible for sampling and Instrumental/chemical analysis of RM, In-Process, Intermediate, Finished product, Cleaning samples, Validation samples, Market samples and Stability samples. Responsible to perform the calibration of instrument/equipment available in Quality Control laboratory. Maintain the laboratory as per GLP and GMP System. Sampling, Analysis, and review of raw material/packing material, Wet analysis i.e., water content, IR, UV, LOD, Assay by potentiometry, Sulphated ash etc, finished goods sampling, working on HPLC & GC instrument.

Urgent requirement For Food analyst -Testing Lab - Hyderabad , Shameerpet. Designation : Junior Analyst / Analyst / Senior Analyst Qualification : MSc (Chemistry /Analytical Chemistry) Industry : Food analytical Testing Lab Company : Vimta Labs Ltd Location : Hyderabad , Shameerpet Experience : 2- 10Years Primary Responsibilities: 1. To analyze all Food & Agri samples using HPLC as per IS, AOAC, FSSAI , SOP and customer supplied methods. 2. To Calibrate and perform Intermediate checks for all major and minor laboratory instruments such as HPLC, pH meter, micropipette, sonicator etc. 3. To analyze all the food & Agri samples using GC and UV-Visible spectrophotometer as per IS, AOAC, FSSAI and...

Perform sampling, testing, and analysis of raw materials, in-process materials, and finished products. Conduct analysis using analytical instruments such as HPLC, GC, UV, FTIR, pH meter, etc. Ensure all analytical activities comply with cGMP , GLP , and internal SOPs. Maintain accurate documentation, analytical reports, and laboratory records. Support method validation, calibration, and troubleshooting of analytical instruments. Ensure proper storage, handling, and disposal of chemicals and reagents. Assist in stability studies and routine quality checks. Coordinate with production, QA, and R&D teams for process improvements and issue resolution.

Hi we are hiring Position;- QC Officer & Executives QC Officer & Executives Location- Baddi Experience- 2-6 years (HPLC analyst ) Salary Range- 20-30 K Interested candidate Apply Mail ;-Tisha.singh@unitedgroupmail.com Contact No;- 9041666549

Job Description Lab Technician Location: Sunfrio Chemical Plant, Gujarat Department: Quality Control / R&D Reports To: Lab Manager / QA Head Employment Type: Full-Time 1. Position Overview The Lab Technician will be responsible for conducting routine and advanced laboratory tests to ensure the quality and consistency of raw materials, in-process materials, and finished chemical products. The role involves analytical testing, documentation, equipment handling, and adherence to safety protocols within the chemical plant environment. 2. Key Responsibilities A. Laboratory Testing & Analysis Conduct qualitative and quantitative analysis of raw materials, intermediates, and finished products. Perf...

Responsibilities: * Conduct HPLC, GC & UV analyses under supervision. * Maintain quality control procedures and documentation. * Ensure compliance with industry standards. Health insurance

As a Sr. Executive / Asst. Manager at our company in Ahmedabad, you will be responsible for the following key duties: - Monitoring the team for raw material sampling and analysis on a daily basis - Troubleshooting and resolving issues during the analysis of raw materials by analysts - Handling the Raw Material section, starting from sampling to the release of raw materials - Demonstrating knowledge of ERP and LIMS - Conducting chemical tests and HPLC analysis - Managing Quality Management Systems (QMS) including incidents and Out of Specification (OOS) results - Providing guidance to ensure compliance with regulatory norms Qualifications required for this role include: - Minimum 12-15 years ...

Job Description: We are looking for a QC Reviewer with strong expertise in reviewing analytical data and ensuring compliance with GMP and data-integrity standards. Key Responsibilities: Review analytical raw data , instrument printouts, chromatograms, logbooks, worksheets, and COAs. Review HPLC analytical data generated for raw materials, intermediates, finished products . Verify that all results comply with SOPs, STPs, and regulatory requirements. Ensure documentation accuracy as per ALCOA / ALCOA+ , cGMP, GLP guidelines. Review results from HPLC, GC, UV, IR, KF, Wet Chemistry and other analytical techniques. Support OOS, OOT, deviation investigations by providing analytical review inputs. ...

Role & Responsibilities Lead development of device coatings with and without drug-eluting capability for medical applications. Formulate and optimize polymer matrices for device coating and for controlled release from device coatings. Design and synthesize sodium-based and acid etching solutions for surface treatment and functionalization. Develop surface modifying reagents tailored for L-605, Nitinol, and other medical-grade alloys. Oversee wet chemistry lab setup including equipment specification, layout, and compliance setup. Establish lab SOPs and ensure strict adherence to EH&S and GLP standards. Plan and execute in vitro drug release studies, stability protocols, and surface characteri...

Roles and Responsibilities Conduct quality control tests on raw materials, finished goods, and in-process samples using techniques such as HPLC, UV, PH meter, etc. Perform calibration of analytical instruments like GC, HPLC, UV spectrophotometer, etc. to ensure accuracy and precision. Ensure compliance with GLP guidelines during sample collection, handling, and testing. Collaborate with cross-functional teams to resolve any issues related to product quality or contamination. Maintain accurate records of test results, instrument calibrations, and inventory management.

Role & responsibilities * Instrumental analysis i.e. GC, HPLC, UPCL, PH meter. * Chromatographic analysis of raw material, finish products, intermediates. * Knowledge about Empower 3 software * Follow good laboratory practices (GLP) in quality control department. * To prepare the COA of API & intermediate material

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: QC Quality Control Experience: (02 07 Years) •HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC/ Micro-biology ARD - OSD Experience: (02 06 Years) •HPLC/ FG/Analytical Method validation/ Stability PACKING Experience: (01-06Years) •Blister Packing, Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) PRODUCTION Experience: (01-06Years) •Compression, Granulation, Coating, QUALIFICATION : ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B. Pharm, M.Pharm with relevant experience DESIGNATIONS: Operator, Jr. Officer, Officer & Jr.Executive NOTE: Offering a Joining bonus only for QC Depart. for Immediate Joiners Instrument experience in HPLC / GC ...

Executive - Sr. Executive - QC - API Responsible for Events (OOS/OOT/Deviation and Laboratory Incidents) investigation. Evaluation of root cause, CAPA, QRA and Investigation report. Preparation/closure of events within timeline to meets the balance between cGMP requirements and business need. Must be having experience in API . Officer - Sr. Officer - QC - API Experience in Sampling of material. Wet testing. Hands on HPLC instruments. Worked in regulatory environment. Must be having experience in API .

Executive - Sr. Executive - QC Responsible for Events (OOS/OOT/Deviation and Laboratory Incidents) investigation. Evaluation of root cause, CAPA, QRA and Investigation report. Preparation/closure of events within timeline to meets the balance between cGMP requirements and business need. Must be having experience in API or Formulation Officer - Sr. Officer - QC Experience in Sampling of material. Wet testing. Hands on HPLC instruments. Worked in regulatory environment. Must be having experience in API or Formulation