222 Wet Analysis Jobs

Role & responsibilities Lead wet chemical and spectroscopic analysis of ferrous and non-ferrous metal samples . Ensure compliance with IS, ASTM, ISO standards and NABL (ISO/IEC 17025) requirements. Review, verify, and approve test results, calculations, and final reports . Develop, verify, and validate test methods , including establishment of measurement uncertainty . Manage PT / ILC participation , evaluate results, and implement corrective actions where required. Act as Technical Authority and support NABL Technical Signatory activities and audits. Oversee laboratory instruments, calibration, maintenance, and chemical inventory . Ensure compliance with laboratory safety, chemical handling...

GC,PH,KF handling Take A Sample RM and GF from tanker,Drum and Bags. Perform Lab tests as per Required. Perform All Typer Water Analysis and Maintain Proper Record

Role & responsibilities 1) Media preparation and GPT analysis 2) PET Test of OSD products 3) Culture and Bioball Handling 4) HPHV autoclave operation 5) Environmental Monitoring MLT analysis of stability samples, In-Process and Finish product Preferred candidate profile 1) Sound knowledge about the good communication. 2) Good knowledge about the GLP & GDP. 3) Good time management skills. Sound knowledge about the quality management system

Perform quality control testing of raw materials and finished products Conduct chemical analytical testing as per SOPs Maintain QC documentation and records accurately Ensure compliance with GMP quality standards Support the stability studies Required Candidate profile Minimum 1+ years of experience in Quality Control (QC) in a pharmaceutical company

Analyst to Executive(Exp: 2 to 5 Years) :Instrumentation analysis (HPLC, GC, Calibration, Analysis, On line-Documentation, maintain GLP,GDP) Analyst to Sr. Officer(Exp: 2 to 4 Years) Wet lab Analysis like Operation and Calibration of Analytical balances Instrument, Auto Titrator, PH Meter, Coulometer, Halogen moisture analyser, Vacuum oven , Hot air oven, Titrations, Water analysis, Sieve analysis Reviewer/Supervisor (Exp: 5 to 8 Years) Review of online documentation, release of products, Complete Awareness on QMS System, Review of calibrations, Analytical records, Daily work planning and implementation. Analyst to Sr. Officer(Exp: 2 to 4 Years) Analysis of Stability samples, Initiation and ...

As a part of the QC Department at Global Calcium Pvt. Ltd., a leading pharmaceutical manufacturer, you will have the opportunity to contribute to quality and innovation. We are currently hiring for multiple roles, including QC ICP-MS Analyst, QC DMF Support, QC Analytical Validation Support, and QC Wet Analysis. Join us in our commitment to excellence and be a part of a dynamic and growing team. Key Responsibilities: - Conduct routine and non-routine analyses using analytical techniques and instrumentation. - Develop and validate analytical methods and protocols. - Prepare and maintain detailed documentation and reports. - Ensure compliance with regulatory guidelines and GMP standards. - Col...

Roles and Responsibilities Conduct quality control tests on chemicals, raw materials, intermediates, and finished products using techniques such as wet analysis and chemical testing. Stability studies -analysis , documentation , sample preparation and withdrawal Maintain accurate records of test results, inspection reports, and other relevant documentation. Collaborate with cross-functional teams to resolve quality issues and improve product performance.

We are seeking an experienced and dynamic Quality Control Manager-Formulation to lead QC operations for pharmaceutical formulations. The role ensures product quality, regulatory compliance, and effective laboratory management across formulation units

Role Overview: You will be responsible for operating HPLC and GC independently. Additionally, you are expected to have a good understanding of basics in analytical chemistry, including basic analytical techniques, theory, application, and handling laboratory equipment. Your role will involve independently planning, handling, and analyzing regular samples using HPLC/GC. Awareness of other techniques such as wet analysis and spectroscopy is also required. As a valuable team member, you should be a good team worker. Knowledge of GLP/cGMP-WHO and safety practices, as well as familiarity with GLP and cGMP-WHO documentation, are essential in this role. Key Responsibilities: - Operate HPLC and GC i...

Job Responsibilities Perform routine and non-routine chemical analysis and quality testing of dyes and pigments. Ensure all products meet established quality standards and specifications. Conduct wet analysis, titrations, sampling, and testing of raw materials, intermediates, and finished goods. Operate and maintain laboratory instruments such as pH Meter, UV, GC, HPLC (as applicable). Maintain accurate test records, analytical reports, and documentation as per QC guidelines. Ensure adherence to lab safety protocols and standard operating procedures (SOPs). Support process improvement activities and coordinate with production for quality-related issues. Skills Required Strong knowledge of dy...

Role Overview: As a Scientist at USP, you will play a crucial role in conducting analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your expertise will enhance the laboratory's scientific proficiency and work ethic by providing technical support and knowledge. You will be proficient in various laboratory techniques and capable of offering valuable observations and insights into challenging projects. Your responsibilities will include executing analytical tests, preparing summary reports, and contributing to the Verification Program. Key Responsibilities: - Conduct verification projects on Dietary Supplements/Dietary Ingredients by perfo...

Role Overview: As a Scientist at USP, you will be responsible for conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your role will involve enhancing the laboratory's scientific proficiency and work ethic by providing extensive technical support and knowledge. You will be proficient in various common laboratory techniques, offering valuable observations and insights into challenging projects. Your primary responsibility will be to provide technical aid to the Verification Program by executing analytical tests and preparing comprehensive summary reports. Key Responsibilities: - Conduct verification projects on Dietar...

Company: Botanic Healthcare Job Title: QA/QC Executive / Officer / Analyst Department: Quality Assurance / Quality Control Location: Nacharam & Choutuppal (Hyderabad) Reporting To: QA/QC Manager Role Overview Responsible for quality control testing, documentation, GMP implementation, raw material evaluation, and ensuring compliance with regulatory & customer standards for herbal extracts and nutraceutical products manufactured at the Nacharam site . Qualifications & Skills B.Sc / M.Sc / B.Pharm / M.Pharm (Chemistry, Botany, Microbiology, Biotechnology, etc.). 18+ years of QA/QC experience in herbal extracts, nutraceuticals, API, food, or phytochemical industry . Knowledge of GMP, GLP, docume...

Wet Analysis, Intrumentation( IR, Polarimeter, Melting point apparutus), QMS Handling Knowledge. Required Candidate profile Requried Candidates from API Pharma

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...

Vipul Organics Limited (VOL) is a leading manufacturer of specialty chemicals and colorants, committed to innovation, quality, and environmental safety. With a strong legacy and global presence, we are now looking to strengthen our team with a dedicated Instrumentation Chemist at our Palghar unit. Key Responsibilities: Conduct precise chemical analysis using Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC) . Ensure regular calibration, maintenance, and troubleshooting of GC and HPLC instruments. Record, analyze, and report test results in a timely and accurate manner. Maintain laboratory standards as per safety, regulatory, and quality protocols. Support the QC and R...

Job Description: You should possess strong communication skills and be well-versed in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis. Key Responsibilities: - Demonstrate expertise in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis. - Communicate effectively within the team and with stakeholders. Qualifications Required: - Strong communication skills. - Proficiency in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis.,

We are looking for Quality Officers with hands on experience of chemical industry.

Walk-In Drive for Multiple Positions at Daicel Chiral Technologies (India)Limited Department: Pharma Standard - AD Job role: Trainee Chemist/Sr. Chemist / JRA Experience: 0-4 Years Required Qualification & Experience & Skills: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 4 Years of experience in the field of pharmaceutical industry/CRO setup. Develop preparative suitable methods by HPLC & SFC . Execution of Chiral separation, Purification and impurity isolation activities by preparative HPLC, SFC, LCMS. Expertise in Purification of peptides, Oligonucleotides impurity isolation. **************************************************************************** Department: Pharma Sta...

Must be good in Chemistry and Wet tests. QC different modern apparatus exposures and SAP knowledge preferred. Must understand basics of dry and Tests, QC methods and documentation, Incoming RM and finished goods Q.C. experience, COA exposures. Required Candidate profile Must be a good student of Chemistry with understanding of name Reactions, Elements detection, use of ultra modern techniques of QC Perks and benefits Mediclaim Canteen Transport learning & fast career

Sampling of finished products as per SOP. Ensuring cleanliness of sampling devices and glasswares as per the procedure Following good laboratory practices and safety measures Maintenance of control sample as per the procedure Maintenance of laboratory cleaning as per the procedure Personal safety and environmental concern should be applied at work at all times Preparation of market sample based on the market requirement and maintenance of packing material in Stock Preparation of COA and maintenance of all analytical records. Preparation of approved label and maintenance of control register Reagents, chemical and glassware stock maintenance. Preparation of SOP, Specification and related docum...

Role & responsibilities 1) Sampling and testing of Raw material, Packaging material, in process samples and finished products as per specification and standard testing procedure. Testing of water samples as per defined sampling frequency. 2) Preparation of laboratory reagents and volumetric solutions required for chemical analysis in the laboratory. 3) Preparation of SOP (standard operating procedures), EOP (equipment operating procedures), protocols, STP (standard testing procedures) and specifications for the in-process samples and finished products as per customer requirement. 4) Calibration of the laboratory instruments as per the equipment operating procedures. 5) Appropriate record kee...

Role & responsibilities Analysis of raw materials, in process, intermediates, finished product, stability samples Operate and calibrate instruments like HPLC, UPLC, GC, Potentiometer, UV-Visible spectrophotometer, pH meter etc. Prepare / planning sampling and to send issuance request of formats, protocols, reports required for analysis Experience required from API & Bulk Drug, Prepare the standard operating procedures and calibration procedures SOPs of Lab instruments.

1.Conduct analysis of raw materials, intermediates, and finished products. 2.Operate analytical instruments like HPLC, GC, UV, and IR. 3.Ensure compliance with GMP, GLP, and company quality standards. 4.Maintain test records

Proficiency in HPLC, GC, and Wet Analysis, Hands-on experience with method validation and stability studies, Familiarity with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), Exposure to handling regulatory audits such as USFDA, MHRA, and other global agencies, Ability to analyze and interpret complex data with attention to detail