222 Wet Analysis Jobs - Page 2

Title: Officer - Formulation QC Custom Field 2: 2691 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Basic knowledge of Formulation QC related activities like Dissolution, Disintegration, Wet analysis Job Segment: QC, Quality

Role & responsibilities Job Summary: We are hiring for multiple QC positions across HPLC, Wet Lab, GC, Stability, QMS/GLP, AMV/PV, Microbiology, Packing & Documentation. Open Positions: QC HPLC: Reviewer / Operator / Preparator QC Wet Lab: Reviewer / Analyst / GC Operator QC Stability: Reviewer / Analyst QMS & GLP: Reviewer QC Packing: Analyst QC Documentation: Computer Operator Raw Material Sampling: Contract (Casual) Microbiology: Analyst QC AMV/PV: Reviewer / Analyst Responsibilities (Common Across QC Roles): Perform analysis as per SOP and quality standards. Review analytical data, reports, and documentation (where applicable). Operate instruments: HPLC, GC, IR, KF, UV, etc. Maintain GLP...

Perform analysis of raw, in-process & finished goods. Operate GC, HPLC, UV, KF, IR. Maintain records, follow GLP & SOPs. Support method validation. Ensure ISO/regulatory compliance & coordinate with QA/production for batch release.

Perform analysis using GC, HPLC, UV, KF & wet methods. Ensure GLP, timely reporting, data review, instrument calibration & method validation. Handle OOS, guide juniors & coordinate with QA/production for batch release. Ensure SOP/ISO compliance.

Operate instruments such as HPLC, GC, UV, FTIR, Karl Fischer , etc. Conduct stability studies .Maintain analytical documentation, COAs, logbooks, etc. Perform instrument calibration

Well Knowledge Handling of HPLC, GC, UV, FT-IR and Wet Analysis, Documentation for Q.C Role & responsibilities Preferred candidate profile

Walk-In Interview Date: 27th to 29th November 2025 (Thursday to Saturday) Timing: 09:30 A.M. to 4:00 P.M. Venue: Amoli Organics, (A division of Umedica Laboratories Pvt. Ltd.), Plot No. 322/4, 40 Shed Area, GIDC, Vapi 396195 1. Production Department Position: Officer Production Qualification: B.Sc./M. Sc. Chemistry/ B.E./B.Tech Chemical Experience: 0 to 5 years No. of Vacant Position: 20 2. Production Department Position: Associate Qualification: B.Sc. & Diploma in Chemical Engg Experience: 0 to 3 years No. of Vacant Position: 10 3. Production Department Position: Apprentice Qualification: B.Sc Chemistry Experience: Fresher No. of Vacant Position: 20 4. Quality Control Position: QC Officer Q...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

hands-on experience in routine wet lab testing of limestone, lime, and related mineral samples, including sample preparation, filtration, weighing, and titration.basic instruments and equipment such as an Analytical balance, a colourimeter, Glassware Required Candidate profile Laboratory experience, preferably in a mining, minerals processing, or metallurgical environment. Experience with instrumental analytical techniques (e.g., AAS, ICP, XRF)

Role & responsibilities :- Quality Control Executive Preferred candidate profile 5 to 7 years of experience in Quality Control Hands-on experience in handling and calibration of instruments such as HPLC, GC, pH Meter, etc. (mandatory) Proficiency in wet analysis Perks and benefits :- 4 to 5 lakh per annum

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

Sr. Executive / Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5-8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/...

Role Overview: You will be responsible for conducting bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Additionally, you will develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaboration with cross-functional teams to ensure timely delivery of high-quality results and performing stability testing of biological products under various conditions will also be part of your role. Troubleshooting issues related to instrument calibration, maintenance, and operation will be an...

Designation - QC Officer / Qc Execitive / QC Chemist / Sr.QC Executive Job Location - Dajej Candidate Experience - 4 to 7 Years Salary - As Per Best Industry Standard Facility - Travelling + Canteen + Medicaim Required Candidate profile GC,LPLC ,WET Chemical Analysis ang Good Knowledge of ISO system & documentation. Perks and benefits Travelling + Canteen + Medicalim

Job Description He should be a good communicator and should know the Analytical techniques liks HPLC,GC ,IR ,UV and Wet analysis Qualifications Master's degree in Analytical/General Chemistry About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirt...

Hands-on experience in HPLC Testing of Raw Material (RM), Packing Material (PM), and Finished Goods (FG) Knowledge of GLP/GMP and documentation practices Ability to handle instruments and perform method validation

Urgent Requirement in PHARMA Industry... Fresher's & Experience persons wanted in QUALITY CONTROL(Wet Analysis / HPLC / GC) Department in Pharma Industry, Candidate should have good working experience in Pharma Manufacturing Units.. Roles and Responsibilities: FOR QC DEPARTMENT In the pharmaceutical industry, the Quality Control (QC) department is responsible for testing and analyzing raw materials, in-process materials, and finished drug products to ensure they meet safety, purity, and efficacy standards. QC Wet Analysis Department (or Wet Chemistry Lab) is responsible for performing traditional, bench-top chemical tests on raw materials, in-process samples, and finished products to ensure ...

Walk-In Interview Date: 14th & 15th November 2025 (Friday & Saturday) Timing: 09:30 A.M. to 4:00 P.M. Venue: Amoli Organics, (A division of Umedica Laboratories Pvt. Ltd.), Plot No. 322/4, 40 Shed Area, GIDC, Vapi 396195 1. Production Department Position: Officer Production Qualification: B.Sc./M. Sc. Chemistry/ B.E. B. Tech Chemical Experience: 0 to 5 years No. of Vacant Position: 20 2. Production Department Position: Associate Qualification: B.Sc. & Diploma in Chemical Engg Experience: 0 to 3 years No. of Vacant Position: 10 3. Production Department Position: Apprentice Qualification: B.Sc. & ITI (AOCP) Experience: Fresher No. of Vacant Position: 20 4. Quality Control Position: QC Officer ...

DEPARTMENT/FUNCTION: Quality (Chemical Lab) JOB SUMMARY As a Lab Technician, you will be performing analytical methods and administrative tasks required to control the quality of our raw materials, finished products and manufacturing processes. The results generated in the QC lab are used to monitor and adjust chemical processes and to the quality of products shipped to our customers. A. DUTIES AND RESPONSIBILITIES Understand and conduct routine tests and analyses used in the QC lab. Analyze data from laboratory and plant operations. Hands on experience in XRF and XRD. To conduct Wet analysis. Provide accurate and timely results of testing. Provide information or instructions to plant proces...

Hiring For QC & QA API Pharma Dept in Jhagadia Company Bsc / Msc Chemistry 4.0 LPA 1 to 7 yr consider Apply : sdpbharuch@gamil.com Sub : QC & QA Dahej Required Candidate profile Interview Date : 14-11-2025 Venue SDP HR SOLUTION ,11, Golden Square, Beside DMart, Near ABC Circle, Bholav, Bharuch, Gujarat 392001 Whatsapp Group : https://chat.whatsapp.com/Hd6iI5PjXVD6iMr09NZ8Oe

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

candidates should have hands-on experience in routine wet lab testing of limestone, lime, and related mineral samples, including sample preparation, filtration, weighing, and titration. Basic instruments and equipment, such as an Analytical balance. Required Candidate profile should have good exposure in the wet lab testing of limestone, lime, and related mineral samples, including sample preparation.

Testing of incoming raw material Standardization of Solution Testing of in process tests samples Testing of Finished Product as per Specification Qualification (IQ, OQ, PQ) and Calibration of QC instruments Preservation and Disposal of Samples safe work practices and Good Housekeeping in the Laboratory. Preparation of Purchase Indent of Glasswares, Chemicals and other Auxiliaries. Internal Communication with Production, Marketing and concerned Department. ERP entry work Preparation of SOP, protocols and other documents. Knowledge of 21 CFR part 11

1) Testing in-coming raw materials material (Non ferrous Metals) and finished product (Non-ferrous oxide) for all parameters. 2) Data entry and record keeping as per quality SOPs and ISO standards 3) Reporting to the QC Head on analysis results Required Candidate profile BSc (minimum) with 4-5 minimum years of experience in analytical chemistry and lab testing, lab instrument handling.