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3.0 - 6.0 years

3 - 4 Lacs

Ahmedabad

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Candidate must have experience from chemical manufacturing industry.

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3.0 - 6.0 years

3 - 5 Lacs

Jhagadia

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1) Working as per company / management policy & reporting to Quality Control Head. 2) To sample the incoming Raw materials and packing materials and also Finished Goods. 3) To conduct analysis and testing of Raw Material, Packing Material, In-Process sample, Finished goods, Stability samples etc. with the help of analytical instruments and techniques. 4) To calibrate / verifies analytical instruments like HPLC, GD, ICP-OES Wet lab and balances 5) To trouble shoot analytical instruments. 6) Preparation and standardization of Volumetric Solution. 7) Preparation and maintenance of records for stock / reagents. 8) Analysis of samples for qualitative and quantitative test parameters as per specification. 9) To maintain record of analysis and supporting logbooks as per GLP. 10) To have working experience in shift for supporting production activities by analysis of in-process samples. 11) To participate in laboratory investigation. 12) To checked by the In-Process analysis results.

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2.0 - 5.0 years

3 - 4 Lacs

Vadodara

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• Job Opening for Officer / Sr. Officer – QC / ADL having 2 to 5 Yrs Experience in any API / Intermediate manufacturing company near Vadodara. • Hand on Experience in HPLC & GC • HS Wet Lab & Documentation

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1.0 - 3.0 years

0 - 3 Lacs

Hyderabad

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"Quality Control Chemist wanted. Conduct analytical tests (HPLC, GC, wet analysis), ensure product quality, and adhere to regulatory standards. Analyze data, follow SOPs, and maintain accurate records."

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2.0 - 5.0 years

3 - 4 Lacs

Indore, Durgapur, Belgaum

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Role & responsibilities- Conduct analysis of samples using HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Providing Technical support for internal and external stake holders Being the clear R&D player by working closely with cross-functional teams to drive execution across multiple projects while maintaining and achieving timelines to ensure speed to market. To conduct analysis of samples and provide inputs to R&D/QC teams Required Skill Sets: Hands on experience on HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Experience in analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Fair understanding of ISO/IEC 17025, ISO 9001, ISO14001, ISO 22000, ISO18001 Lab safety & GLP management

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2.0 - 6.0 years

1 - 5 Lacs

Gajraula

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Role & responsibilities 24 7 audit readiness. Exposure in Wet Chemistry. Responsible to works in different shifts. Perform the raw material analysis & wet lab activity by using the technique (KF, pH, KFC, UV, FTIR, SOR, Oven, Auto titrator, Polari meter & TLC) etc. Sampling of Raw material / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. Perform analytical test according to the monograph and SOP. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Participation in internal, external, regulatory audits. Ensure 100% participation in trainings against CAPAs. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader /Manger. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers. Must be ensured sampled, approved, and rejected labels timely as required. Responsible to maintain the stock record of chemicals and reconciliation of standards. Any other job assigned by the Manger -QC Manger or group leader-QC

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0 - 3 years

3 - 6 Lacs

Coimbatore

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Role & responsibilities - Following standard laboratory protocols to develop, test, and characterize tailored Graphene dispersions for various applications. - Preparing detailed reports based on the evaluation of Nanomaterials, utilizing different characterization techniques to ensure comprehensive analysis and documentation. - Identifying and evaluating new methods and processes aimed at simplifying the product development process. - Collaborating and coordinating effectively with the R&D team and other stakeholders to ensure collaboration and timely completion of designated tasks. Preferred candidate profile Terracarb is currently seeking a highly motivated and skilled graduate to join our dynamic R&D team. The successful candidate will play a key role in developing and testing Graphene dispersions, for applications such as paints and coatings, inks, polymer composites, and energy storage. Candidates with prior experience in wet chemistry processes are encouraged to apply. Perks and benefits Salary as per industry standards with eligibility to join ESOP pool for exceptional candidates - - Other standard perks that are part of working in a fast-growing startup are applicable as well

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1 - 3 years

3 - 5 Lacs

Ahmedabad

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Role & responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Preferred candidate profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

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0 - 3 years

0 - 3 Lacs

Ankleshwar

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Role & responsibilities Sampling and analysis as per standard operating process Wear and ensure all helpers adhere to safety PPE s and follow safety standards. If discrepancy found in samples coordinate with Senior Chemist Take samples from inward vehicles and conduct Quick Check analysis Take in process sample for analysis and take corrective measures if not in coordination with Senior Chemist Check all instruments are in working condition and if not inform Senior Chemist Prepare all lab reagents and chemicals as per standards and discard if expired in coordination with Senior Chemist Implement Good House Keeping Practices and keep laboratory clean (5S) Instrument Handling COD- Digester, Oven, muffle, Auto titrator, flame photometer, Bomb calorimeter, PH meter, Conductivity meter, TDS meter, flash point tester Preferred candidate profile 0 to 3 years of experience in Laboratory / Quality control Skill: Instrument Handling COD- Digester, Oven, muffle, Auto titrator, flame photometer, Bomb calorimeter, PH meter, Conductivity meter, TDS meter, flash point tester Perks and benefits Mediclaim (spouse and up to 3 child)

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0 - 5 years

2 - 4 Lacs

Payakaraopeta

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Responsibility: 1. Responsible to ensure safe evacuation of all the employees of the department and report the numbers during emergency. 2. Responsible to follow the GMP, GLP, Safety norms and adhere to companys policy. 3. Plans implementation of Innovative techniques and performs lab rounds to identify gaps in safety and procedures. 4. Assesses safety related risks and guides team in implementation of appropriate procedures to ensure safe working environment. 5. Reviews and enable safety handing procedures in new equipment/ instrument. 6. Ensure the appropriate use of laboratory materials and equipment. 7. Follow the material safety data sheet instruction. 8. Receive the samples from process development department for sampling and to analysis. 9. Preparation of the standard sample solutions by the guidance of Executive and above designee. 10. Responsible for performing routine sample preparation, and laboratory tests or analysis according to provide test method and record the results 11. If any abnormality identified during the analysis Report immediately to the concern person. 12. To follow safety norms and adhere with company policy. 13. To follow the Quality Policy & Contamination prevention policy of the company 14. Follow the cleaning and washing procedures by the guidance of Asst. Manger and above designee. 15. Maintenance of chemicals and HPLC, GC, IC columns in good conditions and ensure the keep at des 16. Ensure all the Systems calibration status before handling of the systems. 17. Responsible for perform the daily calibrations of Analytical balance, pH meter and Karl Fischer reagent apparatus. 18. Responsible for creation of HPLC, GC method as per the provided test procedures, run the sequence and integrating the chromatogram under guidance of Asst. Manager and above designee. 19. Authorized to stop unsafe activities. Preferred candidate profile: Person Should Have M.Sc. Analytical Chemistry With 0 to 7 Years Experience in AR&D and Immediate Joiners are preferred. Positions: Chemist / Sr. Chemist / Executives For More Info Call to 8886311229 Share Your Resume To : tkamaleshkumar.hr@deccanchemicals.com Perks and benefits : PF, ESIC, Bonus, Mediclaim, Transport, Subsided Canteen, GPAP

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2 - 6 years

2 - 3 Lacs

Vadodara

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Quality Control (QC) Officer- Wet lab required for reputed organisation in Vadodara (Gujarat) location Dear Professionals,, I am Sindhura C , from the Pharma Vertical of Masadir HR Services , an International Recruitment Firm. We have been retained by professionally managed organisation to recruit Quality Control (QC) Officer- Wet lab for them. The job location is in Vadodara (Gujarat). Qualification: Bsc/Msc Organic Chemistry Experience: Min 1yr Responsibilities Packing Material Sampling, Analysis & labeling. • Receiving of Packing Material GRN from Stores and its entry in the respective register. • Specification entry in ERP for new Packing Material. • QC registers entry for GRN in ERP & QC analysis update for GRN in ERP system. • Raw Material Sampling, Analysis & labeling. • Analysis of Medicament product, Bulk product and Finish product Analysis. • Daily Water Analysis and Reporting. • Hands on experience handling lab instrument like UV • Prepare Working standard stock solution and its Record. • Preparation & Standardization of volumetric solutions. If you are interested in exploring the above opportunity, kindly share your updated resume with me please. In case, if you are not interested, kindly feel free to refer your friends who may be interested in this. Looking forward to hearing from you soon. Thank you! Have a great day! Warm Regards, Sindhura C Associate| Global Talent Acquisition Operations | India Mobile/ WhatsApp : +91 6282564376 Email Id: sindhura.c@masadirservices.com www.masadirservices.com

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3 - 6 years

5 - 10 Lacs

Vadodara

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Job Responsibilities: 1. Perform analysis procedures mainly bioburden testing, spectrophotometric testing and mechanical studies using UTM machines 2. Ensure product stability studies are completed satisfactorily and supported by correct product sample analysis 3. Also, whenever required provide support to Marketing by educating customer 4. Establish a tracking mechanism for customer & field complaints and suggest corrective actions Profile: 1. You have experience of around 3 or more years in pharmaceutical industry 2. Educational Qualification - M.Sc./M.Pharm degree with strong interest in quality control 3. You work accurately, technically minded and able to work independently after training in the matter entrusted to you. Experience in a formulations/ API industry is an asset

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1 - 4 years

2 - 3 Lacs

Dahej

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Role & responsibilities 1. Operating HPLC and GC 2. Analysis of materials 3. wet lab analysis

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1 - 3 years

1 - 2 Lacs

Navi Mumbai

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JOB DESCRIBTION: Following good laboratory practices as laid down in quality control standard operating procedures. Monitoring of daily temperature and humidity of QC laboratory. preparation and standardization of volumetric solutions. calibrations of QC instruments. analysis of stability study sample and hold time study samples within timeline as per schedule.

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1 - 6 years

2 - 3 Lacs

Vadodara

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Quality Control (QC) Officer- Wet lab required for reputed organisation in Vadodara (Gujarat) location Dear Professionals,, I am Sindhura C , from the Pharma Vertical of Masadir HR Services , an International Recruitment Firm. We have been retained by professionally managed organisation to recruit Quality Control (QC) Officer- Wet lab for them. The job location is in Vadodara (Gujarat). Qualification: Bsc/Msc Organic Chemistry Experience: Min 1yr Responsibilities Packing Material Sampling, Analysis & labeling. • Receiving of Packing Material GRN from Stores and its entry in the respective register. • Specification entry in ERP for new Packing Material. • QC registers entry for GRN in ERP & QC analysis update for GRN in ERP system. • Raw Material Sampling, Analysis & labeling. • Analysis of Medicament product, Bulk product and Finish product Analysis. • Daily Water Analysis and Reporting. • Hands on experience handling lab instrument like UV • Prepare Working standard stock solution and its Record. • Preparation & Standardization of volumetric solutions. If you are interested in exploring the above opportunity, kindly share your updated resume with me please. In case, if you are not interested, kindly feel free to refer your friends who may be interested in this. Looking forward to hearing from you soon. Thank you! Have a great day! Warm Regards, Sindhura C Associate| Global Talent Acquisition Operations | India Mobile/ WhatsApp : +91 6282564376 Email Id: sindhura.c@masadirservices.com www.masadirservices.com

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1 - 6 years

1 - 6 Lacs

Jammu

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We have some requirements in Jammu Plant Profile - QC Qualification - BSC or MSC Experience - 1-6years Salary - Upto 6 LPA Location - Jammu Interview Mode - Virtual #only API Plant Preference meenakshikandpal@tdsjobs.com 9815675900

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1 - 6 years

2 - 5 Lacs

Ahmedabad

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Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-8 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ Inprocess / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career!!! Regards Team HR Unison Pharmaceuticals Pvt. Ltd.

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2 - 4 years

2 - 5 Lacs

Bengaluru

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Responsibilities: Conduct wet analyses and method validations Ensure compliance with industry standards and regulatory requirements Maintain cleanliness and safety protocols in the lab environment Share cvs to ramya_n@hikal.com

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2 - 6 years

2 - 5 Lacs

Bharuch, Dahej

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Essential Skills: Should have knowledge & Experience for Sampling and Testing of Raw Material, Packaging Materials, Intermediates and Finished Products. Major Responsibilities 1) Should have Hands on Experience in Sampling and Chemical Testing of Raw Materials, Packaging Materials, Intermediates and Finished Products. 2) Should have basic knowledge of Volumetric Solution preprations and Standaradizations, Calibrations of Equipments and its required Documentation. 3) Should have knowledge of cGMP, GLP and GHP and should have Hands on Experience of SAP QA Module.

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