44 Wet Lab Jobs

Role & responsibilities Sample testing Documentation equipment calibration Preferred candidate profile Qualification -MSc in chemistry is must . Must have experience in Pharma - API industry or Testing laboratory . Must be have having good experience in HPLC , GC ,Wet analysis , Stability , Finished products ,Raw - Material .

HPLC -GC Analysis and Reporting, Perform and Monitoring Total Lab Activity, wet lab Analysis , Create and maintain documents for Routine Operation. work distribution and team work, Monitor calibration and preventive maintenance Required Candidate profile Must Efficient hand on HPLC- GC analysis. Problem solving in HPLC, GC and wet lab analysis, having exp. of wet analysis like Titration, gravimetry, UV, Polarimetry, water analysis

Post- Lab Technician Location - Pune Urlikanchan Factory Contact - 9356395439 Education: A post-secondary education (degree and/or diploma) in a science-related field (e.g., Chemistry, Geology, Mining Engineering) is often preferred. 2 -aboratory Experience: Prior experience in a laboratory setting, sample preparation and analysis techniques, is highly desirable. 3 -Sample Handling and Preparation: Sampling, sorting, and labeling samples. Crushing, pulverizing, splitting, and sieving samples according to established procedures. Preparing samples for analysis using various techniques (Wet analysis).

Department - Quality Control Experience - 2 to 5 years Qualification - M.Sc chemistry (Full time) Section - HPLC / GC / Wet lab 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 inward register / LIMS as required for assigning analytical reference number and to store at recommended storage condition until completion of the analysis. To operate and maintain laboratory equipment/instrument as per analyst qualification program. To ensure that entries in log books are made where ever instruments are used in the analysis. To perform all associated activities (bench reagents, indicators, volumetric solution preparation, factor determination etc.) required for sample testing by following the approved procedures. To perform analysis (Chemical) to qualify working standards against reference standard /certified standard/ primary standards. To ensure all primary standards/working standards/certified standards/reference standards are stored as per the storage conditions specified and documented. To check the availability of analytical resources like chemicals/reagents / standards etc. before start of the analysis. To take online print and perform data punching in the LIMS. To monitor temperature of laboratory daily. To send those samples to outside laboratory for analysis for tests not able to be carried out in laboratory. To maintain and ensure controlled laboratory practice in the quality control department. To document the raw data as per current GDP. To follow the SOPs of Quality control department and related area. To follow Specification, STP, GTP and protocol during analysis. To use applicable PPEs (personal protective equipment) while performing testing in the laboratory / during handling hazardous solvents/chemicals. To keep himself updated with current regulatory requirements and train the subordinates and colleagues for day to day activities as well as regulatory. To keep the things and his work area clean and tidy and get involved for the routine trouble shooting (if any). To ensure up-keeping of the instrument/equipment. To ensure laboratory inventory management. To inform section head any incident/ OOS/ OOT/ OOC on its immediate occurrence and for day to day activities. To investigate incident/ OOS/ OOT/ OOC (if any) under consultation with the department head/section head. To perform the analysis of stability samples as per the analyst qualification, requirements and respective procedure. To perform the calibration of instrument as per the planner and / or as and when required. To manage all standards for issuance and its usage. To co-ordinate with in-house service engineers and / or external service engineers as and when required. To ensure the destruction of remnant samples after analysis as per applicable procedure. To perform analysis at CHL inter locations whenever required. Responsible for implementing company quality ethics policy for data integrity and inform management and responsible data integrity compliance head on any data integrity issues as per corporate data governance policy. To escalate any issues related to discipline, availability of manpower, hygiene, contamination, cross contamination, Incidents or deviations, malfunctioning of equipments, any unusual observations, any safety risk or quality risk to next level or in absence further up. To perform any other activities as assigned by HOD after completion of the necessary trainings as applicable.

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-7 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/ In process / 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. HPLC Analyst: Carry out HPLC testing for assay, related substances, dissolution, and stability samples. Operate and maintain HPLC systems (Waters, Agilent, Shimadzu) with appropriate software (Empower/Chromeleon). Prepare standard and sample solutions as per SOPs and approved procedures. Document and report results with accuracy and clarity in analytical worksheets, logbooks, and LIMS (if applicable). Ensure compliance with GMP, GLP, and ALCOA+ data integrity principles. Perform regular calibration and maintenance of HPLC instruments. Support OOS/OOT investigation and participate in deviation handling and CAPA implementation. 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.

Role & responsibilities Should able to handle HPLC & GC,PH Meter, Knowledge on GMP&GLP Preferred candidate profile Familiarity with analytical testing techniques using HPLC/GC/FTIR/Dissolution/UV. Performing calibration of instrumentations Testing of finished product, raw materials, packaging and stability Perform analytical testing - HPLC, FTIR, UV

Job Description: 24 7 audit readiness. 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. Supporting to share required documents from QC to RA/ other requirement. Determining team priorities in accordance with the plants needs, while coordinating with the team leader /Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / 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. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers / autoclaves / incubators. Responsible to work in shift as per requirement. Help to in charge in preparation of documents related to department (like STPs, SOP’s and etc.) Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. 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 Qualifications: Preferred experience with Wet lab instruments/techniques including but not limited to KF Titrator, Auto-titrator, analytical balance, FTIR, Polarimeter, UV, X-ray Diffraction, etc. At least 5-years of relevant experience with Master of science (Chemistry).

Role & responsibilities : Product Inspection Testing & Analysis Documentation Deviation Handling Process Improvement Preferred candidate profile Candidates must have a degree in Bsc /MSc in chemistry with 2 to 4 years of experience in Quality control department ,API Industry. ( Only Male candidates can attend interview )

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&D teams in routine and special analysis projects. Candidate Profile: Education: B.Sc. in Chemistry (mandatory) Experience: 1- 2 years in instrumental analysis (GC and HPLC expertise required) Skills: Strong analytical ability, attention to detail, and familiarity with laboratory documentation Availability: Immediate joiners preferred Job Location: Palghar, Maharashtra

We're Hiring! Assistant Manager Quality Control Location: Hosur | Company: Global Calcium Unit III Experience: 712 years | Full-time | On-site Global Calcium is looking for a passionate and experienced Assistant Manager – Quality Control to join our team at Unit III in Hosur. In this role, you'll be responsible for leading day-to-day QC operations — from testing and inspecting materials to ensuring regulatory compliance, analyzing trends, and driving quality improvement initiatives. You’ll collaborate with production teams to proactively address and resolve quality issues. What We’re Looking For: Strong background in Quality Control with leadership experience Knowledge of regulatory standards and QMS (Area Qualification, Analytical Method Validation, Instrument Qualification) Hands-on experience with instruments like ICP-MS and AAS Excellent analytical, documentation, and problem-solving skills Proficiency in team communication and management Master’s degree in Chemistry, Pharmaceuticals, or related field Prior experience in the pharmaceutical or manufacturing industry is a strong plus Interested candidates can share their profiles at: dhanushkumar@globalcalciumpharma.in Join us at Global Calcium and be a part of a company committed to quality, innovation, and growth.

Qualification :- M.Sc Chemistry Experience :- 0 to 3 year in Pharma or Chemical Company Location :- Jarod ( Vadodara ) Related Experience in HPLC , GC , Wet Analysis

Role & responsibilities passionate about textile chemistry. Experience in wet lab dipping Preferred candidate profile Lab Technician cum Colorist-Washing/Dyeing Unit

Analytical test including physical and wet analysis. Expertise in handling of HPLC, GC , UV and IR Knowledge on OOS and OOT Calibration of laboratory Instruments. Preparation and standardization of Reagents/Volumetric solutions. To ensure cGLP compliance and Data Integrity

Look after overall activities of wet analysis / chemical lab. Responsible for analysis and reporting of Pharma / Ayurvedic / Homeopathic / Cosmetic / FMCG products. Review and evaluate feasibility of projects / samples received from customers. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in or any more information call on 9870476784

Hi Jobseeker, Greetings from Laurus Labs Ltd! Please find the below current openings at Laurus Labs Ltd- Visakhapatnam (Atchutapuram OSD Formulation Unit-2) Department : Quality Control-OSD Formulations Designation : Asst.Manager/Manager Section : Wet Chemistry & Dissolution Interested candidates can send their resume to seetaram.y@lauruslabs.com and please send the below details for further process. Total Exp : Current CTC : Expected CTC : Notice Period :

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of general lab SOPs and instrument sops. Desired candidate profile: 1. Must have worked analytical lab. 2, Knowledge of HPLC,

Key Responsibilities / Skills Required: We require a Q.C. Chemist for our chemical manufacturing plant located at Vatva, Ahmedabad . The ideal candidate should have hands-on experience with: Wet lab operations & basic titration UV Spectrophotometer Karl Fischer titration pH meter handling Moisture content, NV, and LOD analysis

R & amp; D Leadership Quality Assurance (QA) efforts within the dry lab. Laboratory Management: including human resources, payroll, and budget management. Key Responsibilities: Oversee all operational aspects of the dry lab, wet & quot; ink.

Hi Jobseeker, Greetings from Laurus Labs! Please find the below positions of current openings at Laurus Labs - Visakhapatnam (Atchutapuram OSD Formulation Unit) Department : Quality Control-OSD Formulations Designation : Associate/Executive Section : Wet Chemistry & LC-MS/GC-MS Interested candidates can send their resume to seetaram.y@lauruslabs.com and please send the below details for further process. Total Exp : Current CTC : Expected CTC : Notice Period :

Role & responsibilities Profile: QC Sr. Chemist/ QC Officer to Senior Officer for Active Pharma Ingredients Industry in Samba (Jammu). Distance from Pathankot(Punjab) to Samba (Jammu) Manufacturing Unit is 50Kms away. No. Of Positions - 8(QC Chemist/ QC Officer/ QC Executive/QC Sr. Executive) Mandate Qualification - B.Sc/ M.sc Chemistry Experience - 2-10years Knowledge of Instruments- HPLC, GC (Gas Chromatography), UV Spectrometer, Kal Fischer and Experience of Wet Lab Knowledge of GMP and cGMP and Safety of their concern area. Preferred candidate profile: Candidate required only from API Industry from Pharma Industry. Early Joiner will be preferred for this position

Posted On 04th Jun, 2025 : The candidate will be primarily responsible for laboratory testing and R&D activities both in the lab and on the plant floor. The role involves developing and implementing testing procedures for new products, ensuring compliance with ISO 9000 standards, and maintaining accurate records and documentation. Key Responsibilities: Conduct lab-based testing and support R&D activities within the lab and plant environment. Develop and implement testing protocols for new and existing products. Maintain and update all ISO 9000 documentation and records related to lab activities. Coordinate with the designated ISO representative (e.g., Mr. X) for documentation control and compliance. Perform product testing with high precision (required accuracy0.2%). Carry out regular titration tests (approx. 80% of lab work) , and tests using instruments such as pH meters, TDS meters, NTU meters, etc. Ensure timely calibration and maintenance of lab instruments. Support the R&D function through effective internet-based research. Required Skills & Qualifications: Strong foundation in inorganic chemistry , particularly in wet lab testing. Hands-on experience with titration methods and chemical testing procedures. Familiarity with lab instruments such as pH meters, TDS meters, NTU meters, etc. Accuracy-oriented approach with an emphasis on result precision and compliance. Knowledge of calibration procedures for lab instruments. Proficiency in basic computer applications MS Word, Excel, Outlook, and PowerPoint. Ability to browse and research effectively for R&D purposes. Should possess an Android smartphone for operational support and communication. Basic proficiency in reading, writing, and understanding English; fluent spoken English is not mandatory. Location of Job At our factory, Changodar Bavla road, Dist-Ahmedabad Key Skills : Company Profile One of the leading companies in the chemical industry in Gujarat. With over six decades in the industry, they have not only established a strong presence in the domestic market but also built a long list of satisfied clients in more than 18 countries. Their products cater to various industries, including the oilfield industry, photographic ---, pharmaceutical raw materials, textiles, food processing, leather, industrial detergents, and metal finishing Company isregistered with The Gujarat Chamber of Commerce & Industry (GCCI), FIEO, CHEMEXCIL, FSSAI, SSI, NSIC, and GPCB. Above all, They are an ISO 9001-2015 certified company.

Department : Analytical R&D Open Positions : LCMS, HPLC, Wet Lab, Solid state characterization and DQA Work Locations : Shameerpet, Hyderabad Job Description: Need to have strong theoretical knowledge (HPLC/LCMS/WETLAB) Plan and conduct the analysis with required skills. Record the observations meticulously and update to the TL/SME. Share and discuss the observations with supervisor. Independent in maintaining the instrument and setting up the instrument for analysis. Expected to be aware of basics in analytical chemistry (basic analytical techniques Theory and application) as well as handling of laboratory equipment / instruments with basic understanding. Expected to be aware and working in a safety compliant manner

JOB DESCRIPTION: Department : Quality Control - API (Wet Analysis) Position : Officer Executive Experience : 01 to 05 Years Qualification : M. Sc in Chemistry Perform wet chemical analysis, including: Karl Fischer titration (KF) Potentiometric titration pH Measurements Particle Size Distribution (PSD) using Malvern Carry out daily calibration of laboratory instruments such as balances and pH meters. Ensure compliance with standard operating procedures and regulatory requirements. Maintain accurate records of all testing and calibration activities. Interested Candidates please send me resumes to pitchireddy.t@hetero.com

Manage QA/QC across textile processes, support NPD, run wet/dry labs, conduct lab-scale dyeing/printing, ensure quality in woven/knit/denim/non-woven and garments, maintain chemical records, optimize processes, and coordinate with shopfloor teams.

Role & responsibilities Responsible for compliance as per 9001:2015, ISO 14001:2015, ISO 45001:2018. Responsible for validation/ verification of Analytical Methods on ICP-MS, AAS, HPLC and instruments as per ICH Q2 (R2). Responsible for development of Cost-effective, rugged and robust analytical methods on ICP-MS, AAS, HPLC, and wet lab instruments as per ICH Q14 and Analytical QbD. To maintain GLP compliance as per OECD or other regulatory/ general guidelines in ARD lab. Responsible for performing technology transfer of analytical method in QC(Plant). Any other responsibility assign by ARD head, time to time on need basis. Preferred candidate profile Post graduate (M.Pharma/M.Sc) Must be from Pharmaceuticals (preferably API) background.