79 Wet Analysis Jobs

As a key member of the Quality Control team, your main responsibility will involve performing laboratory analysis and instrumentation tasks efficiently. This will include conducting analytical tests on raw materials, finished products, and various samples within specified timelines. You will also play a crucial role in maintaining control of the data generated from these analyses. To excel in this role, you should possess the following skills: - Proficiency in wet analysis techniques such as titrimetry and other relevant methods - Familiarity with a range of analytical procedures - Hands-on experience in operating instruments for analyzing color, moisture, etc. - Ability to carry out maintenance, calibration, and validation of laboratory equipment - Prior exposure to handling GC/HPLC instruments would be highly advantageous In terms of experience, we are looking for candidates with a minimum of 2-3 years of relevant experience in the food or food-related industry. This experience should cover a broad spectrum of activities related to quality control and laboratory analysis. For more information on our commitment to workplace diversity and inclusion, please visit IFF.com/careers/workplace-diversity-and-inclusion. We look forward to welcoming a dedicated professional like you to our team!,

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

Role & responsibilities 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 Note : Candidate who can Join Immediately are preferred and willingness to work in Shift basis. Candidate should have experience in Pharmaceutical Formulation - OSD - Tablets Manufacturing facility

As an ideal candidate for this position, you must hold a minimum qualification of BSc in Chemistry. Additionally, you should possess a solid experience ranging from 3 to 5 years in the field. Your primary responsibility will involve showcasing expertise in conducting Wet Analysis specifically focusing on low carbon Ferro alloys and minerals. This role requires a keen eye for detail and a thorough understanding of analytical techniques and procedures related to the aforementioned materials.,

The role offers you the opportunity to complete product quality checks under close supervision. You will be responsible for conducting routine testing and analysis of production work, ensuring accuracy in quality checks and documenting quality control issues as needed. Your essential functions will include timely analysis of samples under test, coordinating with production for quality-related issues, sampling and analyzing RM/Intermediate/Finished Goods, ensuring compliance of ATR, assisting in ISO implementation, and possessing knowledge of calibration, standard preparation, standardization, and relevant documentation. Furthermore, you will need to have expertise in handling HPLC, GC, and wet analysis. As part of your department-specific and ongoing functions, you will be required to provide timely reports to SAP for result recording, fill and update all relevant documents, maintain zero accidents in quality operations, achieve batch-wise timelines, quantity, and quality, train and supervise operators in your department, participate in the Emergency response team, and maintain ISO 9001:2008 and ISO/IEC 17025:2005, SAP, and other Quality systems. To qualify for this position, you must hold an M. Sc. in Chemistry and have 3-4 years of experience in Quality, including cGMP, ISO, and regulatory audits, as well as laboratory safety. Preferred skills and qualifications include knowledge of Quality Control in Fine Chemicals and pharmaceutical companies and experience of cGMP. Desired skills and competencies for this role include willingness to learn, being a team player, and possessing good communication skills. Please note that the above statements are a general description of the nature of work performed in this classification and are not exhaustive. Avantor is an equal opportunity employer committed to diversity and inclusion. Join our global team of 14,000+ associates at Avantor and make a difference in people's lives through life-changing science. Dare to go further in your career, contribute your talents, learn new skills, and grow with us. Apply today and be part of a culture that supports your career growth and success. If you require a reasonable accommodation during the employment process, please contact us at recruiting@avantorsciences.com to discuss your needs. Requests for accommodation will be considered on a case-by-case basis. By submitting candidates without a formal assignment or contract from Avantor, you forfeit any fee, as per our 3rd Party Non-solicitation Policy. Avantor engages with recruitment agencies based on its needs and does not accept unsolicited solicitations.,

Job Title: Quality Control Chemist Job Location - Bathinda/ Rajpura, Punjab Job Purpose and Impact The Chemist - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up. Perform method validation and verification to roll out new testing method in the lab. Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system. Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports. Maintain systems and techniques for reporting data across functional areas. Organize and participate ring tests with the goal to check and control methods and equipment. Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff. Other duties as assigned Qualifications Minimum Qualifications Bachelor's degree in a related field or equivalent experience Preferred Qualifications "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively" Necessary English reading capacity Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc. Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing Minimum of Three years of working experience in the Food industry Lab

Walk In Drive For Quality Control Department In Formulation Division @ Burgula Department :- Quality Control Qualification :- BSC | B Pharmacy | MSC | M Pharmacy Experience :- 5 to 6 Years Interview Date:- 30-07-2025 Interview Time:- 9AM TO 2.00PM Work Location: - MSNF-VI,Burgula Venue Address:- X59Q+P95, Mothighanapur, Burgula, Telangana 509202 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter,CTC,Payslips ,Bank Statement, Certificates,Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

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

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.

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.

You should be a good communicator with knowledge of analytical techniques such as HPLC, GC, IR, UV, and wet analysis.,

As a Chemical Lab Officer at Sarigram, you will be responsible for conducting various analytical tasks related to organic, inorganic, and analytical chemistry. With 3-5 years of experience and an MSc in Chemistry, your role will involve performing wet analysis, titration of inorganic materials including acid-base and complexometric titrations, as well as balancing chemical equations. You should also possess the ability to calibrate instruments and demonstrate innovative thinking in problem-solving. Your responsibilities will include the preparation of standard solutions, maintenance of Raw and Rough lab registers, and carrying out instrumental methods of analysis such as Flame Photometry, Refractive Index, and Gas Liquid Chromatography (GLC). Additionally, you will be required to create Certificate of Analysis (COA), specifications, Corrective and Preventive Actions (CAPA), Quality Assurance (QA) documents, Standard Operating Procedures (SOP), Batch Manufacturing Records (BMR), and ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Effective communication skills are essential as you will be handling email correspondence and interacting with various departments. Proficiency in Microsoft tools such as Word, Excel, and PowerPoint is mandatory. A flexible mindset for multitasking will be advantageous in this role to meet the dynamic requirements of the laboratory environment. Overall, as a Chemical Lab Officer, you will play a vital role in maintaining high-quality standards, ensuring accurate analysis, and contributing to the overall success of the laboratory operations.,

The ideal candidate should possess strong communication skills and be well-versed in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis.,

As a member of the New Chemical Entity(NCE) Research team located in Navi Mumbai, India, your primary responsibility will be the analysis of compounds for various projects from the medicinal chemistry team and lead NCEs. Your role will involve ensuring quality output within the set targets established by the Group leader, with approximately 60% of your time dedicated to this task. Another key aspect of your position will be the development of analytical methods for new NCEs using a range of instrumental techniques such as HPLC, LCMS, NMR, IR, SFC, and other wet analysis methods. This will require a high level of proficiency and attention to detail to deliver quality results within the specified targets, accounting for about 20% of your time. Additionally, a good understanding of analytical skills and basic knowledge of HPLC, LCMS, NMR, and SFC instruments will be essential for successful performance in this role. Achieving quality output within the designated targets set by the Group leader will be a core expectation, with approximately 20% of your time allocated to these tasks. Overall, your contributions to the NCE Research team will play a crucial role in advancing projects and lead NCEs, with a focus on maintaining high-quality standards and meeting set objectives under the guidance of the Group leader.,

Perform chemical analysis, testing and quality control. Ensure all instruments are calibrated and maintain records. Prepare and review Standard Operating Procedures (SOPs), COAs. Support audits, documentation, and inspections. Knowledge of ISO, EHS Annual bonus

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

Role & responsibilities 1. Good Knowladge about wet lab analysis. 2. Responsible for QC reviewer. 3. Reviewer in LAB solution, LAB-India software, CDS software, IR, UV, TLC. 4. Knowladge about GC analysis. 5. Responsible for analysis of raw material, finish products, intermediates RM/PM/Finished COA's etc. Preferred candidate profile Candidate preferred pharmaceuticals API manufacturing background. USFAD approved plant background would be advantage.

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,

Hi, Dear candidate, we need bsc,msc,B pharmacy,M pharmacy freshers and experience for QC Deportmen t in reputed pharma company. Note: Follow this link to join my WhatsApp group: https://chat.whatsapp.com/G5T8exrULZ12rbO26hvKBB. Provident fund Health insurance

Role & responsibilities Manager technical is the In-charge of Analytical Division. He/She shall report to the SBU-head about all the activities in the Analytical Division. He/She shall look after all the operations of the Division under the guidance/ supervision of SBU-Head. He/She shall be responsible for the standardization and validation of the test methods. He/She shall be responsible for ensuring the availability of the reference material / working reference standard. He/She shall be responsible for assigning the jobs to the analyst as per their calibre. He/She shall be responsible for checking the calculation part and reporting of the results before sending for authorized signatory. He/She shall be responsible for the smooth operations of the equipments/Instruments. He/ She shall be responsible for signing the test certificate / test reports. He/ She shall be responsible for verifying the outside calibration certificates. He/She shall be responsible for the supervision of technical staff working under him/ her. He/She shall be responsible for filling the change control, deviation control, OOS, CAPA raised by technical department. He/She shall be responsible for the preparing / reviewing the scope as per requirements. He/She shall ensure that the glassware used in his / her section should be duly calibrated or verified as required. He/She shall be responsible for the qualification and calibration of new instruments/ equipment. He/She shall be responsible for the maintaining overall quality as per ISO/IEC 17025. He/She shall be responsible for all the relevant works of VP- Technical/GM Operation in his absence.

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

Company Name: Oneiro Lifecare Pvt Ltd Location: Ekalbara Designation: QC Chemist/Officer/Sr Officer Job description (JD): Qualification: Masters (Chemistry) Candidate should have following criteria: 1] Experience of 1-6years in ADL / QC. 2] Handling instruments like HPLC and GC-Headspace. 3] Handling other analytical instruments like KF-Titrator, Auto-Titrator, pH-meter, Polarimeter, UV Spectrophotometer, Balance etc. 4] Analysis of In-process monitoring, Raw material, Intermediates, Stability studies and Drug substances (API). 5] Analytical method development and analytical method validation exposure. 6] Calibration of analytical instruments 7] Should follow GLP practices, Document preparation for Specifications, SOPs, Certificate of analysis and technical reports. Note: Candidate should be willing to work in shifts and across multiple locations as per organizational needs.

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

Dear Candidate, We are conducting walk-in drive on 05th July (Saturday) 2025 for the positions in our Analytical Research & Development department. Job Description : Position Name: Research Chemist/Senior Research Chemist/Research Associate Experience: 1 to 5 years Qualification: M.Sc Analytical Chemistry/Organic Chemistry/M.pharm Work location: Uppal/Mallapur Walk-in Date: 05th July 2025 (Saturday) Time: 09:00 AM to 12.00 PM Venue:-Plot No. B-11/1,,,IDA Uppal,Hyderabad Key Skills and Competencies: High-Performance Liquid Chromatography (HPLC) Key Skills and Competencies: Operation and Maintenance : Proficiency in operating HPLC systems (e.g., Agilent, Waters, Shimadzu) and performing routine maintenance, calibration, and troubleshooting of equipment issues like pressure fluctuations or detector errors. Method Development and Validation : Ability to develop and optimize HPLC methods for analyzing small molecules, impurities, or degradation products, adhering to ICH guidelines (e.g., ICH Q2 for validation). Data Analysis : Expertise in interpreting chromatograms, quantifying analytes, and using software like Empower or ChemStation for data processing and reporting. Sample Preparation : Skilled in preparing samples (e.g., dissolution, extraction) for pharmaceutical or chemical analysis, ensuring reproducibility and accuracy. Regulatory Compliance : Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for documentation, method validation, and audit readiness. Troubleshooting : Ability to diagnose and resolve issues such as peak tailing, baseline drift, or column degradation. Experience Level (1-5 Years) : 1-2 years: Basic operation, routine analysis, and data interpretation under supervision. 3-5 years: Independent method development, validation, and troubleshooting with familiarity in handling complex matrices. 2. Wet Analysis in Good Laboratory Practices (GLP) Key Skills and Competencies: Classical Analytical Techniques : Proficiency in titration (acid-base, redox, complexometric), gravimetric analysis, and other wet chemistry techniques for assay determination or impurity profiling. GLP Compliance : Strict adherence to GLP standards, including proper documentation, sample tracking, and maintaining a chain of custody for regulatory audits. Standard Operating Procedures (SOPs) : Ability to follow and draft SOPs for wet analysis methods, ensuring consistency and compliance. Quality Control : Knowledge of preparing and standardizing reagents, performing limit tests, and ensuring accuracy in quantitative and qualitative analysis. Safety and Handling : Expertise in safe handling of chemicals, waste disposal, and maintaining a contamination-free lab environment. Data Integrity : Ensuring accurate record-keeping, traceability, and error-free reporting in lab notebooks or electronic systems. Experience Level (1-2 Years) : 1-2 years: Performing routine titrations, standardization, and sample preparation under GLP guidelines. 3. Liquid Chromatography-Mass Spectrometry (LCMS) Key Skills and Competencies: Instrument Operation : Proficiency in operating LCMS systems (e.g., Thermo Fisher, AB Sciex) for qualitative and quantitative analysis, including single quadrupole, triple quadrupole, or high-resolution MS (e.g., Orbitrap). Method Development : Ability to develop LCMS methods for identifying and quantifying trace-level impurities, metabolites, or active pharmaceutical ingredients (APIs) in complex matrices. Mass Spectra Interpretation : Expertise in analyzing mass spectra, identifying molecular ions, adducts, and fragmentation patterns for structural elucidation. Sample Preparation : Skilled in sample extraction techniques (e.g., SPE, LLE) and matrix effect minimization for bioanalytical or pharmaceutical samples. Software Proficiency : Familiarity with LCMS software (e.g., Xcalibur, Analyst) for data acquisition, processing, and reporting. Regulatory Knowledge : Understanding of regulatory requirements (e.g., FDA, EMA, ICH) for bioanalytical method validation and GLP/GMP compliance. Troubleshooting : Ability to address issues like ion suppression, carryover, or instrument sensitivity. Experience Level (1-5 Years) : 1-2 years: Conducting routine LCMS analysis, sample preparation, and basic data interpretation under guidance. 3-5 years: Independently developing and validating LCMS methods, troubleshooting complex issues, and supporting drug discovery or development projects. Interested candidates can attend walk-in drive or share their profiles to saivardhan.kothuri@chemvedals.com