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3.0 - 5.0 years

7 - 11 Lacs

Gurugram

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Senior Chemist-Residues Analysis of Pesticide residues in Food and Feed samples. Operation and Maintenance of LC-MS/MS and GC-MS/MS. Reference standards maintenance. Calibration of LC-MS/MS and GC-MS/MS. Recording and maintenance of temperature and humidity sheets. Calibration of Maintenance of micropipettes and analytical balances. Preparation of standard stock and working solutions. Qualifications M.Sc Chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

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2.0 - 3.0 years

4 - 4 Lacs

Bharuch

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* Instrument Handling of GC, HPLC, Karl Fischer, pH meter, Auto Titrator apparatus, Malvern Partial size analysis etc. * Good understanding of ISO 9001:2015 Quality Management System. * Hands of experience on SAP,COA & Analysis of COD sample. Required Candidate profile * Perform analysis of the raw materials, wet lab analysis, solution preparation, In-process sample. * Preparation of table top SOP’s and detailed manual on Start-up and Shut-down of the equipment

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0.0 - 3.0 years

2 - 2 Lacs

Dahej

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Role & responsibilities

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1.0 - 5.0 years

3 - 7 Lacs

Rajkot

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SHRI BHAGAVATI BRIGHT BARS LTD is looking for Quality Control Executive to join our dynamic team and embark on a rewarding career journey. Assist in quality control tasks and activities. Develop and implement quality control policies and procedures. Monitor and report on quality control performance metrics. Collaborate with quality control teams and stakeholders. Ensure compliance with quality control standards and regulations.

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2.0 - 5.0 years

4 - 6 Lacs

Pune

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Long Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

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0.0 - 4.0 years

2 - 5 Lacs

Ahmedabad

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Roles and 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. Desired 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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1 - 3 years

2 - 3 Lacs

Hyderabad

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Job Title: Junior Analyst / Analyst Experience: 1 to 3 years Location: Hyderabad CTC: 2.5 3.5 LPA Qualification: M.Sc. in Chemistry / Analytical Chemistry Preferred profile: from a food testing laboratory background Job Description: We are seeking a dedicated and skilled chemist with 1 to 3 years of experience in HPLC impurity analysis handling within the food testing industry. The ideal candidate should have a strong foundation in analytical chemistry, method development, and instrument calibration. Key Responsibilities: Perform HPLC impurity analysis in accordance with regulatory and laboratory standards. Conduct routine calibration and maintenance of HPLC instruments. Ensure accurate documentation of sample preparation, analysis, and results. Adhere to Good Laboratory Practices (GLP), ISO 17025 standards, and safety protocols. Assist in method development and validation as per standard operating procedures. Maintain and update instrument logs and calibration records to support audit readiness. Collaborate with QA/QC teams to ensure compliance and continuous improvement. To analyze all Food & Agri samples using HPLC as per IS, AOAC, FSSAI , SOP and customer supplied methods. To Calibrate and perform Intermediate checks for all major and minor laboratory instruments such as HPLC, pH meter, micropipette, sonicator etc. To analyze all the food & Agri samples using GC and UV-Visible spectrophotometer as per IS, AOAC, FSSAI and customer supplied methods. To develop, validate and verify methods as per requirement using HPLC & GC. Candidate Requirements: M. Sc - Chemistry. 1 to 3 years of relevant experience in HPLC and GC techniques, preferably in a food testing laboratory. Hands-on experience with chromatographic software and analytical instrumentation. Willingness to work in rotational shifts. Flexibility to relocate to other branches across India including Bangalore, Nellore, Nashik, Mumbai, Ahmedabad, and Noida for deputation or transfers. Strong analytical skills, attention to detail, and effective communication abilities. Regards, Priyanka Jajula Sr. Executive - HR

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3 - 8 years

4 - 6 Lacs

Mundra

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Role & responsibilities Inspects tests, adjusts, and repairs electric, electronic, mechanical, and pneumatic instruments and systems used to indicate, record, and control generating operations in conventional process plant: Inspects meters, indicators, and gauges to detect abnormal fluctuations. Tests accuracy of flow meters, pressure gauges, temperature indicators, controllers or detectors, and other recording, indicating or controlling instruments to locate defective components in system, using test equipment, such as pressure gauges, mercury manometers, potentiometers, pulses, load cell, PID Controller, PH Meter, Level Gauge & Level Transmitter. Prepares schematic drawings, sketches, and reports to reflect changes or alterations made in instruments, circuits, and systems. disassembles, and cleans instruments, and replaces defective parts, using hand tools. Reassembles instruments and replaces instruments in system, using hand tools. Lubricates instruments and replaces defective wiring and tubing. Calibrates readings on instruments according to standards and adjusts phasing and aligns stages to ensure accuracy of recording and indicating function. Records calibrations made, parts and components used, and inventory of parts on hand. Responsible for EHS & RC Related compliance. May be designated according to type power plant as Process-Plant-Instrument Technician, Instrument Repairer, Boiler Plant. Removes defective instruments from system, decontaminates, Preferred candidate profile Working knowledge Emerson / Yokogawa DCS, Programable Logic Controller based chemical manufacturing plant. Technical knowledge of field instruments like flow meter, flow switches, control valves etc.

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3 - 8 years

4 - 5 Lacs

Chiplun

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Laxmi Organic Industries Limited. We are looking for candidates interested in Technical Associate-Quality for Chiplun. Job Title: Technical Associate-Quality Department: Quality Control/ Quality Assurance Location: Lote, Chiplun. Job Purpose Analysis of Raw material, water sample, Packing material In-process & Finished products Role and Responsibilities Operational: Daily analysis of water, In-process, Daily Finished product sampling and analysis Daily sampling of RM, In-process, Finished product. Dispatch of finished product dispatches of tanker, drum, bags sampling and analysis. Counter samples storage, retrieval, instruments cleaning Detection of abnormalities during analysis and report it to the concerned authority. Raw Material inspection, sampling and analysis. Result recording in SAP. HPLC and GC Data storage Packing material sampling and analysis. Checking of certificate of analysis Report any near miss /incident or any non-compliance To Support Various ISO, Process safety and Responsible Care Initiatives Responsible to compete any other assignment given by the senior. Deviation reporting and recording OOS reporting and recording. Required Knowledge (of any equipment / Tools and techniques / Software) GC, HPLC, UV, Titrimetric, Karl Fischer, Potentiometer, QESH Education Essential: M.Sc in Chemistry Preferred: M.Sc in Chemistry (Analytical, Organic, Inorganic) Experience Essential: 2-4 years in chemical industry Preferred: Experience in Pharmaceutical Industry If you are interested, kindly share your updated cv on below email id. Email Id: viddhi.kharwa@laxmi.com Telephone No: 91-22-4910444-ext.513

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2 - 4 years

1 - 4 Lacs

Bengaluru

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Role & responsibilities Preferred candidate profile Perks and benefits

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5 - 9 years

7 - 9 Lacs

Ankleshwar, Panoli

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Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

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- 5 years

3 - 5 Lacs

Hyderabad/ Secunderabad

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Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. Department: Pharma Standard - Quality Control Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Theoretical knowledge and hands-on experience on instruments like Shimadzu HPLC with Lab solution software, Agilent HPLC, Balance, pH meter, TGA instrument, FTIR. CGMP,GMP, experience on LCMS is preferrable. Knowledge on Data Integrity, GDP, QMS. Department: Pharma Standard - Inventory Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Management of Inventory items, handling, weighing, dispatching of inventory materials. Hands-on experience on semi-microbalance, microbalance. Maintaining Real time stock updation of the inventory list in excel or SAP system and updating the stock quantities to the relevant stakeholders, whenever required. Basic understanding on Data Integrity, GDP and QMS Please bring your Updated CV along with last 3 Months Payslips, Recent Increment Letter, Aadhar Card/PAN Card: Date : Saturday, 10 May 2025 Time: 09:00 AM to 4:00 PM Walk-in Interview Location: Daicel Chiral Technologies (India) Pvt Ltd Genme Valley, IKP Knowledge Park, Survey No. 542/2, Koltur Village, Shamirpet Mandal, Medchal-Malkajgiri District, Hyderabad-500101 Note: Candidates who are unable to walk-In, May send their resume to hr@chiral.daice.com or whatsApp to 9000066897

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- 5 years

3 - 5 Lacs

Hyderabad/ Secunderabad

Work from Office

Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. ************************************************************************************************** Department: Pharma Standard - Quality Control Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Theoretical knowledge and hands-on experience on instruments like Shimadzu HPLC with Lab solution software, Agilent HPLC, Balance, pH meter, TGA instrument, FTIR. CGMP,GMP, experience on LCMS is preferrable. Knowledge on Data Integrity, GDP, QMS. ************************************************************************************************** Department: Pharma Standard - Inventory Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Management of Inventory items, handling, weighing, dispatching of inventory materials. Hands-on experience on semi-microbalance, microbalance. Maintaining Real time stock updation of the inventory list in excel or SAP system and updating the stock quantities to the relevant stakeholders, whenever required. Basic understanding on Data Integrity, GDP and QMS Please bring your Updated CV along with last 3 Months Payslips, Recent Increment Letter, Aadhar Card/PAN Card: Date : Saturday, 10 May 2025 Time: 09:00 AM to 4:00 PM Walk-in Interview Location: Daicel Chiral Technologies (India) Pvt Ltd Genme Valley, IKP Knowledge Park, Survey No. 542/2, Koltur Village, Shamirpet Mandal, Medchal-Malkajgiri District, Hyderabad-500101 Note: Candidates who are unable to walk-In, May send their resume to hr@chiral.daice.com or whatsApp to 9000066897

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2 - 6 years

2 - 5 Lacs

Bharuch, Dahej

Work from Office

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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5 - 9 years

3 - 4 Lacs

Ankleshwar, Panoli

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Position: QC Officer Qualification: B.Sc / M.Sc in Chemistry Experience: 3 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 4.5 Lacs per Annum. Location: Ankleshwar / Panoli. It's a Shift Working job Transport Provided. Industry: API PHARMA ONLY Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

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5 - 9 years

5 - 6 Lacs

Ankleshwar, Panoli

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Position: QC Executive Qualification: B.Sc / M.Sc in Chemistry Experience: 5 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 6.5 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API / Bulk Drugs / Pharma. Those working in Crop Sciences, Fertilisers are not eligible. Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

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2 - 7 years

1 - 3 Lacs

Palghar

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Perform sampling and testing of raw materials, packaging, and finished products. Maintain QC records and documentation as per SOPs. Ensure compliance with GMP, ISO, and regulatory standards. Report quality issues and support corrective actions. Required Candidate profile B.Sc./M.Sc. in Chemistry 2+ years in Quality Control, preferably in cosmetic or chemical ind Know of analytical instruments Strong attention to detail and understanding of quality standards.

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1.0 - 4.0 years

1 - 4 Lacs

parner

Work from Office

Responsibilities: * Conduct quality control tests using GC, Karl Fischer, pH meter, bom & density measurements * Ensure compliance with industry standards and customer requirements Health insurance Provident fund

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2.0 - 5.0 years

3 - 4 Lacs

vapi

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Role & responsibilities : 1) To plan analysis of in- process, intermediate, raw material, stability sample, holding time study sample & finished products on HPLC & check report of the same. (Dirty Equipment & Clean Equipment) 2) To distribute the shift wise work to analyst as per requirement in HPLC section & To plan calibration of HPLC /analytical balance as per schedule and review the same.

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1.0 - 3.0 years

2 - 3 Lacs

bharuch, ankleshwar

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Supervise & monitor daily operations of the ETP including primary, secondary & tertiary treatment process Ensure compliance with statutory environmental norms & effluent discharge standards Train & guide operators for safe & efficient plant operation Required Candidate profile Coordinate with the EHS department for sampling, testing & record-keeping of treated water Operate & maintain pumps, blowers, dosing systems, filters & other ETP equipment Ensure safety compliance

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0.0 - 2.0 years

0 - 2 Lacs

bengaluru

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

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0.0 - 4.0 years

2 - 5 Lacs

dahej, ankleshwar

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Skills : HPLC , GC, KARL Fisher, pH Meter, Education : MSC (chemistry) Ctc : 5.5LPA Location : Dahej/ Ankleshwar Prefreed candidates from ETP/ STP/ WTP industry.

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4.0 - 8.0 years

8 - 14 Lacs

bengaluru

Hybrid

Role & responsibilities To handle all assigned VAR's independently and Make them viable for LAB BA, ALL Segment business through VAR (Channel). Value Selling (To Position product & sales Low / Mid/High Value Equipment's). To generate Sales thru Lab equipment VAR's,Sub-dealers, agents-from the Industry Segments (Pharma, Chemical, Food, Education, Govt Research Institutes etc) and convert the same in to Sales Order. Build techno/commercial competencies in the channels. Develop and implement stock and sale strategy . Support VAR for Lead. Monitor Leads on regular basis. Manage channel sales directly and indirectly working with Dealers. To coordinate with dealer and MT for smooth business. Achieve monthly/Quarterly/Yearly business targets as per the dashboard. VAR (Channel) Deployment (as per business demand) & VAR Development. Partner with all stakeholders in a matrix organization for the business success. Preferred candidate profile M.Sc. / B.Sc. / Degree / Diploma in Engineering. (Chemical / Electronics / Instrumentation), MBA-Sales & Marketing. Experience in selling Equipment's, Instruments or equivalent. Dealer management Experience will be preferred Interested Applicants can forward resume on Carol.rodrigues@mt.com

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2.0 - 7.0 years

1 - 3 Lacs

palghar

Work from Office

Perform sampling and testing of raw materials, packaging, and finished products. Maintain QC records and documentation as per SOPs. Ensure compliance with GMP, ISO, and regulatory standards. Report quality issues and support corrective actions. Required Candidate profile B.Sc./M.Sc. in Chemistry 2+ years in Quality Control, preferably in cosmetic or chemical ind Know of analytical instruments Strong attention to detail and understanding of quality standards.

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8.0 - 10.0 years

8 - 10 Lacs

dahej

Work from Office

Oversees QC processes, ensuring products meet specified std. Developing and implementing QC procedures, conducting audits, and resolving qc-related issues. trains the QC team, maintains records, and ensures compliance with regulatory standards

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