165 Spectrophotometer Jobs - Page 4

Job Description for the Post of Executive Quality Control Lab Location: Thirumudivakkam, Chennai 1. Job Responsibilities & Duties: a. Sampling from production areas for critical Processes. b. Executing production samples in the quality lab and preparing reports as per the required timelines of production. c. Planning for daily samplings and analysis. d. Handling of analytical instruments including HPLC, spectrophotometer, pH, TDS, viscometer, COD etc. e. Developing SOPs for new & corrective methods to simplify the critical analysis areas in production. f. Collaborating with the marketing team to do assessment of the customer complaints and troubleshooting of the product issues. g. Maintain quality standards by approving incoming materials, in-process production, finished products, and recording the results h. Knowledge on wet and dry analysis i. Support and manage the department budget in partnership with the Quality Manager j. Able to analyse quality data and drive Root Cause Corrective Actions (RCCA) k. Should be familiar with ISO audit process and control documents l. Familiarity with MS-Office tools such as Excel, Word, Power Point m. Maintain laboratory equipment and supplies as required n. Conducts testing of raw materials, intermediates, final products, or stability samples.Must be self-driven, results-oriented with a positive outlook and have a clear focus on quality Job requirements: A successful candidate will have: a. A profound knowledge of wet and dry analysis methods, saponification, chloride content, Hardness, Acid value, Solid content, handling of analytical instruments including HPLC, spectrophotometer, pH, TDS, Viscometer, COD etc. b. Aware with analytical skills including titration, preparation of standard solutions, standard calibration methods, etc. c. A masters degree in chemistry or Biochemistry from an accredited college/university and minimum 3+ years of experience in quality control lab. d. An inquiring mind, intense curiosity, and strong desire to work in quality method development. e. Good teamwork skills in fast faced & challenging environment. f. A sincere attitude & commitment towards job responsibilities. ***** Interested Candidates can share their profile to raksha@proklean.in *****

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-28-06-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, 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.

Interested candidates, kindly mail to enpcareers.hr@ril.com Main Purpose: Chemist Field Operations is responsible for sample collection, preservation, and laboratory analysis of natural gas, water, and specialty chemicals. Ensures compliance with international standards, equipment calibration, and QA/QC implementation. Manages lab inventory, documentation, and regulatory audits while generating detailed reports. Job Accountabilities: Collect, label, and log samples from production facilities, wells, pipelines, and storage tanks while ensuring proper storage and transport to maintain sample integrity. Conduct composition analysis of natural gas (methane, ethane, propane, BTU value, H₂S, CO₂, O₂) and water quality testing(pH, salinity, contaminants) for produced, utility, injection water, and effluents. Perform specialty chemical analysis, report preparation, and polymer analysis in produced well water to optimize chemical treatment processes. Maintain laboratory readiness for NABL accreditation audits, develop and update SOPs/SMPs for equipment and activities, and implement QA/QC systems. Ensure precise calibration of laboratory instruments, verify analytical methodologies, and uphold adherence to ASTM, API, and ISO standards. Track procurement of chemicals, maintain stock records of reagents, spares, consumables, and specialty chemicals, ensuring availability for uninterrupted lab operations. Archive lab data to meet NABL and regulatory audit requirements, maintain records for compliance, and ensure proper documentation of lab activities. Implement safety protocols for handling chemicals, follow environmental compliance standards, and ensure proper disposal of lab waste. Conduct mud analysis and prepare acid treatment plans for wellsite applications to enhance operational efficiency. Generate detailed laboratory reports, analyse data, and provide insights for process optimization, quality control, and regulatory submissions. Skills Required: Expertise in sample collection, gas and water testing, chemical analysis, and adherence to ASTM, API, and ISO standards. Experience in NABL accreditation, QA/QC, equipment calibration, regulatory compliance, and inventory management. Strong analytical skills, report writing, safety awareness, problem-solving, and effective communication. Heavy Metal Mercury analysis in Natural gas Lab analysis of Foamer/defoamer ,Corrosion inhibitor, Si chemicals SAP knowledge for creating PR and PO of Chemicals and service tracking with vendor & Procurement team LIMs portal operating and data updating Regular calibration, validation, and maintenance of analytical equipment Training lab personnel and lab equipment testing techniques Use of spectrophotometer, gas chromatograph, Online gas analyzer operating & troubleshooting NABL accreditation documentation at site Experience of facing Lab specific audits (e.g. ISO14001:2015,OMS etc.). Experience and Qualifications: BE (Chemical) / M.Sc. (Chemistry) Minimum 3 years in working experience in upstream (E&P)Oil/Gas Interested candidates, kindly mail to enpcareers.hr@ril.com

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compliance and safety requirements. Review of laboratory data, instrument logbook and reports wherever applicable. Initiation of departmental CCR's and tracking the progress to execute the proposed changes through QMS system. Preparation of TAP (Transfer of Analytical Procedures) protocol and Report for various sites. Procuring respective samples and Impurities accordingly. Planning and executing the assigned TAP projects to various sites. Preparation, maintenance and archival of regulatory submission documentation like SOP, protocols, reports for method development and validation. Job Responsibilities Prepares working plan for assigned projects and provides timeline to Deputy Manager. Develops stability indicative analytical methods for drug substance and finished product Responsible for all activities in Analytical Development, including cGLP, documentation and implementation of departmental quality systems. Responsible for protocol preparation, planning, execution, review and report preparation of various analytical method validation parameters. Ensures analytical methods validation is conducted according to approved validation protocol in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Responsible for method verifications and publishing of analytical methods Maintenance and archival of analytical method validation documents. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. Raising Change control for various analytical activities (Method SOP and department SOPs)by QMS trackwise To prepare General, Operation and Calibration Standard Operating Procedures. Responsible for initiation, execution and completion of technology transfer and collaborative validation activities of analytical methods to and / or from other departments of Apotex wherever applicable. Responsible for technology transfer and Transfer of analytical procedures activity to support the supervisor. Communicating the requirements for the Leaders and within the team members for effective cGLP procedures and departmental quality systems to achieve all outcomes. With guidance of scientists, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. To participate in the mandatory trainings to execute the day to day job responsibilities. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Practice and up-gradation of knowledge with respect to cGMP. Performs all work in accordance with all established regulatory and compliance and safety requirements. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Work as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education A graduate/post graduate in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, spectrophotometer and dissolution apparatus, wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge on preparation and review of various documents like SOP's, Formats, Protocols, Reports, analytical data, investigation and deviation reports. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities Should possess troubleshooting knowledge on Instruments and analysis. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 3-4 years’ experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com. Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compliance and safety requirements. Review of laboratory data, instrument logbook and reports wherever applicable. Initiation of departmental CCR's and tracking the progress to execute the proposed changes through QMS system. Preparation of TAP (Transfer of Analytical Procedures) protocol and Report for various sites. Procuring respective samples and Impurities accordingly. Planning and executing the assigned TAP projects to various sites. Preparation, maintenance and archival of regulatory submission documentation like SOP, protocols, reports for method development and validation. Job Responsibilities Prepares working plan for assigned projects and provides timeline to Deputy Manager. Develops stability indicative analytical methods for drug substance and finished product Responsible for all activities in Analytical Development, including cGLP, documentation and implementation of departmental quality systems. Responsible for protocol preparation, planning, execution, review and report preparation of various analytical method validation parameters. Ensures analytical methods validation is conducted according to approved validation protocol in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Responsible for method verifications and publishing of analytical methods Maintenance and archival of analytical method validation documents. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. Raising Change control for various analytical activities (Method SOP and department SOPs)by QMS trackwise To prepare General, Operation and Calibration Standard Operating Procedures. Responsible for initiation, execution and completion of technology transfer and collaborative validation activities of analytical methods to and / or from other departments of Apotex wherever applicable. Responsible for technology transfer and Transfer of analytical procedures activity to support the supervisor. Communicating the requirements for the Leaders and within the team members for effective cGLP procedures and departmental quality systems to achieve all outcomes. With guidance of scientists, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. To participate in the mandatory trainings to execute the day to day job responsibilities. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Practice and up-gradation of knowledge with respect to cGMP. Performs all work in accordance with all established regulatory and compliance and safety requirements. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Work as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education A graduate/post graduate in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, spectrophotometer and dissolution apparatus, wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge on preparation and review of various documents like SOP's, Formats, Protocols, Reports, analytical data, investigation and deviation reports. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities Should possess troubleshooting knowledge on Instruments and analysis. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 3-4 years’ experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Shift: 9:30 am to 5:30 pm Benefits: Food provided, Company bus pickup and drop Job Profile and Responsibilities To analyze in-process samples for Semi-Finished Goods & Raw Materials as per the Standard specification. To operate instruments like Spectrophotometer for shade analysis of Dye samples and absorbance of Material. Co-ordinate with export team for outgoing reference and pre-shipment samples. Documentation as per the ISO Norms Knowledge regarding Leather and Textile Dyeing Candidate Profile B.Sc./ M.Sc. in Chemistry or Diploma in Leather Technology Age- 20 to 25 Years age. Gender- MALE Experience- Freshers to 3 years Notice Period- Immediate to 15 days Job Types: Full-time, Permanent, Fresher Pay: ₹225,000.00 - ₹350,000.00 per year Benefits: Commuter assistance Food provided Provident Fund Schedule: Day shift Morning shift Ability to commute/relocate: Taloja, Navi Mumbai, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Work Location: In person

Designation: Instrumentation Technician (R&D Laboratory) Positions : 1 Qualification : B.Sc or M.Sc Experience : Minimum 2+ years in Instrumentation (R&D) Location : Balanagar, Head Office Department : R&D Laboratory Job Description : Operate, calibrate, and maintain laboratory instrumentation equipment. Troubleshoot technical issues related to lab instruments. Ensure proper functioning of analytical instruments like HPLC, GC, UV Spectrophotometer, etc. Maintain equipment records and calibration logs. Assist scientists and lab technicians during experiments involving instruments. Follow all safety protocols while handling instruments. Job Types: Full-time, Permanent Pay: ₹13,000.00 - ₹18,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Sales & Marketing of various types of Water Quality Instruments like Spectrophotometer , BOD , COD , PH/Cond /DO/TDS Meters - Generating sales leads in respective territory - Cold calling for customer meetings - Follow- up , Negotiate and close sales Required Candidate profile * Good communication, presentation and negotiation skills. * Excellence in sales and marketing with a positive attitude and team playing ability. * Ability to work independently.

Division VTC Mfg - MMR Job posted on Jun 23, 2025 Employee Type P-P8-Probationer-HO Executive Experience range (Years) 1 year - 6 years Walk In Interview for Vaccine Technology Center @ Pune Venue: Radisson Blu Pune Hinjawadi 136/1, Near Mahindra International School, Phase1, Hinjawadi, Pune. T: +91 020 69528000, M: +91 7888013458 Date: - 29.06.2025 (Sunday) Timing: - 9:00 AM to 5:00 PM Ø Education: - Post-Graduate M.Sc. in Biochemistry, Biotechnology, Microbiology, Lifesciences. Ø Experience: - 1-6 years of hands-on experience in relevant field, preferred Vaccine/Biotech background. Vaccine Manufacturing (Cell Culture) Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels. Experience in handling Roller bottles, Cell stacks, TCF’s. Experience in working in GMP conditions / production department of viral vaccines. Preparation of SOP, BMR’s, Protocols related to cell culture / virus culture. Experience in virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Quality Control (Bacterial/Viral) Candidate should have good knowledge of Product testing techniques like : Biochemical, Chromatography, Electrophoresis, Immuno assay, Cell culture & Molecular techniques. Experience in handling HPLC, Dionex, UV-Spectrophotometer, Multimode plate reader and ELISA -Shall be well versed with Biochemical assays (Protein, O-acetyl) immuno-chemical assays and electrophoresis, -Knowledge in calibration and qualification of equipment and instruments. -To perform/ monitor activities in compliance with GMP/GLP/GDP and record keeping. -Experience in preparing SOPs, Specification, STPs and Study protocols -To prepare method validation protocol and execute method validation. -Experience in handling stability studies and maintaining records. -Role shall require to coordinate with engineering/ maintenance department or third party labs as and when required. -Should possess basic skills in MS-Office, LIMS & SAP -Analyst shall be well versed with cell based assays, Virus titration, RTPCR and immuno-chemical assays. ==Instrument knowledge on pH meter, Analytical balance, Karl Fischer, Real time PCR and ELISA ==Knowledge in calibration and qualification of equipment and instruments. ==Experience in handling QMS elements like OOS, OOT, change control and deviation are added advantage. ==To perform/Monitor activities in compliance with GMP/GLP. ==Experience in preparing SOPs, specification and study protocols ==To prepare protocol and execute method validation ==Experience in handling stability studies and maintaining Good documentation practice. ==Role shall require to coordinate with maintenance department or third party lab as and when required.

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compliance and safety requirements. Review of laboratory data, instrument logbook and reports wherever applicable. Initiation of departmental CCR's and tracking the progress to execute the proposed changes through QMS system. Preparation of TAP (Transfer of Analytical Procedures) protocol and Report for various sites. Procuring respective samples and Impurities accordingly. Planning and executing the assigned TAP projects to various sites. Preparation, maintenance and archival of regulatory submission documentation like SOP, protocols, reports for method development and validation. Job Responsibilities Prepares working plan for assigned projects and provides timeline to Manager. Develops stability indicative analytical methods for drug substance and finished product Responsible for all activities in Analytical Development, including cGLP, documentation and implementation of departmental quality systems. Applies AQbD approach to analytical method development where applicable. Responsible for protocol preparation, planning, execution, review and report preparation of various analytical method validation parameters. Ensures analytical methods validation is conducted according to approved validation protocols in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Responsible for method verifications and publishing of analytical methods. Maintenance and archival of analytical method validation documents. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. Raising Change control for various analytical activities (Method SOP and department SOPs) by QMS trackwise To prepare General, Operation and Calibration Standard Operating Procedures. Responsible for initiation, execution and completion of technology transfer and collaborative validation activities of analytical methods to and / or from other departments of Apotex wherever applicable. Responsible for technology transfer and Transfer of analytical procedures activity to support the supervisor. Communicating the requirements for the Leaders and within the team members for effective cGLP procedures and departmental quality systems to achieve all outcomes. With minimal guidance, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. To participate in the mandatory trainings to execute the day to day job responsibilities. Assist in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GLP. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Practice and up-gradation of knowledge with respect to cGMP. Performs all work in accordance with all established regulatory and compliance and safety requirements. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Performs the calibration of instruments in Analytical R&D and ensures the compliance as per cGLP requirements. Work as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education A graduate/post graduate in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, UV, IR spectrophotometer and dissolution apparatus, wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge on preparation and review of various documents like SOP's, Formats, Protocols, Reports, analytical data, investigation and deviation reports. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities Should possess troubleshooting knowledge on Instruments and analysis. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 4 years or PhD with 2 years’ experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com. Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compliance and safety requirements. Review of laboratory data, instrument logbook and reports wherever applicable. Initiation of departmental CCR's and tracking the progress to execute the proposed changes through QMS system. Preparation of TAP (Transfer of Analytical Procedures) protocol and Report for various sites. Procuring respective samples and Impurities accordingly. Planning and executing the assigned TAP projects to various sites. Preparation, maintenance and archival of regulatory submission documentation like SOP, protocols, reports for method development and validation. Job Responsibilities Prepares working plan for assigned projects and provides timeline to Manager. Develops stability indicative analytical methods for drug substance and finished product Responsible for all activities in Analytical Development, including cGLP, documentation and implementation of departmental quality systems. Applies AQbD approach to analytical method development where applicable. Responsible for protocol preparation, planning, execution, review and report preparation of various analytical method validation parameters. Ensures analytical methods validation is conducted according to approved validation protocols in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Responsible for method verifications and publishing of analytical methods. Maintenance and archival of analytical method validation documents. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. Raising Change control for various analytical activities (Method SOP and department SOPs) by QMS trackwise To prepare General, Operation and Calibration Standard Operating Procedures. Responsible for initiation, execution and completion of technology transfer and collaborative validation activities of analytical methods to and / or from other departments of Apotex wherever applicable. Responsible for technology transfer and Transfer of analytical procedures activity to support the supervisor. Communicating the requirements for the Leaders and within the team members for effective cGLP procedures and departmental quality systems to achieve all outcomes. With minimal guidance, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. To participate in the mandatory trainings to execute the day to day job responsibilities. Assist in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GLP. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Practice and up-gradation of knowledge with respect to cGMP. Performs all work in accordance with all established regulatory and compliance and safety requirements. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Performs the calibration of instruments in Analytical R&D and ensures the compliance as per cGLP requirements. Work as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education A graduate/post graduate in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, UV, IR spectrophotometer and dissolution apparatus, wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge on preparation and review of various documents like SOP's, Formats, Protocols, Reports, analytical data, investigation and deviation reports. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities Should possess troubleshooting knowledge on Instruments and analysis. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 4 years or PhD with 2 years’ experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Role & responsibilities Physicochemical characterization, Media preparation, Buffer preparation etc. Preferred candidate profile Experience in working in lab set up and good basic knowledge on physical/chemical techniques. Dilligent and accuracy driven.

WE ARE HIRING R&D + QC OFFICER We are looking for one experienced candidate who can handle both Research & Development (R&D) and Quality Control (QC) responsibilities in our Herbal Extraction Unit. Requirements: Develop and optimize herbal extraction processes Conduct quality testing (raw materials & finished extracts) Maintain lab records & documentation Ensure GMP, safety, and compliance Good working knowledge of HPLC and UV spectrophotometer is essential Contact Us On :- Official@zivishaherbal.com

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt. Ltd.! We're hiring a Quality Control Head for our client. Qualification: MSc in Chemistry, Biochemistry, or a related field Location: Vikarabad District, Telangana Experience: 5 to 8 Years Salary: 3.5 lakhs to 4 lakhs per annum Required: Male Note: Preferably with strong experience in the pharmaceutical or ethanol industry. Job Summary: We are seeking an experienced Quality Control Head to lead the QC team at our client's facility. The ideal candidate will have a strong background in analytical techniques, including Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC), and will be responsible for ensuring the highest standards of product quality and regulatory compliance. Responsibilities: Lead, manage, and mentor the Quality Control team. Develop, implement, and oversee all QC procedures and protocols. Supervise analytical testing using GC, HPLC, Spectrophotometer, and other advanced techniques. Ensure all processes and products comply with regulatory requirements and industry standards (e.g., ISO, GMP). Collaborate effectively with production teams to identify and resolve any quality-related issues. Develop and implement robust quality control measures to guarantee final product quality. Train and develop QC team members to enhance their skills and performance. Requirements: Minimum of 5 to 8 years of experience in a Quality Control role. Strong hands-on knowledge of analytical techniques, especially Gas Chromatography (GC) and HPLC. Proven experience with regulatory compliance (e.g., ISO, GMP). Excellent leadership, communication, and problem-solving skills. Proactive, detail-oriented, and able to work in a dynamic environment. (Interested candidates can share their CV to aradhana@hungrybird.in or reach us at 9959417171.) Please furnish the below-mentioned details; that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: RAMESH, QC HEAD, 6 YEARS, 30 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards Aradhana +91 9959417171

To conduct and document analytical method validation (AMV), method verification, and method transfer activities for raw materials, in-process samples, and finished pharmaceutical products in compliance with ICH Q2(R1) , GMP , and regulatory standards . Key Responsibilities Analytical Method Validation Perform validation of analytical methods as per ICH Q2(R1) guidelines for: Assay and related substances (HPLC, UV) Dissolution, content uniformity, residual solvents (GC) Identification and other physicochemical parameters Conduct validation parameters: specificity, accuracy, precision, linearity, robustness, LOD/LOQ, system suitability, etc. Document results in validation protocols and summary reports. Method Verification Verify compendial methods (IP/BP/USP/Ph.Eur.) for RM/FP/IP samples. Confirm suitability of method for intended use before routine application. Prepare method verification reports and submit for review/approval. Method Transfer Participate in analytical method transfer (AMT) from R&D or third-party units. Execute comparative testing for transferred methods and compile transfer protocols. Coordinate with sending/receiving sites for method harmonization and troubleshooting. Instrument Handling Operate and troubleshoot instruments such as: HPLC (Empower, LabSolutions, Chromeleon) GC (Headspace, FID) UV-Visible Spectrophotometer FTIR, Dissolution Apparatus, TOC (if applicable) Documentation & Compliance Prepare and review: Validation protocols and reports Analytical worksheets and system suitability documents Adhere to GMP, GLP, and ALCOA+ principles. Maintain instrument logs, change controls, and CAPA logs where applicable. Audit Readiness & Regulatory Support Ensure all AMV data is audit-ready and compliant with regulatory expectations. Support in regulatory inspections (USFDA, MHRA, WHO-GMP, etc.). Address audit observations related to analytical validation. Instruments & Software Used HPLC, GC (Headspace, FID) UV-Vis Spectrophotometer, FTIR Dissolution Testers CDS Software: Empower / LabSolutions / Chromeleon Education :M.Sc. (Analytical / Organic Chemistry) / M.Pharm

Post for QC Chemist in Pharma Formulation Unit - based at Vatva, Ahmedabad, Gujarat. Sections - Tab, Cap, Syp, Cream, Mouthwash, Dry Powder, SoftGels Required Work Experience - Testing of Finished Formulation, API & Excipients Testing on Instruments like HPLC, Spectrophotometer, Dissolution Test Apparatus, Karl Fischer, Potentiometer, Titration, PH Meter, Analytical Balance, Hot Air Oven, etc. Work Experience - Required of QC Lab of Pharma Formulation Unit or FDA Approved Drug Testing Labs of Public or Private Sectors. Candidates (Do not apply for this job post) - with work experience from Other sectors like API, Dyes & Chemicals, Water Purification, Cosmetics, etc. Job Types: Full-time, Part-time Benefits: Flexible schedule Paid sick time Schedule: Day shift Supplemental Pay: Overtime pay Education: Bachelor's (Required) Experience: Quality control of Formulation Testing: 3 years (Preferred) Work Location: In person

We are seeking experienced chemists to join a talented and highly motivated team, involved in the purification of organic compound. The responsibilities will include pursuing a diverse R & D Program. Candidates should have an M. Sc. Degree in Organic Chemistry and have some working experience in HPLC and spectrophotometer.

Were Hiring: Service Engineer – TechnoValue Solutions Pvt Ltd Location: Navi-Mumbai / Hyderabad | Full-Time | Experience: 1–3 Years (Freshers with strong technical background can also apply) TechnoValue Solutions Pvt Ltd is looking for a dynamic and technically skilled Service Engineer to support our pharma clients with the installation, servicing, and maintenance of high-end laboratory and pharmaceutical instruments. Key Responsibilities: Installation, calibration, and servicing of pharma lab instruments at client locations Provide preventive maintenance and on-call technical support Troubleshoot and resolve issues related to hardware/software Maintain service records and submit reports regularly Ensure timely and professional support to pharma clients Requirements: Diploma/Degree in Electronics & Telecommunication, Instrumentation, Physics, Electronics Experience in handling pharmaceutical/laboratory instruments is preferred Good communication and problem-solving skills Willingness to travel to pharma plants, labs, and client locations Experience with HPLC, GC, UV-VIS, Dissolution Tester, or similar equipment will be a plus. Interested candidates can share their resume at technohr@technovalue.in or 8879773091. Join us in delivering reliable service and precision support to the pharma industry!

Company: Strides Pharma Science Limited Department: Quality Control Profile: Executive Locations: Bangalore Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years Key skills: Analysis of Material / Product by referring current version of specification STP with relevant material code. Responsible for initial set up of Instrument/Equipment before starting the analysis with relevant online entries in usage Log / LIMS. Perform the Assay and RS by LC/UV/Dissolution, content uniformity by LC analysis with simple and complex products Tests as per SOP/STP. Proper handling of chromatographic column used for analysis. Maintain data integrity and appropriate traceability

Job Title : Analyst – Air/Water Location : Mohali Experience : 1 to 3 years Department : Environment Laboratory Employment Type : Full-Time Reporting To : Lab Incharge / Technical Manager About the Role : We are looking for an experienced and detail-oriented Analyst to join our Environment Laboratory team. The candidate must have prior experience in a NABL accredited lab with hands-on expertise in Air and Water analysis . Key Responsibilities : Conduct sampling and analysis of ambient air, stack emissions, drinking water, groundwater, and wastewater as per standard methods (e.g., APHA, BIS, CPCB guidelines). Operate and maintain laboratory instruments such as Spectrophotometer, BOD Incubator, COD Digester, pH Meter, and other relevant equipment. Ensure accuracy and reliability of test results with adherence to SOPs and quality protocols. Maintain proper documentation and records as per NABL ISO/IEC 17025 standards. Assist in calibration and validation of laboratory instruments. Follow safety practices and contribute to laboratory cleanliness and compliance. Coordinate with field staff for sample collection and support external audits/inspections. Desired Candidate Profile : B.Sc. / M.Sc. in Environmental Science, Chemistry, or related field 1–3 years of experience in Air/Water testing in a NABL accredited laboratory Familiarity with NABL documentation and audit requirements Proficiency in operating laboratory instruments Strong attention to detail and quality Good communication and teamwork skills Job Types: Full-time, Permanent Pay: ₹12,086.00 - ₹30,341.54 per month Schedule: Day shift Fixed shift Weekend availability Work Location: In person

Job Description 👇 1. Media preparation. 2. FSIP (Full Sterilization in process). 3. ESIP (Empty Sterilization in process). 4. Seed preparation. 5. Handling harvesting process. 6. Handling whole fermentation process (Monitoring/ observing fermenter during production batch). 7. Handling of autoclave for material preparation. Looking after autoclave setting & troubleshooting. 8. IPQC using microscope, spectrophotometer, pH meter. 9. Microscopy checks for all samples, seed, “0” hour media count. 10. Handling Centrifugation process/Operating. 11. Monitoring lyophilisation during lyophilisation cycle. 12. CP batch preparation. 13. Lyophilisation loading & unloading. 14. Filling TRF & sample handover to QC department for testing. 15. BMR filling. 16. DMRD media Blending & Preparation.

Job description :- Instrumental Analysis: Perform routine and stability analysis of raw materials, intermediates, and finished products using HPLC, UV-Vis Spectrophotometer, FTIR , etc. Operate and calibrate analytical instruments as per SOPs and regulatory guidelines. Troubleshoot HPLC and other lab equipment in coordination with service engineers when required. Documentation & Compliance: Prepare and maintain analytical reports, test data sheets, protocols, and logs as per GDP (Good Documentation Practices). Ensure all QC activities comply with cGMP, GLP, and other regulatory guidelines . Assist in investigation and documentation of OOS, OOT, and deviations . Sample Handling & Testing: Receive and analyze raw material, packaging material, in-process samples, and finished goods as per approved specifications. Maintain proper sample disposal records. SOP & Record Management: Review and update Standard Operating Procedures (SOPs), specifications, and analytical methods. Maintain laboratory notebooks, logbooks, equipment usage logs, and calibration records accurately. Equipment Handling & Calibration: Operate and maintain lab instruments including HPLC, Dissolution Test Apparatus, pH meter, Analytical Balance, etc. Conduct periodic calibration and qualification of instruments. Audit Readiness: Prepare and support internal and external audits (e.g., USFDA, WHO, MHRA). Maintain complete and audit-ready documentation at all times. Key Skills & Competencies: Hands-on experience in HPLC analysis and troubleshooting . Strong understanding of analytical chemistry, GMP, GLP , and ICH guidelines . Attention to detail, data integrity, and documentation accuracy. Good communication and team coordination skills. Proficiency in MS Office and LIMS (preferred). Qualifications: B.Pharm / M.Pharm / M.Sc / B.Sc (Chemistry or related field) Minimum 2–5 years of experience in QC in a regulated pharmaceutical environment . Additional Requirements: Willingness to work in shifts (if applicable). Sound knowledge of safety protocols and laboratory hygiene . Good analytical and problem-solving abilities. Familiarity with regulatory audits and compliance standards . Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Joining bonus Performance bonus Yearly bonus Work Location: In person Expected Start Date: 01/07/2025

Should able to perform and supervise following routine tests of general chemical nature:- To perform all tests on water i.e. pH, TDS, TSS, harnesses, alkalinity, BOD, COD etc. Pigment testing, Chemical Testing, application, analytical testing

Key Roles & responsibilities: A reputed Railway product manufacturer seek to hire an Operational Excellence Engineer within the Quality Assurance Team to participate in continuous improvement and efficiency projects, focusing on products, systems, operations and processes. Defines, designs, and implements process improvement as part of organizations Operational Excellence, supporting business in establishing "best practice". Responsible for the creating Quality assurance plans (QAPs) for Indian Railways, Inspection Test Plans (ITPs), Manufacturing Process Plans (MPP) Responsible for RDSO , RITES & Third Party inspection handling & documentations Responsible for the creating Quality documents (Both Export & Indian Market). Ensures integration and alignment both vertically and horizontally across organization, within areas of safety, quality, delivery, productivity, cost and process efficiency. Facilitate and coach improvement teams, establishes and maintain performance metrics to track program success. Lead in Lean health checks, apply Lean methodologies such as PDCA, and perform Lean program audits and streamlining processes. Implement standard work process/procedures, visual factory and error proofing mechanisms. Provide technical leadership on Operational Excellence/Lean systems and tools. Responsible for making SOPs and their implementations. Create, maintain and refine a Lean toolkit that can include 5S, Kaizen, quick change over, value stream mapping, mistake proofing and line balancing, Muda Walk, KANBAN, TEAMWOOD, SMED, POKA Yoke. Requirements: 1 to 3 years of exp. BE/BTech/Mtech in Mechanical/Industrial Engineering. Railways Industry experience with respect to inspection handling is preferred. Experience with Lean Manufacturing techniques, e.g. leading Kaizen events, Continuous improvement, Six Sigma, Process / Value stream mapping, FMEA, Fish Bone. Certified Six Sigma green belt will be preferred. Good understanding of industrial standards and risk management practices. Good technical capabilities, communication skills, teamwork abilities and initiative. Proficient in Microsoft Excel, Word, and PowerPoint

Company: Strides Pharma Science Limited Department: QA/QC Profile: Executive Locations: Alathur/Puducherry Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years