290 Spectrophotometer Jobs - Page 8

We are seeking a highly skilled Lab Chemist to join our team. The ideal candidate will be responsible for conducting chemical analyses, ensuring quality control, and supporting research and development activities in our water and wastewater treatment processes. Job Location: ION TECHNIQUES, F2, SIDCO Industrial Estate, Dindigul, Tamil Nadu 624003 Key Responsibilities: Perform chemical and physical testing on water and wastewater samples. Operate and maintain analytical instruments (e.g., pH meter, spectrophotometer, titration, COD/BOD analyzers). Ensure compliance with environmental regulations and industry standards . Develop and implement quality control procedures for chemical analysis. Prepare and maintain detailed laboratory records and reports . Collaborate with engineers and plant operators to optimize treatment processes . Ensure safe handling and disposal of chemicals following lab safety protocols. Conduct research and testing for new treatment chemicals and technologies . Qualifications & Requirements: Bachelor’s/Master’s degree in Chemistry, Environmental Science, or related field . 1-5 years of experience in a laboratory setting (preferably in water/wastewater treatment). Strong knowledge of chemical analysis methods and instrumentation . Familiarity with ISO, EPA, and ASTM standards is a plus. Excellent analytical, problem-solving, and documentation skills. Ability to work independently and as part of a team. Interested candidates are invited to submit their resume and walk in interview ION TECHNIQUES, F2, SIDCO Industrial Estate, Dindigul, Tamil Nadu 624003 Balaji 8610929261 Job Type: Permanent Pay: ₹10,000.00 - ₹25,000.00 per month Benefits: Cell phone reimbursement Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Title: Senior Officer - ADL Custom Field 2: 2559 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. 2) Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. 3) Preparation and maintenance of volumetric solutions, buffers, etc 4) Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., as per calibration schedule 5) Knowledge of separation techniques in chemical separation in chromatography in Normal and reversed phase systems 6) Experience in chemical analysis like, titration, moisture, LOD, sulphated ash, TLC IR, SOR, Clarity of solutions and quantitative solubility tests 7) Exposure of GMP / GLP / GDP in laboratory. 8) Preparation of Standard operating procedures (SOP) for all the instruments, equipment and procedures. Job Segment: Chemical Research, Laboratory, Engineering, Science

Title: Officer Custom Field 2: 2216 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. Preparation and maintenance of volumetric solutions, buffers, etc Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., as per calibration schedule Job Segment: Laboratory, Science

Job Profile : A Quality Control Officer is a professional who is Responsible for the Raw materials. in process and finished product and also stablility samples analysis and had knowledge of handling instruments like HPLC , UV-visible spectrophotometer , Dissolution Apparatus, pH meter , viscometer , KF, Polarimeter , Refractometer, Friabilator, D.T. Apparatus etc. Roles & Responsibilities: Responsible for inprocess and finished product analysis and also analysis of stability samples. Handling instrument like HPLC, UV-visible spectrophotometer, Dissolution Apparatus, pH meter, KF, Polarimeter, Refractometer, Friabilator, D.T. Apparatus etc. Analysis of finished product, stability product and raw material. Preparation of SOP for related to instrument and system. Preparation of protocol, worksheet for raw material and finish product. Documentation Validation protocol, Validation report, STP preparation. Performing sample based check, monitor transactions & provide feedback on quality. Sampling of Raw material, entry, packaging and labeling. Supporting completion of audit checklist in advance for all internal/ external audits. Assisting company's external auditors for preparation of documentation for control weakness/ error remediation. Standardization and Calibration of Instruments. Water analysis. Perform other duties as assigned. Candidate Profile / Skill required : Knowledge of GMP & GLP,ICH guidelines. Working knowledge of Analytical Method development and validation. Handling of instruments like HPLC/Spectrophotometer etc. In-depth understanding of company standards Up-to-date knowledge of federal and industry standards and best practices Basic computer and math skills to calibrate and measure specifications A keen eye for detail Good verbal and written Communication skills Proficiency in Microsoft Office Knowledge of pharmasuite/pharmacloud software. Required Qualifications : M.SC.,B.Pharm,M.Pharm A minimum of 1-2 years related experience in QC pharmaceutical manufacturing company.

We are seeking a highly skilled Lab Chemist to join our team. The ideal candidate will be responsible for conducting chemical analyses, ensuring quality control, and supporting research and development activities in our water and wastewater treatment processes. Key Responsibilities: Perform chemical and physical testing on water and wastewater samples. Operate and maintain analytical instruments (e.g., pH meter, spectrophotometer, titration, COD/BOD analyzers). Ensure compliance with environmental regulations and industry standards . Develop and implement quality control procedures for chemical analysis. Prepare and maintain detailed laboratory records and reports . Collaborate with engineers and plant operators to optimize treatment processes . Ensure safe handling and disposal of chemicals following lab safety protocols. Conduct research and testing for new treatment chemicals and technologies . Qualifications & Requirements: Bachelor’s/Master’s degree in Chemistry, Environmental Science, or related field . 1-5 years of experience in a laboratory setting (preferably in water/wastewater treatment). Strong knowledge of chemical analysis methods and instrumentation . Familiarity with ISO, EPA, and ASTM standards is a plus. Excellent analytical, problem-solving, and documentation skills. Ability to work independently and as part of a team. Interested candidates are invited to submit their resume and walk in interview ION TECHNIQUES, F2, SIDCO Industrial Estate, Dindigul, Tamil Nadu 624003 ARUN - HR, 8438391401 Job Type: Permanent Pay: ₹10,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Position: Laboratory chemist (Pharmaceutical Industry) Experience: 1 to 2 Years Education: MSC/ B.pharma/ M.pharma Location: Kalol, Ahmedabad Preferred Location: Kadi, Kalol, Gandhinagar, Mehsana Job Summary: We are seeking a dedicated and detail-oriented Laboratory Chemist to join our Quality Control team in the pharmaceutical manufacturing sector. The ideal candidate will have hands-on experience with analytical techniques and instruments used in QC labs and will ensure that all pharmaceutical products meet stringent quality standards. Key Responsibilities: Perform chemical and physical analysis of raw materials, in-process samples, and finished products. Operate and maintain laboratory instruments such as HPLC, UV-Vis spectrophotometer, IR spectrometer, pH meter, and others. Conduct stability studies and document results as per regulatory requirements. Prepare and standardize volumetric solutions, reagents, and buffers. Maintain proper documentation (raw data, logbooks, reports, etc.) in compliance with cGMP, GLP, and regulatory guidelines. Participate in internal audits and assist in addressing non-conformances. Calibrate instruments and maintain calibration records as per the schedule. Follow Standard Operating Procedures (SOPs) strictly to ensure accuracy and reliability of results. Coordinate with the production and QA departments for sample collection and result reporting. Qualifications: B.Sc. / M.Sc. in Chemistry, Pharmaceutical Sciences, or related field. 1–2 years of experience working in a pharmaceutical Quality Control laboratory. Familiarity with regulatory standards such as WHO-GMP, cGMP, ICH guidelines. Proficiency in analytical techniques and understanding of pharmacopeial methods (IP/BP/USP/EP). Good documentation practices and attention to detail. Ability to work independently as well as in a team environment. Preference: Local candidates will be given preference, especially those residing in or near Kadi, Kalol, Gandhinagar, or Mehsana . Job Type: Full-time Pay: ₹18,000.00 - ₹25,000.00 per month Schedule: Day shift Work Location: In person

Company Description Shrestha Bio Organics produces premium-grade, organic-certified vermicompost. Key Responsibilities: Lab Operations & Supervision: Lead the day-to-day lab testing of raw materials, compost, and finished vermicompost products. Supervise junior lab technicians and ensure proper laboratory practices. Maintain and calibrate laboratory instruments regularly. 2 Quality Control & Assurance: Perform quality testing for parameters such as moisture content, pH, C:N ratio, NPK levels, microbial count, and heavy metals. Ensure the final product meets FCO (Fertilizer Control Order) and organic certification norms. Maintain detailed logs and reports of analysis. 3 Documentation & Reporting: Prepare daily/weekly/monthly test reports. Maintain lab records as per ISO/organic certification or internal standards. Report any deviation or non-conformance in materials to management. 4 Process Improvement: Suggest improvements in composting process based on lab results. Participate in R&D projects related to microbial inoculants, organic additives, or new formulations. 5 Compliance & Safety: Ensure lab compliance with safety, health, and environmental regulations. Maintain safe handling and disposal of chemical reagents and biological samples. Key Skills Strong understanding of composting biology, organic fertilizers, and soil science. Hands-on experience with lab equipment like pH meter, spectrophotometer, moisture analyzer, etc. Analytical mindset and attention to detail. Team leadership and training capabilities. Good computer and documentation skills (Excel, Word, Lab software). Qualifications: B.Sc. / M.Sc. in Chemistry, Agriculture, Environmental Science, or related field. 8+ years of lab experience in compost/ soil scienc e. sector. call us on 9845395875

Responsibilities: * Conduct analytical tests using HPLC, GC, Karl Fischer, spectrophotometer, pH meter, Karl Fischer titrator, viscometer, autotitrator & melting point apparatus.

Location: Talaja Plant, Gujarat Company: Shubham Nutri Foods Email for resume submission: snf@shubhamnutrifoods.com Position Summary: The Quality Control Executive will be responsible for maintaining and monitoring product and process quality at every stage of production—from raw material intake to finished product shipment. The candidate must ensure that all quality systems align with global food safety standards, as the entire business is export-oriented. Key Responsibilities: Conduct regular quality checks and lab testing for raw peanuts, roasted peanuts, peanut paste, and finished peanut butter. Monitor critical control points (CCPs) in production and report deviations promptly. Ensure adherence to BRC, USFDA, ISO 22000, Kosher, and Halal guidelines throughout production. Supervise hygienic practices on the shop floor, including GMP (Good Manufacturing Practices) and GHP (Good Hygiene Practices). Coordinate with production, maintenance, and packaging teams to implement corrective and preventive actions (CAPA). Perform sensory evaluation (taste, texture, aroma) and physical inspection of products. Maintain and review quality records including COAs, batch reports, traceability records, and lab test results. Handle customer complaints, non-conformities, and audits (internal & external). Liaise with third-party labs for periodic testing (aflatoxin, microbiological, pesticide, heavy metals, etc.). Support new product development trials and shelf-life studies. Train factory staff on quality protocols and food safety awareness. Key Skills & Qualifications: B.Sc./M.Sc. in Food Technology, Microbiology, or related field. 2–5 years of QC experience in the food processing or peanut butter/edible oil industry. Sound knowledge of export documentation and international food safety norms. Experience working in BRC-certified environments is highly preferred. Familiarity with lab instruments (Moisture Meter, pH Meter, Spectrophotometer, etc.). Strong documentation, report writing, and MS Office skills. Detail-oriented, with analytical thinking and problem-solving mindset. Good communication and coordination skills for internal and external audits. What We Offer: Opportunity to work with a fast-growing export-focused brand. Professional development and learning environment. Competitive compensation aligned with industry standards. Chance to be part of a passionate and committed quality-driven team. 📧 To apply, please email your CV to: snf@shubhamnutrifoods.com 🕒 Only shortlisted candidates will be contacted.

Role & responsibilities 1.HPLC,UPLC and GC analysis of raw material, intermediate, finish product, stability sample, equipment cleaning and distilled solvent, Analytical Method development and validation 2.HPLC,GC, UPLC calibration HPLC and GC Analysis of all in-process,Intermediate, Finish Product,Stabiltity Analysis Equipment cleaning, Distilled Solvent and Raw materials. If required then sampling of finished product. Working Standard Qualification. Calibration of HPLC and GC. GCHS. R&D Analytical Metliod Development of new molecule. Analytical Method Validation. lnstnmrent Troubleshooting

Senior QC/Quality Control Executive Formulation Pharmaceutical Having exposure to instrumentation: Spectrophotometer, Karl Fischer- auto titer

http://nauk.in/bpfLwvP Key Responsibilities: Perform analysis of raw materials, intermediates, and finished products of Active Pharmaceutical Ingredients (APIs) as per approved specifications and SOPs. Operate and maintain analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, Melting Point Apparatus, etc. Review and verify analytical data and ensure proper documentation in line with cGMP and GLP guidelines. Prepare and standardize volumetric solutions and reagents. Carry out stability studies and maintain stability data as per ICH guidelines. Ensure timely calibration of laboratory instruments. Perform method validation/transfer activities as per regulatory and internal requirements. Involve in investigations related to OOS/OOT/Deviations and CAPA implementation. Coordinate with cross-functional departments like QA, Production, and R&D for smooth workflow. Comply with all safety protocols and maintain a clean and organized lab environment. Desired Candidate Profile: Hands-on experience in analytical techniques (HPLC/GC) is a must. Good knowledge of regulatory guidelines (ICH, WHO, USFDA, etc.) Strong documentation and communication skills. Experience in a regulated API manufacturing unit is preferred. Industry Type: Pharmaceutical & Life Sciences Department: Corporate Quality Control Employment Type: Full Time, Permanent

The Opportunity Under close supervision, provide availability of refub instruments, troubleshooting, repairs and calibration to instruments; HPLC, GC, Spectrophotometer, electronic and mechanical equipment. Document and report all repairs and product failures, spare parts management. What We’re Looking For Education: Degree / Diploma in Electrical / Electronics / Biomedical engineering or any other stream Experience: Min 2-3 years of experience in Service in IVD How You Will Thrive And Create An Impact Service Center Activities Overall management of the Service Center ii) Receive and Log customer calls through Call Center Operation iii) Sharing the information with the in-house engineer to take the call forward iv) Managing Customer Data Base – Share Point Application Updating database Updating / Correcting any mis information in the Share Point / Power App Co-ordinate with warehouse for transfer of instruments to the Service Center & back for repairing / refurbishing / evaluation vi) Co-ordinate with Facility Team, for packing the instruments received at the Service Center (Need Based) vii) Maintaining Service Inventory of essential Spares & doing reconciliation monthly Engineering Activities Spares request from field engineers to be forwarded for processing further ii) Follow up with field engineers for the return of the defective / unused spares Admin Activities Preparing quotes for AMC / Spares and facilitate invoicing after realization of payments ii) Co-ordinate with internal teams (finance / facility / logistics / any other relevant…) to clear any bottle necks in the process iii) Create SAP codes, in the SAP system, for the spares which are not already in the system iv) Proactively analyze the spares consumption pattern and set up multi-level alerts to initiate re-ordering in consultation with the Head – Service & Application Ensure accurate records of all the service relates activities in the service center & from the field viz., Maintaining Installation Reports Maintaining PM Reports Maintaining any other service call records Communication / Coordination with Principal companies for, Escalation of technical calls from the field ii) Timely submission of warranty claims for the defective spares, from the field iii) Follow up for the submitted Warranty claims iv) Procurement of Spares / consumables quote Requirements Good communication skills Proficiency in writing Emails / working on excel Working knowledge on SAP would be an added advantage Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd Party Non-solicitation Policy By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation

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.