98 Spectrophotometer Jobs - Page 4

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

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

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

Job Title: Junior Chemist – Agrochemical Industry Location: [Insert Location] Department: Quality Control / R&D / Production Lab Reports To: QC Manager / Lab Head / Plant Manager Experience Required: 0–2 years Employment Type: Full-time Job Summary: We are seeking a detail-oriented and enthusiastic Junior Chemist to join our agrochemical division. The role involves supporting the quality control and formulation teams by performing chemical tests on raw materials, technicals, and finished formulations under supervision. The candidate will work with common lab instruments and follow industry regulations and SOPs. Key Responsibilities: Assist in the analysis of technicals, formulations (EC, SC, WP, WG, etc.), and raw materials as per standard methods. Perform routine tests such as pH, specific gravity, viscosity, emulsion/stability, active ingredient content . Operate basic instruments like UV-Vis spectrophotometer, Karl Fischer, GC, HPLC (training will be provided if needed). Prepare reagents, standardize solutions, and maintain lab records as per SOPs. Ensure all samples are labeled, tested, and recorded accurately. Help with stability studies and maintain sample retention records. Support senior chemists in method development, pilot trials, and new formulation evaluations. Adhere to GLP, safety norms, and environmental standards during lab work. Required Qualifications & Skills: Education: B.Sc. / M.Sc. in Chemistry, Agrochemical Science, Industrial Chemistry, or related discipline. Experience: 0–2 years (freshers with internships in QC/R&D labs welcome). Skills: Basic knowledge of agrochemical formulations and testing procedures. Familiarity with laboratory safety and chemical handling. Willingness to learn analytical instruments and quality control documentation. Good observation, teamwork, and communication skills. Growth Opportunity: Exposure to QA/QC, R&D, regulatory documentation, and formulation technology . Hands-on training with industry-standard equipment and advanced lab techniques. Opportunity to grow into roles such as QC Chemist, Formulation Chemist, or Regulatory Analyst. Agrochemical Product Types You’ll Work With: Herbicides, Insecticides, Fungicides Liquid and Solid Formulations (EC, SC, WP, WG, SL, etc.) Job Type: Full-time Pay: ₹9,866.11 - ₹20,000.00 per month Benefits: Health insurance Paid sick time Schedule: Day shift Fixed shift Supplemental Pay: Yearly bonus Work Location: In person

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job summary We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performing the PM. To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP. To attend the breakdown's and close notification or order of the instrument /equipment after the Completion of breakdown maintenance. To be a part of investigating the incidence related to instrument Responsible for the maintaining of required spares for all instruments in warehouse. To get the quotations for the required spares and services for the maintenance of the instruments. To generate the purchase requisitions for the required spares and services. To perform the PM in the given frequency within the given period. Adhering to the allotted shift schedule with right time. If any changes prior permission shall be taken from Group leader. Qualifications Educational qualification: An B.Tech. or any Degree in Instrumentation, Mechanical, Electronics, Electrical. Required Work experience: 3 to 6 years Skills & attributes: Technical Skills Hands-on Experience on maintenance of Waters HPLC (Arc, e2695), Agilent HPLC (1200, 1260 Infinity), Agilent GC-HSS (7890, 8890, 7897, G1888), Dissolution Testers (Electrolab, Sotax), Metrohm Titrators. Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). Basic knowledge in SAP usage Behavioural Skills Prioritizes effective communication and demonstrates a performance-oriented mind-set. Effective verbal and written communication skills. Performance-oriented approach, consistently striving for high standards. Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Quality Control Formulations For more details, please visit our career website at https://careers.drreddys.com/#!/

Mission As Quality Assurance Officer will be the responsible to ensure right quality of the products as per Stanley Stella standards by proper monitoring, inspecting & guiding before they reach to consumer. Your purpose will also be to implement the right SOP in each area which will help to preserve our reputation by ensuring that our product & services are capable to drive sustainable growth. Main responsibilities Yarn quality check. Printability check. Maintain Mini bulk file properly. Risky point analysis for any new styles & feedback to BLO PD and HQ before approval. Greige Fabric quality check & monitoring the Knitting parameter randomly. Recipe & process route check. Ensure Finished Fabric quality parameters with relevant fabric test reports as per quality manual. Approve finished fabric shade of each batch by visually & spectrophotometer. Check bulk Accessories on garments, trim cards. Cut panel check & keep record. Samples check before shipment at different stages of production and some special projects samples. Conduct PP Meeting Ensure all quality parameters from Cutting, Sewing, Finishing & Packing as per company’s technical information manual/standard. Be present at the production line set up /first product flow, for new styles. In-line inspection & Final inspection. Keep record from the washing plant for all the panel wash garments. Dealing with vendors on quality issues and give solutions. Packing accuracy check on a daily basis (Mixed boxes/Missing pcs/sticker info vs content, etc.). Production line status update to line manager on a daily basis and update the OT status in common portal. Daily follow up C.S.R point in the production floor & make a report (monthly) and send to line manager. ETP PH Test (weekly) & make report. Weekly update of the factory’s quality situation to line manager. Guide the supplier in STST expectations and requirements. Your profile Graduate/ Masters. Educational Background on Textile Technology will be added advantage for the positions 5years of relevant work experience, good product and production knowledge with inspection criteria, AQL, shade and defects type, etc Strong leadership skill and teamwork mentality Exposure in Quality Assurance Excellent communication both verbal and written, analytical and interpersonal skills Computer literacy is must, especially strong skill to work in Excel. Flexible on working hours, Ability to work under pressure Ability to work with smart technology i.e., Tablet/Laptop for various reporting About us Stanley/Stella is the European leader in premium, sustainable blank apparel. Over the past decade, we’ve built the strongest brand in our industry — driven by a deep sense of purpose and a clear vision for the future of fashion. As a global company with multiple entities worldwide, we operate with integrity and care at every level. Sustainability is embedded in every decision we make — from the way we design our products to the long-term partnerships we build across our supply chain. We hold ourselves accountable not only for what we create, but how we create it. Excellence is our standard — from product quality to customer experience. We are uncompromising when it comes to detail, consistency, and delivering on our promises. And as the world evolves, so do we. Innovation fuels our ambition, inspiring us to challenge the norm, explore new ideas, and keep moving forward. At Stanley/Stella, we’re not just shaping the future of responsible fashion — we’re doing it together, with intention and heart. Ready to be part of the journey? Learn more: careers | Stanley/Stella

To provide analytical support for the ongoing / new projects with respect to method development, method validation, method transfer, testing and troubleshooting, aligned and supporting to the organization objective by practicing the values and Play to Win behaviors. Responsible for preventing accidents, avoiding risks to health and prohibiting environmental damage. Responsible for respecting all the applicable laws and regulations and implement professional guidelines and use the best industrial practices This role at MSAT Global Development Center, Goa requires focus and commitment associated with the deliverables and add value for the internal customers. Essential job duties and responsibilities Qualify, operate, calibrate, and maintain analytical instruments like HPLC, FTIR, GC, UV Spectrophotometer, LC-MS, GC-MS, Dissolution test apparatus & other analytical equipments. Method Development for Small Molecules and Solid Oral Dosage Forms including other novel drug delivery systems and advanced dosage forms. Develop Chromatographic method development which can extended to LC -MS , GC-MS or on other high end techniques for Genotoxic Impurities. Develop stability indicating methods for estimation of actives from DS & DPs. Dissolution method development and correlation to in vivo studies. Validation of analytical procedures in line with global guidelines. Impurity profiling & Characterization for Unknown Impurities. Analyze development samples and stability samples of the drug product. Perform stability studies as per EU/ICH guidelines. Perform analytical method transfer from development lab to QC lab in Manufacturing premises. Author complex documentation, including SOPs, Specification, STPs, Protocols, and technical reports incorporating appropriate use of statistics. Evaluate data for compliance to procedures and specifications. Identify potential problems and proactively suggest solutions based upon analytical expertise and knowledge of product/process. Provide program compliance and audit support Knowledge, Skills & Competencies / Language Knowledge of Good Laboratory Practices, Good Documentation Practices and Health, Safety & Environment (HSE) requirements pertaining to GMP environment Key experience in method development and impurity profiling of Small Molecules and Solid Oral Dosage Forms. Knowledge on Analytical aspects of Nitrosamine, NDSRIs & other genotoxic Impurities development. Knowledge on transfer of analytical methods of assay, dissolution, estimation of impurities, etc. to Quality Control lab in manufacturing premises Designing and execution of protocols and reports for analytical method, stability and validation, master documents – standard testing procedures, calibration / Qualification protocols, etc. Must have experience with reference standard programs and critical reagents. Knowledge of USP, EP, IP and global compendial regulations & requirements for method life cycle approaches & management. Experience in qualifying (or managing qualification of) critical reagents, qualified materials (such as assay controls), and analytical reference standards. Scientific technical writing ability including authoring and revising SOPs, qualification Protocols, and technical reports Proficient in MS Outlook, Word, and Excel Effective oral and written communication skills (English Language) Qualifications M.Sc. / M. Pharm / Ph. D with specialization in Pharmaceutical Analysis / Pharmaceutical Chemistry / Analytical Chemistry from a reputed university. 4 to 10 years’ experience with technical knowledge & Hands on experience of Sophisticated Analytical instruments like HPLC, GC, IR, UV Spectrophotometer, Mass Spectrometer, Dissolution Tester etc. Excellent knowledge of English language (verbal and written). Beware of Job Scams: Sanofi Fraud Notice: As you conduct your job search, please beware of the possibility that scammers may post fraudulent job openings or send fraudulent communications (email, SMS, WhatsApp or Messenger messages pretending to be from Sanofi) regarding potential job postings or offers in an attempt to encourage the job seeker to disclose financial or personal information. We do not make any payments to or ask candidates for any fees as part of the application process. In most cases you can expect to hear directly from a member of our recruiting team with a legitimate @sanofi.com email address, but you may receive communications from one of our recruiting partners as well. Consequently, you should always conduct research to ensure a posting and/or offer is legitimate and you should never provide personal or financial information unless you are certain that the request is legitimate. If you are concerned that an offer of employment with Sanofi might be a scam, please verify by searching for the posting on the Careers webpage null

Location: 2) Ankleshwar ( ICP-OES & AAS Exp Needed) Handling ICP-OES with a minimum of 2-4 years of experience. Below are the details. Operating, maintaining, and troubleshooting Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES) . Proven expertise in sample preparation, method development, and data interpretation, with a strong background in Instrumentation analysis. Exceptional problem-solving skills and a commitment to ensuring the accuracy and reliability of laboratory results. Develop and validate analytical methods for high-throughput sample analysis, ensuring compliance with industry standards. Conduct routine maintenance and calibration of ICP-OES equipment to optimize performance and minimize downtime. Analyze and interpret data, preparing detailed reports and presenting findings to team members and stakeholders. Maintained accurate laboratory records and conducted regular inventory management of supplies.

Key Responsibilities: Analytical Testing: Conduct routine and non-routine testing of raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis Spectroscopy, FTIR, and microbiological methods. Documentation: Prepare, review, and maintain accurate laboratory records, test reports, and validation documentation in compliance with Good Laboratory Practices (GLP) and regulatory requirements. Quality Assurance: Collaborate with Quality Assurance (QA) to ensure compliance with cGMP (current Good Manufacturing Practices) and regulatory guidelines (FDA, EMA, etc.). Equipment Calibration: Perform calibration, maintenance, and troubleshooting of laboratory equipment. Deviation Management: Investigate deviations, out-of-specification (OOS) results, and implement corrective and preventive actions (CAPA). Method Validation: Assist in the validation and transfer of analytical methods to ensure accuracy, precision, and reproducibility Contact : Kanagavel M | +91 8072654123.

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Division :- Formulation Interview Date:- 05-04-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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.

Job description 1. Candidates will be responsible for Sales of high-tech analytical & Life Science instruments like HPLC, LCMS, GC, GC-MS, UVVis, FTIR, ICPMS, AAS spectrophotometers, Rotary Evaporator, PCR, Digital Droplet PCR, Fermenter, Bioreactor, Liquid handling Systems, Nucleic Acid Extraction etc. 2. Desired candidates profile : The candidate should meet/exceed sales targets, provide accurate sales forecasts, generate leads, deliver timely and accurate reports, and take strategic initiatives to convert inquiries into orders. Products : Analytical Instruments Laboratory Equipments Life Science Instruments Chromatography Columns and Consumables Spectroscopy Accessories and Consumables Required Experience, Skills and Qualifications Qualification: Degree in Science or Engineering. Preferably in Instrumentation, Electronics, Electrical, or Chemical Engineering. An MBA in Marketing can be highly beneficial, along with strong sales skills and a thorough understanding of our products, applications, and support. Additional strengths include proficiency in market research, digital tools, and platforms, as well as strong analytical skills. Location - Hyderabad, Chennai, Bengaluru, Delhi, Chandigarh/Baddi, Haridwar, Ahmedabad About BasilBio BasilBio is a leader in providing innovative laboratory solutions, with a focus on cutting-edge technologies in chemistry, life sciences, and analytical instrumentation. We are looking for a motivated and dynamic professional to join our growing team.

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

A.Responsibilities: Responsible for providing post sale customer on-site application support on GC, GCMS & GCMS-MS. Supporting customer method development / method optimization assistance pertaining to their sample matrices Helping customer with method validation support , Trouble shooting of customers application issues Demonstrating to customers advanced software capabilities and method packages with sample matrices Coordinate with Principals local application lab for any support required to address any unresolved customers application requests Conducting application training to customers chemists for effective use and utilization of the system and software Preparing effective application support reports detailing activities carried out and final result achieved Preparing and making PowerPoint presentations as and when required to customer on application support activity carried out and result achieved B.Key Success Behaviors (Key Competencies): Experience in handling chromatography sampling techniques like Head space Samplers, Thermal Resorption, Pyrolyzer, etc. would be added advantage Should have experience in analytical method development, method optimization, method validation using these techniques for GC, GCMS, GCMSMS. Should have knowledge of application workflows as per industry segment worked

Role & responsibilities Experience in operation and trouble shooting of process in plant. Isolation and purification of different organic compound using column chromatographic and crystallization techniques. Optimize the process parameters, what-if studies, holding studies etc. for scale up. Investigation of OOS/OOT and stability related issues. Analytical development In R&D department Reactions performed like Hydrogenation, Brominating, Oxidation, Reduction and condensation. Handling of Moisture sensitive reactions. Study and understand the project requirements, identifying and collection of suitable literature. Support lab manager to prepare weekly technical reports and other project related technical documents (impurity profile tables, Plant batch data, developmental reports) Executing assigned reactions of project. • Looking after the Safety equipment's management and maintaining it as per regulatory requirement in R&D lab. • Study the MSDS of each chemical using in every new project and make arrangement of Safety equipment's accordingly. Handled HPLC system of Agilent technologies Eriochrome (A.04.07) and version Open Lab cds2.4 • Good in Thin layer chromatography & Column chromatography. • Polymorph characterization with the aid of XRD, DSC, TGA and IR Techniques. • Having good ability to interpret analytical results like NMR, HPLC, GC, LCMS, MASS, IR & UV. Preferred candidate profile Perks and benefits

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-29-03-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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.

Job description for Service Engineer : - 1. The candidate we are looking for must be Engineering graduate as mentioned above. 2. Good English Communication & Confidence. 3. Enthusiastic & willing to make career in Service. Willingness to travel, Learn & grow personally & professionally. 4. Training will be provided for our Instruments which will be handled by you in. 5. It could be Analytical, Laboratory, Contamination Control, Cleanroom Monitoring, Test & Measurement, Validation Setup, HVAC, IAQ, CC, Environment & Ventilation. Your Role : 1. Technical Service Engineer must know Installation, Commissioning, Calibration and Maintenance of various field instruments. 2. Proven analytical and creative problem-solving abilities. 3. Knowledge of Particle Counter, Analytical, Test, HVAC & Indoor Air Quality Instruments, and Online Monitoring Systems CMS/FMS. 4. Create and maintain documentation as it relates to system configuration, mapping, processes, and service records. 5. Planning and Scheduling service visits, installations at PAN India level. 6. Manage cost and time constraints. 7. Able to prioritize and execute tasks in a high-pressure environment. 8. Idea of TCP/IP networking is added advantage. Personality Traits :- 1. Excellent Verbal & Written English Communication. 2. Enthusiastic & active. 3. Capable of making presentations, demonstration of Instruments. 4. Polite & Convincing. Role & responsibilities Preferred candidate profile Perks and benefits

Job Title: Senior QC Chemist (Part-time) Company: Ambica Dhatu Pvt. Ltd. Location: Jalan Complex, Howrah About Ambica Dhatu Pvt. Ltd.: Ambica Dhatu Pvt. Ltd. is a leading company specializing in the manufacturing and quality control of metal alloys and related products. We pride ourselves on maintaining the highest standards in quality and ensuring that our products meet both industry regulations and customer specifications. Position Overview: We are seeking a skilled and experienced Senior QC Chemist to join our dynamic team on a part-time basis. The ideal candidate will be responsible for conducting chemical analysis, and ensuring that all products meet the required quality standards. This position requires a deep understanding of chemical processes, quality control systems, and the ability to manage both routine and complex testing procedures. Key Responsibilities: Perform chemical analysis of raw materials, in-process materials, and finished products to ensure compliance with specifications. Conduct tests on materials using advanced laboratory instruments and techniques, including spectrophotometers, chromatography, and other chemical testing equipment. Maintain accurate and detailed records of test results and ensure all data is properly documented and reported. Develop and implement quality control procedures, ensuring adherence to industry standards and company policies. Collaborate with production teams to resolve any quality-related issues and provide technical support. Ensure compliance with environmental, health, and safety regulations. Review and update SOPs (Standard Operating Procedures) to improve lab practices and efficiency. Manage inventory of chemicals and lab supplies and ensure proper storage and handling. Prepare reports on testing results, including any deviations from the standard and corrective actions taken. Participate in regular audits and inspections of laboratory processes and practices. Qualifications and Requirements: Bachelors or Master’s degree in Chemistry, Chemical Engineering, or a related field. Minimum of 5 years of experience in a quality control or laboratory-based role, preferably in the manufacturing or chemical industry. Strong understanding of laboratory techniques and equipment used for chemical testing. Proven experience in handling complex QC tasks and leading quality improvement initiatives. Ability to work independently with minimal supervision and manage time effectively. Excellent analytical, problem-solving, and decision-making skills. Familiarity with ISO, GMP, or other quality management systems is preferred. Strong written and verbal communication skills. Attention to detail and a commitment to ensuring the highest standards of quality. Working Hours: Part-time, flexible hours (to be discussed during the interview process). Compensation: Competitive salary based on experience

Location: 1) Greater Noida ( Only ICP-OES Exp Needed) 2) Ankleshwar ( ICP-OES & AAS Exp Needed) Handling ICP-OES and Atomic Absorption Spectroscopy with a minimum of 2-4 years of experience. Below are the details. Operating, maintaining, and troubleshooting Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES) and AAS instruments. Proven expertise in sample preparation, method development, and data interpretation, with a strong background in Instrumentation analysis. Exceptional problem-solving skills and a commitment to ensuring the accuracy and reliability of laboratory results. Develop and validate analytical methods for high-throughput sample analysis, ensuring compliance with industry standards. Conduct routine maintenance and calibration of ICP-OES and AAS equipment to optimize performance and minimize downtime. Analyze and interpret data, preparing detailed reports and presenting findings to team members and stakeholders. Maintained accurate laboratory records and conducted regular inventory management of supplies. Should posses experience and knowledge on ISO17025 and ISO9001 Quality Management system.

Role & responsibilities 1. Testing of Ores and Minerals, heavy metal, coal etc. 2. Perform accreditation procedure from NABL & MOEF &CC (application, MU, calibration, all applicable relevant records) 3. Environmental monitoring and testing 4. Handling & working with testing equipment AAS, Hg-Analyser, spectrophotometer, bomb calorimeter, Gas Chromatography and other basic equipment. 5. Thorough knowledge of microbiological Testing Desirable: ISO 17025 training (4 days) Preferred candidate profile 1-5years experienced in industrial mineral testing & analysis Must have exposed in NABL Labs MSc Chemistry preferred Willing to relocate to Udaipur,Rajasthan Male candidate preferable with good communication skills Interested candidates can either apply here or can share CV at pooja.relhan@golcha.com

Lead lab operations at a top ferroalloys producer! Seeking an experienced lab in charge to ensure precision in quality control. Salary up to 70K + benefits. Apply now! Company Name: V.A. POWER & STEELS PVT.LTD. Job Title: Lab In-Charge Location: 143-144, O.P. Jindal Industrial Park, Punjipathara, District Raigarh, Chhattisgarh - 496111 About the Company: VA Power & Steels Pvt. Ltd. is a premier producer of high-quality manganese alloys, with over a decade of industry expertise. Located at Jindal Industrial Park near Raigarh, Chhattisgarh, our facility operates two smelters with a combined 16.5 MVA capacity, producing 25,000 tonnes of manganese alloys annually. With over 50% of our output exported, we are committed to delivering top-tier products while adhering to international quality standards. The Role The company is looking for an experienced lab in charge to lead our laboratory operations, ensuring precision in chemical analysis and quality checks for raw materials and finished goods. If you are meticulous, and analytical, and thrive in a structured environment, this role is for you. What You Will Do Develop and refine material sampling and lab testing systems for accuracy and efficiency. Maintain comprehensive documentation to ensure audit transparency and compliance. Conduct chemical and physical property tests to uphold product quality. Ensure strict adherence to industry standards and laboratory protocols. Collaborate with stakeholders for timely decision-making and reporting. Who You Are Educational Background: Bachelor's or Masters degree in Chemistry. Experience: 10-15 years in a similar role within the ferroalloys or related industry. Technical Skills: Proficiency in laboratory testing methods, equipment calibration, spectrophotometry, titration, XRF (X-ray fluorescence), ICP-OES (Inductively Coupled Plasma Optical Emission Spectrometry), and wet chemical analysis. Functional Skills: Strong analytical abilities, integrity, attention to detail, and effective communication. Integrity: Committed to honesty, transparency, and adherence to ethical standards in lab operations. What's in It for You? Competitive Salary : 70,000 per month. Rent-Free Accommodation: Hassle-free living near the workplace. 52 Weekly Offs + Leave Policy : Work-life balance ensured. Accidental Coverage Benefits: Financial security for peace of mind. Join VA Power & Steels Pvt. Ltd. and contribute to an organization that values precision, innovation, and reliability in the production of high-grade manganese alloys. Email your resume at recruitment@geebeegroup.in and be part of something exceptional!

Candidate will be expected to fully manage the ICP-OES/MS, AAS instrument, including its operation, maintenance, calibration, and troubleshooting. The role requires preparing standard solutions and samples for analysis, performing metal analysis. Required Candidate profile The candidate will be responsible for the operation, maintenance, and troubleshooting of the ICP-OES/MS, AAS instrument in a NABL-accredited laboratory.

Roles and Responsibilities Conduct quality control analysis using HPLC, GC, UV, spectrophotometer, sterile techniques, and other relevant methods. Ensure compliance with USFDA, GMP, GLP regulations during regulatory audits. Develop and maintain SOPs for laboratory operations and testing procedures. Collaborate with cross-functional teams to resolve quality issues and improve processes. Perform stability studies on APIs and finished products as required. Desired Candidate Profile 2-7 years of experience in a pharmaceutical industry setting with expertise in QC analysis. MS/M.Sc(Science) degree in Chemistry or related field; Strong understanding of analytical instruments such as HPLC, GC, UV spectrometer etc., and ability to operate them effectively.

M.Sc. – Chemistry (OR) M. Sc.- Environmental Sci. • Sampling and Analysis of Raw Material • Analysis of Water and Wastewater sample/ Parameters. • Calibration of pH meter, Turbidity Meter & Karl Fischer • Operation of UV Visible Spectrophotometer