165 Spectrophotometer Jobs - Page 3

Job Title: Lab Chemist – Ayurvedic Industry Location: LAWRENCE ROAD, SHAKURPUR, DELHI Company Name: GOBIND RAM KAHAN CHAND Job Description: We are looking for an experienced and qualified Lab Chemist to join our Ayurvedic manufacturing unit. The ideal candidate should have strong knowledge in herbal testing and formulation, with a deep understanding of AYUSH and GMP standards. The candidate will be responsible for quality testing, analysis, and compliance documentation of Ayurvedic products. Key Responsibilities: Perform testing of raw materials, in-process samples, and finished Ayurvedic products Maintain lab documentation, reports, and analysis records Ensure testing procedures comply with AYUSH and GMP standards Develop and validate testing methods for herbal formulations Operate and maintain laboratory equipment like HPLC, UV Spectrophotometer, etc. Coordinate with R&D, Production, and QA/QC departments Conduct stability, microbial, and heavy metal testing Prepare Certificate of Analysis (COA) and product documentation Qualifications and Experience: Education: B.Sc. or M.Sc. in Chemistry, Biochemistry, or Pharmaceutical Sciences Experience: Minimum 3 to 7 years in an Ayurvedic, Herbal, or Pharma industry lab Knowledge of herbal ingredients and AYUSH regulatory standards is essential Skilled in analytical instruments and classical testing methods Strong communication and documentation skills Salary Package: Salary: Rs. 30,000 UPTO per month (negotiable as per experience and expertise) Benefits: Yearly appraisals, performance bonuses, paid leaves, and professional growth Job Types: Full-time, Permanent Pay: Up to ₹30,000.00 per month Schedule: Day shift Morning shift Night shift Rotational shift Work Location: In person

Job Title: Middle-Level Analyst – HPLC, UV, Dissolution, Assay, RS, and Method Validation Company: KMS Healthcare Pvt. Ltd. Department: Quality Control / Analytical R&D Experience: 3-7 years in pharmaceutical analysis Job Summary: We are seeking an experienced Analyst with expertise in HPLC, UV-Vis spectroscopy, dissolution testing, assay, related substances (RS), and method validation as per ICH guidelines . The candidate will be responsible for conducting analytical testing, preparing protocols/reports, and ensuring compliance with regulatory standards. Key Responsibilities:1. Analytical Testing & Instrumentation: Perform routine and non-routine analysis using HPLC, UV-Vis, dissolution apparatus , and other lab instruments. Conduct assay, related substances (RS), dissolution, and stability testing as per pharmacopeial methods (USP/EP/BP/IP). Troubleshoot and maintain analytical instruments (HPLC, UV spectrophotometer, dissolution apparatus). 2. Method Validation & Transfer: Prepare and execute method validation/verification protocols (Accuracy, Precision, Linearity, Specificity, LOD/LOQ, Robustness) as per ICH Q2(R1) . Support method transfer activities between labs or sites. 3. Documentation & Compliance: Prepare analytical reports, validation protocols, and reports in compliance with GMP/GLP . Review and ensure data integrity (ALCOA+ principles). Follow SOPs, pharmacopeial guidelines (USP/EP), and ICH requirements . 4. Regulatory & Audits: Support regulatory submissions (ANDAs, DMFs) with analytical data. Participate in internal/external audits (FDA, WHO, MHRA). 5. Cross-Functional Collaboration: Work with QA, R&D, and production teams for investigations (OOS/OOT, deviations). Train junior analysts on analytical techniques and compliance. Qualifications & Skills: Education: Bio Technology/ M.Sc./B.Pharm/M.Pharm in Chemistry/Pharmaceutical Sciences. Experience: 3-7 years in pharmaceutical QC/ADL labs , with hands-on experience in: HPLC/UPLC (Method development/validation preferred). UV-Vis spectroscopy, dissolution testing (Apparatus I/II). Assay, RS, forced degradation studies. Regulatory Knowledge: ICH, USFDA, GMP, GLP. Software: Empower, LabSolutions, Dissolution software. Soft Skills: Detail-oriented, problem-solving, teamwork. Preferred: Experience in oral solid dosages (tablets/capsules) . Knowledge of impurity profiling, stability studies (ICH Q1A). Why Join Us? Opportunity to work in a GMP-compliant lab with advanced instrumentation. Career growth in analytical development/validation. Exposure to global regulatory standards. Job Type: Full-time Location: Door No.6, Kamarajar St, East Tambaram, Selaiyur, Chennai, Tamil Nadu 600059 Job . Job Type: Full-time Pay: ₹30,000.00 - ₹60,000.00 per month Schedule: Day shift Morning shift Work Location: In person Expected Start Date: 25/07/2025

Job Title: Middle-Level Analyst – HPLC, UV, Dissolution, Assay, RS, and Method Validation Company: KMS Healthcare Pvt. Ltd. Department: Quality Control / Analytical R&D Experience: 3-7 years in pharmaceutical analysis Job Summary: We are seeking an experienced Analyst with expertise in HPLC, UV-Vis spectroscopy, dissolution testing, assay, related substances (RS), and method validation as per ICH guidelines . The candidate will be responsible for conducting analytical testing, preparing protocols/reports, and ensuring compliance with regulatory standards. Key Responsibilities:1. Analytical Testing & Instrumentation: Perform routine and non-routine analysis using HPLC, UV-Vis, dissolution apparatus , and other lab instruments. Conduct assay, related substances (RS), dissolution, and stability testing as per pharmacopeial methods (USP/EP/BP/IP). Troubleshoot and maintain analytical instruments (HPLC, UV spectrophotometer, dissolution apparatus). 2. Method Validation & Transfer: Prepare and execute method validation/verification protocols (Accuracy, Precision, Linearity, Specificity, LOD/LOQ, Robustness) as per ICH Q2(R1) . Support method transfer activities between labs or sites. 3. Documentation & Compliance: Prepare analytical reports, validation protocols, and reports in compliance with GMP/GLP . Review and ensure data integrity (ALCOA+ principles). Follow SOPs, pharmacopeial guidelines (USP/EP), and ICH requirements . 4. Regulatory & Audits: Support regulatory submissions (ANDAs, DMFs) with analytical data. Participate in internal/external audits (FDA, WHO, MHRA). 5. Cross-Functional Collaboration: Work with QA, R&D, and production teams for investigations (OOS/OOT, deviations). Train junior analysts on analytical techniques and compliance. Qualifications & Skills: Education: Bio Technology/ M.Sc./B.Pharm/M.Pharm in Chemistry/Pharmaceutical Sciences. Experience: 3-7 years in pharmaceutical QC/ADL labs , with hands-on experience in: HPLC/UPLC (Method development/validation preferred). UV-Vis spectroscopy, dissolution testing (Apparatus I/II). Assay, RS, forced degradation studies. Regulatory Knowledge: ICH, USFDA, GMP, GLP. Software: Empower, LabSolutions, Dissolution software. Soft Skills: Detail-oriented, problem-solving, teamwork. Preferred: Experience in oral solid dosages (tablets/capsules) . Knowledge of impurity profiling, stability studies (ICH Q1A). Why Join Us? Opportunity to work in a GMP-compliant lab with advanced instrumentation. Career growth in analytical development/validation. Exposure to global regulatory standards. Job Type: Full-time Location: Door No.6, Kamarajar St, East Tambaram, Selaiyur, Chennai, Tamil Nadu 600059 Job . Job Type: Full-time Pay: ₹30,000.00 - ₹60,000.00 per month Schedule: Day shift Morning shift Work Location: In person Expected Start Date: 25/07/2025

Key Responsibilities: - Lead Analytical Testing: Oversee and perform routine and complex analytical tests for raw materials, in-process materials, and finished products (liquid, powder, external formulations, tablets, and capsules). - HPLC, GC, UV, and Other Analytical Techniques: Expertly operate and maintain advanced analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, and other laboratory equipment to ensure the accurate analysis of veterinary drug formulations. - Method Validation & Development: Lead the development, optimization, and validation of analytical methods for veterinary products. Ensure methods meet regulatory standards and are suitable for routine use in QC testing. - SOPs and Documentation: Draft, review, and revise Standard Operating Procedures (SOPs) for analytical methods and testing protocols. Ensure comprehensive documentation for all testing procedures and maintain compliance with regulatory requirements. - Regulatory Compliance: Ensure all QC activities comply with national and international regulations, such as WHO-GMP, GLP, and other relevant standards. Ensure product testing adheres to pharmacopeial guidelines and regulatory expectations. - Training & Mentoring: Lead, train, and mentor junior QC staff in analytical testing procedures, method development, and regulatory compliance. Foster a collaborative and knowledge-sharing environment within the QC department. - Quality Control Management: Oversee the smooth operation of the QC laboratory, ensuring it functions at optimum capacity, maintaining proper calibration and validation of analytical equipment. - Investigations & Troubleshooting: Investigate and resolve analytical issues, deviations, and out-of-spec results. Perform root cause analysis and implement corrective actions as needed. - Reporting & Data Analysis: Prepare and present clear, accurate analytical reports, data summaries, and trend analysis. Communicate findings to senior management and other departments. - Product Release: Participate in the review and approval of analytical data for the release of finished products, ensuring they meet all specifications and quality standards. - Audit and Inspection Readiness: Ensure the laboratory and documentation meet internal and external audit requirements. Act as the subject matter expert during inspections and audits by regulatory authorities. Qualifications & Skills: - Education: Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field. - Experience: Minimum 5-8 years of experience in analytical testing, with at least 3 years in a supervisory or leadership role. Experience in the veterinary drug formulation industry is highly preferred. - Technical Skills: o Extensive experience with HPLC, GC, UV, and other analytical test equipment. o Knowledge of analytical method development and validation for pharmaceutical formulations. o Proficient in drafting SOPs, test protocols, and detailed analytical reports. o In-depth understanding of regulatory compliance (WHO-GMP, GLP, pharmacopoeial standards). Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,500,000.00 per year Schedule: Day shift Experience: QC Head/Manager: 5 years (Preferred) HPLC: 5 years (Preferred) GC: 5 years (Preferred) UV: 5 years (Preferred) analytical testing: 3 years (Preferred) drug formulation industry: 3 years (Preferred) Work Location: In person

Qualification : M. Pharmacy (Pharmaceutical analysis Experience : 3-4 yrs. (Formulation experience) Sound knowledge of Assay & Dissolution, Analytical method development for tablets, capsules, oral solutions, ICH stability testing, Water HPLC, UV-visible spectrophotometer, KF Auto tiltrotor, Analytical method validations, transfer and verifications as per ICH guidelines and USP/BP guidelines, Analysis of in-process, stability & protocol driven samples. Reports, Protocols and STP, SOP’s Preparation. GLP Activities. Chromatographic software like Empower Working Location: Balanagar (Hyderabad) Interested people Sent the updated resume to recruitment@novickbio.com. Job Type: Permanent Pay: ₹400,000.00 - ₹500,000.00 per year Work Location: In person Application Deadline: 20/07/2025 Expected Start Date: 11/07/2025

Department: Dyeing - Lab Reporting To: Head - Dyeing Department Job Summary: The Dyeing Lab Incharge will be responsible for overseeing the entire operations of the dyeing laboratory, with a primary focus on polyester dyeing. This role involves managing lab dip development, improving Right First Time (RFT) performance, upgrading lab infrastructure, and ensuring accurate shade matching and testing. The candidate must have hands-on experience with lab equipment used in polyester dyeing and should be capable of leading initiatives to enhance lab efficiency, lab-to-bulk reproducibility, and turnaround time. Key Responsibilities: 1. Lab Operations & Shade Development: Manage end-to-end lab operations including shade matching, recipe formulation, and lab dip development. Ensure accurate and timely submission of lab dips as per customer or internal requirements. Maintain consistency and reproducibility from lab to bulk production. 2. RFT (Right First Time) Improvement: Analyze RFT trends and identify root causes for deviations. Work closely with the dyeing production team to align recipes and processes. Standardize lab procedures and recipe management systems to improve RFT. 3. Equipment & Testing Management: Operate, maintain, and calibrate dyeing lab equipment such as: o Infrared dyeing machines o Spectrophotometers (Datacolor/Minolta) o Fastness testing machines o GSM, shrinkage, and pH testing tools Introduce and implement best practices for equipment handling and testing protocols specific to polyester dyeing. 4. Lab Upgrade & Efficiency Enhancement: Identify gaps in current lab setup and recommend technology or equipment upgrades. Improve lab processes to reduce lead time, enhance accuracy, and reduce rework. Lead trials for new dyes, auxiliaries, and methods to enhance polyester dyeing results. 5. Documentation & Reporting: Maintain records of lab dips, test reports, and approved recipes. Generate RFT performance reports, lab-to-bulk deviation logs, and shade approval timelines. Ensure compliance with customer specifications, internal SOPs, and audit requirements. 6. Team Leadership & Coordination: Supervise lab assistants and junior chemists. Train lab personnel in shade matching, polyester dyeing techniques, and machine operation. Coordinate with marketing, production, and QA teams for shade approvals and technical support. Skills & Qualifications: Educational Qualification: Diploma / B.Tech in Textile Chemistry, Textile Technology, or related field. Experience: 8-10 years of experience in dyeing lab operations, with a strong focus on polyester dyeing. Technical Expertise: o In-depth knowledge of disperse dyes and polyester dyeing behavior. o Strong command over color matching, spectrophotometer usage, and fastness testing. o Ability to troubleshoot lab-to-bulk mismatches and process inefficiencies. Other Skills: o Proficient in lab management software and shade libraries. o Excellent organizational, analytical, and leadership skills. o Strong coordination abilities with cross-functional teams.

Key Responsibilities:  Perform chemical analysis of bulk and finished products (mainly Tablets).  Conduct weight variation tests during in-process and final stages.  Assist in stability studies using Dissolution & Disintegration apparatus.  Operate and calibrate UV-Spectrophotometer, Dissolution, and Disintegration test machines.  Maintain log books, SOPs, and ensure regulatory documentation.  Prepare bulk and finished product reports. Ideal Candidate:  B.Sc. / M.Sc. in Chemistry or related field.  Keen interest in pharmaceutical quality control.  Strong documentation habits and attention to detail.  Willing to learn and grow in a GMP-regulated environment. Job Type: Full-time Pay: ₹15,000.00 - ₹22,000.00 per month Schedule: Day shift Work Location: In person

Title: Senior Officer Custom Field 2: 2727 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 Experience in chemical analysis like, titration, moisture, LOD, sulphated ash, TLC IR, SOR, Clarity of solutions and quantitative solubility tests Exposure of GMP / GLP / GDP in laboratory. Knowledge of separation techniques in chemical separation in chromatography in Normal and reversed phase systems Preparation of Standard operating procedures (SOP) for all the instruments, equipment and procedures. Qualification of instruments Job Segment: Chemical Research, Laboratory, Engineering, Science

Textile testing engineer Education qualification - BTech( textile engineering) / Msc Chemistry Textile Physical Lab (Strength properties) testing as per International standard/Buyer's specific standards. Experience in textile testing, test audits, test validation, various test/ brand protocols training, various correlations & laboratory internal audits. The person has to work on Quality systems, Documentation, Calibration, Correlations & Lab Operations. Flammability testing as per the International standard Color evaluation, Spectrophotometer evaluation. Well familiar with the Grey scale rating for different colour fastness evaluation. To carry out testing on yarn and fiber as per Indian standards.

Key Objective: Establish and manage a functional textile lab that supports internal quality validation, maintains color standards, coordinates lab dips and test results with outsourced vendors, and ensures lab-to-bulk color consistency. Mandatory experience for 5-7 years in woven fabric and garment testing . 1. Lab Setup & Management Plan and set up the textile testing and color lab, including layout, equipment, consumables, and safety protocols. Identify and procure essential testing and shade assessment tools (GSM cutter, pH meter, shrinkage markers, light box, spectrophotometer, etc.). Develop SOPs and maintain calibration schedules for lab instruments. 2. Shade Development & Color Matching Receive shade references (Pantone, swatch, digital) from merchandising or buyers. Coordinate lab dip development with outsourced dyeing/printing vendors. Evaluate lab dips (visual and Delta E) and provide feedback to vendors. Maintain a physical and digital shade library with buyer-approved standards and bulk references. 3. Testing Oversight (Vendor & In-House) Verify and document fabric testing results received from vendors (colorfastness, shrinkage, pH, etc.). Conduct basic in-house fabric checks for GSM, dimensional stability, appearance, and color consistency. Identify deviations in shade, quality, or fastness and communicate with QC and merch teams. 4. Documentation & Internal Approvals Record all lab dip approvals/rejections, test reports, and vendor submissions systematically. Issue internal lab approvals for cutting/production once shades are cleared. Maintain traceability between approved shade and bulk production lot. 5. Vendor & Team Coordination Serve as technical liaison between merchandisers, dyeing units, printing vendors, and embroidery houses. Guide assistants (if any) on shade swatch prep, documentation, and lab discipline. Communicate recurring quality or color issues to relevant departments. 6. Lab Hygiene & Safety Ensure lab cleanliness, organization, and proper storage of samples, dyes, and chemicals. Follow material safety guidelines and ensure PPE usage where necessary. Desirable Skills: Good eye for color differentiation and precision. Familiarity with woven and knitted fabric behavior. Understanding of sustainable dye practices and certifications (GOTS, OEKO-TEX). Experience working with external processing units. Competence in basic fabric testing and Excel-based documentation. Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Paid time off Provident Fund Schedule: Morning shift Supplemental Pay: Performance bonus Yearly bonus Ability to commute/relocate: Erode, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Preferred) Experience: Textile Laboratory: 10 years (Required) Work Location: In person Expected Start Date: 01/08/2025

About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Analytical Method Development & Validation: Develop and optimize analytical methods for pharmaceutical compounds using HPLC, GC, UV-Vis, and other analytical techniques. Perform method validation studies including accuracy, precision, linearity, specificity, and robustness testing. Transfer analytical methods between laboratories and ensure successful implementation. Troubleshoot analytical methods and resolve technical issues. Sample Analysis & Testing: Conduct routine analysis of raw materials, intermediates, and finished pharmaceutical products. Perform quantitative and qualitative analysis following established protocols and regulatory guidelines. Execute stability studies and analyze samples at designated time points. Instrumentation & Maintenance: Operate and maintain analytical instruments including HPLC, GC, GC-MS, FTIR, UV-Vis spectrophotometers. Perform routine calibration. Troubleshoot instrument issues and coordinate with service technicians when needed. Ensure proper documentation of instrument performance and maintenance activities. Data Management & Reporting: Analyze and interpret analytical data using statistical methods and software. Prepare technical reports, certificates of analysis, and regulatory submissions. Maintain accurate laboratory records and electronic data systems. Knowledge & Experience Master's degree in Analytical Chemistry, Chemistry, or related field. 2 - 4 years of relevant experience in pharmaceutical, chemical, or analytical laboratory settings. Strong foundation in analytical chemistry principles and techniques. Preferred Qualifications Experience with advanced analytical techniques (DSC, TGA). Previous experience in pharmaceutical or biotech industry. Understanding of stability testing and forced degradation studies. Knowledge of cleaning validation by UV / HPLC. Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans .

lab chemist required for a MNC food company Qualification - Any food degree or diploma Exp- min 2 yrs Salary- upto 30k Location- Kundli, sonipat

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