98 Spectrophotometer Jobs - Page 2

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities. Brief Job Overview This is a non-supervisory position to support development of Reference materials. The successful applicant in this role will work on projects including Analytical Method Development for in process samples for synthetic lab. The successful candidate will also perform a variety of non-routine and routine analytical tests, maintains safety & GLP environment in the lab including evaluation of reference standards, development/validation (as per requirement) of official methods, stability studies and research projects in analytical department How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The Technical Associate Has The Following Responsibilities [60%] Support to reaction monitoring, scale up and final analysis of samples as per monograph / in-house procedures including method development if required. Prepare development reports for Synthetic Support projects. Involve in project acceptance. Execute projects per the approved test protocols if assigned. [15%] Prepare, execute, and complete IQ/OQ/PQ of new instruments. Indent the required glass ware, chemicals, and columns for the ARD projects. Maintain GLP & implement safety procedures while working in Lab. Perform other Projects whenever free from ARD activities. Perform other duties as assigned [10%] Responsible for preparation of SOPs, protocols, reports, etc. Ensure the projects requirements by coordinating with the Purchasing department. Responsible for preparation of the records and documents. Ensure that the calibrations of the equipment’s are performed as per the schedule [10%] Preparation and planning for ISO-9001 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner. Taking up any other additional responsibilities assigned by supervisor on a proactive basis and allotting additional responsibilities to the reporting staff in consultation with the supervisor. Participates in USP cross-functional teams as appropriate. [5%] Practice Diversity, Equity, Inclusion, and Belonging principles at USP India. Who is USP Looking For? Example The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: MSc. in Analytical Chemistry / Organic Chemistry/M. Pharma, having 0-1 years of experience in Analytical Research and Development. Must have hands on experience in working with chemical methods and handling instruments like HPLC, wet chemistry, etc. Experience in analytical testing and development with focus on process analytical chemistry. Exposure to GMP/GLP environment and documentation procedures required. Excellent technical writing and verbal communication skills are required. Additional Desired Preference Knowledge of handling FTIR and UV Spectrophotometer will be added advantage General chapter information, ELN, Empower and NuGenesis will be added advantage. Able to communicate effectively with both internal and external customers. Preferably familiar with electronic notebook documentation of experimental procedures. Good interpersonal skills and proven ability to function in a team-oriented environment are necessary. Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration. Supervisory Responsibilities NA Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP Job Category Chemistry & Scientific Standards Job Type Full-Time Show more Show less

Hiring Technical Service Specialist (Biotech/Lab Instruments) – Install, maintain & troubleshoot lab instruments. Promote products, handle AMC & support sales. B.E/B.Tech in Biomedical/Biotech. 1+ yr exp. Two-wheeler must. hr@genetechnologies.co.in

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Job Summary: We are seeking a motivated and detail-oriented Junior Chemist to join our laboratory team in Kolkata. The ideal candidate will hold a B.Sc. in Chemistry and will assist in conducting chemical analyses, preparing samples, and supporting senior chemists in R&D or quality control activities. Key Responsibilities: Conduct routine chemical tests and analyses in accordance with standard procedures Prepare chemical solutions and reagents under supervision Maintain accurate records of experiments and results Operate and calibrate laboratory equipment as required Assist in quality control and research activities Ensure compliance with laboratory safety protocols and standards Maintain cleanliness and organization of the lab environment Minimum Qualifications: Bachelor of Science (B.Sc.) in Chemistry from a recognized institution Basic understanding of laboratory practices and chemical handling Freshers or candidates with up to 1 year of experience are welcome to apply Key Skills: Strong analytical and problem-solving abilities Attention to detail and accuracy in lab work Good communication and teamwork skills Familiarity with MS Office (Excel, Word) Preferred Qualifications (Optional): Internship or project work in a chemical laboratory Familiarity with laboratory instruments such as pH meter, spectrophotometer, etc. Job Type: Full-time Pay: ₹10,000.00 - ₹17,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Position Title : Senior Scientific Officer/Scientific Officer- Quality Control- Electrophoresis and Chromatography lab Educational Qualification : M.Sc. / M.Tech -Biotechnology/ Microbiology Experience : 3 to 7 years Job Summary Senior Scientific Officer/Scientific Officer- Electrophoresis and Chromatography Lab (Quality Control) shall be responsible for ensuring the quality and efficacy of vaccine formulations at Vaccine Drug Substance Plant, Lalru (Punjab). This position will be responsible for overseeing the operation of HPLC, Weighing Balance operation, pH meter, Operation of densitometer, operation of tube heating block, testing of CRM-197 Protein by HPLC and SDS Page etc. Responsibilities: 1. Hands on Knowledge for operation of HPLC, Weighing Balance operation, pH meter, Operation of densitometer, operation of tube heating block, etc. 2. Hands on experience for testing of CRM-197 Protein by HPLC and SDS Page. 3. Hands on experience for testing of Free Carrier protein by HPLC on HiBTT, HiBTi conjugate and Pneumo conjugate 4. Hands on experience for testing of Molecular Size by HPLC on HiBTT, HiBTi conjugate and Pneumo conjugate 5. Ensure online documentation as per good documentation process. 6. Experience on Method validation for different products 7. Experience for evaluation of LOD/LOQ for rinse samples 8. Verification of Packing and consumables for Production department 9. Testing of Raw material and release. 10. Review of Analytical data’s tested for HPLC and Raw materials. 11. Proficient in analytical procedures and analytical method validations 12. Monitoring of ongoing testing activities on shop floor. 13. Issuance of Reference standards, Retention sample and Stability Sample. 14. Review of analytical data, capability to analyze the raw data of HPLC, GC, spectrophotometer etc JOB DESCRIPTION Name of Dept. Quality Control – Electrophoresis and Chromatography Lab. 15. Right allocation of manpower in shift working and monitoring of assigned task with optimum output. 16. Ensure Quality and quantity of consumables, Solutions with adequate usage & timely delivery to different manufacturing processes. 17. Right & Timely Documentation including SOPs, Change Controls, Deviations, Incidents, CAPA, Risk Assessments, in preview of PQS in view to regulatory guidelines & expectations. 18. Ensure zero non- compliance & zero data integrity in documentation. 19. Ensure regular maintenance of all equipment`s of production by engineering to achieve zero-breakdown. 20. Coordination with intra departmental activities in compliance to support/execution. Competencies Required: 1. Effective Communicator. 2. Motivate Team and Enable High Performance. 3. Effective Performance Reviews of the Team and their Training. 4. Must understand the team needs at the time testing, sample preparation 5. Must understand Sterile Operations, Scientific practices, analytical techniques & process criticalities of Vaccine manufacturing. 6. Analytical approach – Good in trend analysis, data evaluation & process calculations. 7. Adequate, Timely & Quality deliverance/ Output within stipulated timeframe. 8. Thorough understanding of PQS & its compliances with risk based approach. Show more Show less

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India Show more Show less

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India Show more Show less

Job Title: Food Testing Analyst – Chemical Division Location: Mohali Job Summary: We are seeking a skilled and detail-oriented Food Testing Analyst to join our Chemical Division . The ideal candidate will be responsible for performing chemical analysis of food and beverage products using standard methods and modern laboratory instruments. The role requires a solid understanding of food chemistry, regulatory compliance, and laboratory best practices. Key Responsibilities: · Conduct qualitative and quantitative chemical testing of food and beverage samples for parameters such as moisture, fat, protein, ash, pH, acidity, preservatives, and contaminants. · Operate and maintain analytical instruments including: o High-Performance Liquid Chromatography (HPLC) o Gas Chromatography (GC/GC-MS) o Atomic Absorption Spectrophotometer (AAS) o UV-Vis Spectrophotometer, FTIR, Karl Fischer Titrator, Muffle Furnace, etc. Prepare reagents, standard solutions, and samples as per established protocols. Record and analyze test results with accuracy and attention to detail. Document all activities and maintain complete and accurate test records as per ISO 17025 and regulatory guidelines. Ensure compliance with applicable food safety regulations such as FSSAI, BIS, and Codex Alimentarius. Adhere to Good Laboratory Practices (GLP) and safety procedures. Participate in method validation, proficiency testing, and internal audits. Maintain a clean and organized laboratory work environment. Qualifications: B.Sc. or M.Sc. in Chemistry, Analytical Chemistry, Food Technology, or a related field. 1–3 years of relevant experience in a chemical testing laboratory, preferably in the food sector. Strong working knowledge of food chemistry and chemical testing procedures. Hands-on experience with advanced analytical instruments. Familiarity with ISO 17025 standards and laboratory documentation practices. Key Skills: Proficiency in using laboratory instruments and interpreting test data. Strong analytical and problem-solving abilities. Attention to detail and commitment to accuracy. Ability to follow standard operating procedures and regulatory protocols. Good communication and teamwork skills. Share Resume on Email : hritc27@gmail.com Job Types: Full-time, Permanent Pay: From ₹15,000.00 per month Schedule: Day shift Fixed shift Morning shift Work Location: In person

Job Title: Quality Control Executive – Ayurveda Products Department: Quality Control (QC) Location: Kundli Job Summary: We are seeking a detail-oriented and experienced Quality Control Executive to ensure the quality, safety, and compliance of Ayurvedic products. The QC Officer will be responsible for implementing and maintaining testing protocols for raw materials, in-process samples, and finished products according to GMP and regulatory standards applicable to Ayurveda and herbal formulations. Key Responsibilities: Conduct routine quality checks and testing of raw materials, packaging materials, in-process samples , and finished Ayurvedic products . Ensure compliance with AYUSH regulations , GMP , and ISO standards where applicable. Maintain and calibrate lab instruments such as HPTLC, UV-Vis Spectrophotometer, pH meters, etc. Prepare and maintain Standard Operating Procedures (SOPs) , test reports , COAs , and specifications for materials and products. Conduct microbiological testing and stability studies as required. Collaborate with the R&D, production , and QA departments for troubleshooting and quality-related investigations. Handle non-conformance reports (NCRs) and support in CAPA implementation . Review batch manufacturing records (BMRs) and ensure quality documentation is in place. Support in regulatory audits (AYUSH, FSSAI, WHO-GMP, etc.) and third-party inspections. Requirements: Education: B.Sc. / M.Sc. in Chemistry, Microbiology, Biotechnology, or B.Pharm / M.Pharm (Ayurveda or Pharmaceutics preferred). Experience: 2–5 years of experience in Quality Control in an Ayurvedic / herbal / pharmaceutical company . Skills: Knowledge of Herbal Pharmacopoeia , Ayurvedic raw materials, and formulations. Familiarity with regulatory frameworks like AYUSH , WHO-GMP , and FSSAI . Good analytical, problem-solving, and documentation skills. Proficiency in laboratory practices and equipment handling. Preferred Qualifications: Experience with HPTLC , TLC , moisture analysis , ash value , and extractive value testing. Knowledge of modern analytical techniques used in herbal product testing. Basic understanding of Ayurveda / Unani / herbal systems . Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person

Role & responsibilities 1. He shall be responsible to undertake training from the Section in Charge and the senior Analyst to make independent to carry out analysis. 2. He shall report to the senior analyst or analyst if any chemical, reagents or reference material is not available as per the requirement to carry out the analysis. 3. He shall be responsible to analyse samples received as per the specifications and for reporting of the results under the supervision of the senior analyst. 4. He shall be responsible to follow the quality system as per the policies laid down in the quality manual. 5. He shall be responsible for the preparation and standardization of the chemicals under the guidance of the senior analyst or analyst. 6. He shall be responsible to ensure proper documentation of all the data and its maintenance under the guidance of senior analyst or analyst. 7. He shall be responsible to follow the quality policies as per ISO/IEC17025, cGMP, GLP under the supervision of section In-charge or senior analyst. 8. He shall be responsible to perform all the chemical analysis. 9. He shall be responsible for operation, maintenance, timely calibrations of the following instruments: Weighing Balances pH and Conductivity Meter Melting Point Apparatus FTIR Instrument TOC Analyser Hot air ovens and Vacuum Oven Muffle furnace Disintegration Tester Dissolution Tester UV spectrophotometer Polarimeter Refractometer KF Auto titrator Melting point apparatus Tap density apparatus Friabilator

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

The candidate will perform lab tests, validate methods, analyze results, and generate reports. Strong knowledge of chemical analysis, lab safety, and documentation standards is essential for success in this R&D-focused role.

India, Haryana Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. Efficiency within standard and agreed parameters in preparation of GFT (Gel Feed tank) at GMR. To give output as desired by process requirement abiding to quality requirement. Ensure on time delivery of cleaned GFTs to GMR with set limit of quality specification Ensure the Safety & GMP (Good Manufacturing Practices) in their shifts. Key Responsibilities: Melting Monitor, operate and acknowledge the gelatin melt tank through SCADA (Supervisory Control And Data Acquisition) to prepare melt batch of set specification. Transfer approved gelatin bags to melt tank, dispense material and feed ingredients to melt tank as per procedure and approved gelatin master formula. Operator auto cleaning of melt tanks. GFT Preparation Using weighing booth and dry dye weighing system for dispensing of colors and other ingredients. Generate GFT sheets from the system as per time schedule. Prepare Titanium dioxide slurry batch in Day max & collide mill as per SOP (Standard Operating Practices). Collect gel, trim, purified water and color as per recuperation sheet. Prepare GFTs as per procedure. Documentation of the work done in assigned annexures, as per GDP. VAS (Viscosity Adjustment System) Operate VAS, to set viscosity of GFTs as per viscosity set points. Transfer GFTs from VAS station to HCM area staging station. Documentation of the work done in assigned annexures, as per GDP. Collect sample for check the color through spectrophotometer. To ensure that GFT of set viscosities are delivered to HCM (Head Capsule Machine) area in covered condition within stipulated time. Capsule Trim Grinding Operate Trim grinding machine to grind the capsules and trim. Collect the sample for micro testing from grinded capsules and trims. Documentation of the work done in assigned annexures, as per GDP (Good Documentation Practices). Make sure that the grinded material is placed in assigned racks ( Quarantine or approved) Shift approved grinded material which can be recycled in the same shift. Document environmental conditions. GFT (Gel Feed Tank) & Dish Washing Operate automatic cleaning system to clean GFTs. Manual cleaning of GFT and dishes and deliver the cleaned vessels in time without any delay. Documentation of the work done in assigned annexures, as per GDP. Collection of rinse samples as per schedule/ Test rinse samples. Transfer cleaned and uncleaned vessels (GFTs and dishes). Monitoring the cleaning status and deliver, covered and labelled vessels. Clean other miscellaneous accessories. Collect and classify gel and trim based on their recuperation status, document the same and transfer the material accordingly either to scrap or for recycling. Coordinate with utility and M&E in case of any discrepancy as per the type of problem. Reporting to Shift chemist in case of any discrepancy in the system Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. Reference: R65061

Job Profile - Lab Technical Manager Job Location - Gandhidham, Gujarat CTC - 30k to 40K based on experience and interview. JOB DESCRIPTION: Handling & internal calibration of lab instruments such as Gas Chromatography, UV Spectrophotometer , Karl Fischer , pH meter, Conductivity meter and general lab equipment’s etc.. Minimum One or two times facing of external NABL Audit as per ISO /IEC 17025 : 2017. Testing knowledge of solid fuels (coal , coke) , Animal food & feed ( soya bean meal , rape seed meal etc.) Food & agricultural commodities ( Rice , wheat , Maize, white/Raw sugar) Industrial fine chemicals ( Purity & impurities of Methanol, benzene , Hexane , Toluene, salt etc.) Fertilizer ( Organic & inorganic ) as per ASTM & ISO , FCO test method. Selection , Verification , approval and commissioning of test methods Management and training of staff including that of new appointees and providing guidance to his /her assistants in technical matters. Method Verification , Validation and calculation of uncertainty Measurements and evaluation of test results. Added advantage in the testing mineral ( iron ore , limestone , bauxite , dolomite , Gypsum etc.) Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Schedule: Day shift Work Location: In person

Job Profile - Lab Technical Manager Job Location - Gandhidham, Gujarat CTC - 30k to 40K based on experience and interview. JOB DESCRIPTION: Handling & internal calibration of lab instruments such as Gas Chromatography, UV Spectrophotometer , Karl Fischer , pH meter, Conductivity meter and general lab equipment’s etc.. Minimum One or two times facing of external NABL Audit as per ISO /IEC 17025 : 2017. Testing knowledge of solid fuels (coal , coke) , Animal food & feed ( soya bean meal , rape seed meal etc.) Food & agricultural commodities ( Rice , wheat , Maize, white/Raw sugar) Industrial fine chemicals ( Purity & impurities of Methanol, benzene , Hexane , Toluene, salt etc.) Fertilizer ( Organic & inorganic ) as per ASTM & ISO , FCO test method. Selection , Verification , approval and commissioning of test methods Management and training of staff including that of new appointees and providing guidance to his /her assistants in technical matters. Method Verification , Validation and calculation of uncertainty Measurements and evaluation of test results. Added advantage in the testing mineral ( iron ore , limestone , bauxite , dolomite , Gypsum etc.) Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Schedule: Day shift Work Location: In person

Job Description : Core Technical Skills: Fabric Knowledge: Deep understanding of woven, knit, blended, and natural/synthetic fabrics (cotton, polyester, rayon, etc.) Awareness of fabric behavior during dyeing (shrinkage, color absorption) Dyeing Techniques: Expertise in batch dyeing, continuous dyeing, and garment dyeing Familiarity with reactive, disperse, vat, direct, and acid dyes as per fabric type Shade Matching & Color Management: Practical experience inlab dips, bulk shade approvals, and color fastness testing Use of color matching tools (e.g., spectrophotometer, lightbox, Datacolor) Machine Knowledge: Operation coordination for jet dyeing machines, winch dyeing, soft flow, and HTHP machines Understanding of dyeing machine parameters (temp, time, pressure) Operational & Coordination Skills: Dyeing Recipe Management: Developing and modifying dyeing recipes based on lab trial results Tracking chemical & dye usage, costs, and performance Production Scheduling: Coordinating dyeing batches to align with delivery deadlines Prioritizing orders based on urgency and fabric type Quality Assurance: Ensuring color fastness, uniformity, and defect-free output Coordinating with QA team for inline and final inspections Safety & Compliance: Awareness of chemical handling protocols, MSDS, and EHS guidelines Compliance with GOTS, OEKO-TEX, or other eco standards (if applicable) Soft Skills: Team Coordination: Working closely with dyeing operators, lab technicians, and production heads Training junior staff on dyeing procedures and SOPs Communication: Reporting issues proactively to management Keeping records of dyeing outcomes, complaints, and corrective actions Qualifications & Experience: Education : Diploma/Degree in Textile Processing, Dyeing Technology, or Chemistry Experience : 2+ years in a dyeing unit (preferably with bulk production) Tech Tools : Basic MS Excel, ERP for dyeing/production tracking, color software Job Type: Full-time Pay: ₹35,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person

Urgent Opening for QC Chemist Knowledge of HPLC,GC, Stability , KF,UV, velidation, Documentation etc

Role & responsibilities

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Kra JOB DESCRIPTION To provide routine analytical support to the synthetic team for reaction monitoring by HPLC/GC, analysis of intermediates and API. Perform wet analysis as LOD, IR, Residue on Ignition, KF determination, Titrations etc. Calibration of instruments such as UV, IR, HPLC, GC, Autotitrator, polarimeter etc. LNB writing and all documentation as per 21 CFR compliance. Preparation of required documents for PDR. Skills Required Good communication skills, and effective team player with the ability to work on multiple projects. Robust knowledge of principles, working of applications techniques such as HPLC, GC, Autotitrator, UV spectrophotometer and other laboratory instruments. Qualifications M.sc Analytical chemistry/ M-Pharma About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Show more Show less

Role Summary: The Lab Assistant supports the dyeing laboratory by preparing dye samples, conducting lab dips, maintaining lab records, and ensuring accurate color matching as per customer or production requirements. The role is essential in ensuring quality, consistency, and efficiency in the dyeing process. Key Responsibilities: Prepare lab dips and color samples as per customer requirements or production trials. Assist in recipe formulation and shade matching using spectrophotometer and lab dyeing machines. Weigh dyes and chemicals accurately for lab-scale dyeing. Maintain detailed records of lab dips, dye recipes, and approvals. Coordinate with the production team for recipe scaling and bulk dyeing instructions. Support R&D for new color development or dyeing methods as needed. Skills and Competencies: Basic knowledge of fabric types, dye types (reactive, disperse, vat, etc.), and textile processing. Hands-on experience or training in dye weighing, shade matching, and lab dyeing equipment. Attention to detail and accuracy in color matching and record keeping. Familiarity with color matching software and lab instruments (e.g., spectrophotometer). Good organizational and communication skills. Show more Show less

Job : QA/QC Executive Location: Ode, Ta-Daskroi, Ahmedabad, Gujarat. Department: Quality Assurance / Quality Control Company: Biosurge Healthcare India Private Limited Reporting To : Quality Manager / Head - Quality Department Job Summary : We are seeking a detail-oriented and experienced QA/QC Executive to ensure the highest standards of product quality and compliance with regulatory requirements. The ideal candidate will be responsible for implementing and maintaining QA/QC protocols, conducting inspections, overseeing testing procedures, and collaborating with cross-functional teams to ensure product integrity. Key Responsibilities: Quality Assurance (QA) : Develop, implement, and monitor quality assurance policies and procedures. Conduct internal audits and coordinate external audits (e.g., GMP, ISO). Ensure compliance with SOPs, cGMP guidelines, and applicable regulatory requirements. Review batch manufacturing and batch packaging records. Investigate deviations, non-conformities, and implement CAPA. Conduct training for production and QC staff on quality systems and procedures. Manage change control, document control, and risk assessments. Quality Control (QC) : Conduct sampling, testing, and inspection of raw materials, in-process, and finished products. Operate and maintain lab instruments like HPLC, UV-Vis Spectrophotometer, etc. Ensure accurate documentation of test results as per regulatory standards. Validate and calibrate laboratory equipment periodically. Assist in method development and method validation activities. Coordinate with suppliers and procurement for material quality issues. Required Skills and Qualifications : Bachelor’s/Master’s degree in Pharmacy, Chemistry, or related field. 2–5 years of relevant experience in QA/QC in a pharmaceutical or healthcare manufacturing company. Hands-on experience with analytical techniques and lab instrumentation. Strong documentation, communication, and problem-solving skills. Proficiency in MS Office and quality documentation systems. Benefits Health Insurance: Comprehensive health insurance coverage. Pick and Drop Service: Convenient pick and drop service for employees. Professional Development: Opportunities for professional growth and development. Supportive Work Environment: Collaborative and inclusive workplace culture Kindly share your resume on hr1.rrmgt@gmail.com and contact on 9081819471. Job Type: Full-time Pay: ₹15,000.00 - ₹22,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Beckman Coulter LS Beckman Coulter Life Sciences’ mission is to empower those seeking answers to life’s most important scientific and healthcare questions. With a legacy spanning 80+ years, we have long been a trusted partner to our customers, who are working to transform science and healthcare with the next groundbreaking discovery. As part of our team of more than 2,900 associates across 130 countries, you’ll help drive our vision of accelerating answers—and our commitment to excellence. Beckman Coulter Life Sciences is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. This role will be an On-site role at our Beckman Coulter Life Science, Bangalore Development Center (BDC) manufacturing facility located in Bengaluru. Do you want to work in Manufacturing Operations Team? Do you enjoy working in a dynamic work force, collaborating with other team members and diverse groups, to meet Organization goal and customer demand? Then read on! We are currently seeking a "Polymer Chemist I" position in Production-Operations who will be primarily responsible for polymer dye synthesis and related manufacturing processes. The company is compliant with ISO 9001: 2015, ISO 13485: 2016 & EN ISO 13485: 2016, MDSAP and Beckman Coulter corporate Quality system requirements. In this role, you will be responsible for: Handing metal catalyst reactions. Performing and optimization of C-N and C-C coupling reactions. Experience in handling air/moisture sensitive reagents and performing of reactions at the temperature range of -78ºC to higher temperatures. Perform purification of the organic compounds using different types of column chromatography techniques and other separation techniques. Responsible for organic synthesis of fluorescent dyes suitable for Flow Cytometry applications. The required qualifications for the job include: M.Sc. in Chemistry/Organic Chemistry/Biochemistry or related discipline. Experience: 3-5 years Demonstrate ability to be flexible and resourceful. Ability to work in a team environment & Excellent communication skill. It would be a plus if you also possess previous experience in: Having polymer chemistry and Conjugation chemistry knowledge with good Hands-on experience on HPLC/UPLC/GPC/TFF/Spectrophotometer/Fluorimeter and Automated purification system. This job is eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical insurance to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

We have an urgent vacancy for a QC Executive at Ahmedabad. require a plant QC Executive with hands-on experience in working with chemical plant setup. should have experience in working with chemical plant setup. willing to work during day/Night Shift Required Candidate profile 1. Candidate should have an M.Sc. in (Analytical/organic chemistry). 2. Should have experience in working with chemical plant setups. 3. Should have some experience in QC / QA documentation & SOP.