165 Spectrophotometer Jobs - Page 5

Jairamdass Khushiram have two herbal manufacturing units JK Botanicals Pvt. Ltd (Processing Unit) and SA Herbal Bioactives LLP (Extraction Unit),which are globally certified units with BRCGS , ISO, GMP, Kosher, Halal & Organic Certification Website - https://www.jairamdass.com/ Company Video :- https://youtu.be/SnDkfko3Cgs Qualification - BSc/B.Tech/ MSc in Lifesciences/ Botany/ Biotechnology/ Food Technology/Microbiology/ Chemistry Job location - Plot No. – M 14, Taloja MIDC Industrial Area Dist. – Raigad, Maharashtra 410208, Tondare Phata stop Post - QC Executive Job Profile :- Analytical Testing & Analysis: RM Analysis report. In-Process product analysis Reports Preparation reports for RM & FG Chemicals inventory management of Hot lab & Wet Lab HPLC UV spectrophotometer Colorimeter TLC Also have a knowledge of wet lab analysis like titrations, extractions, layer separations, gravimetric analysis, etc If interested please share your updated resume on hr@jairamdass.com Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Work Location: In person

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

Key Responsibilities:Conduct physical and chemical testing of raw oil, refined oil, and final tray oil products. Perform routine analysis such as viscosity, density, acid value, moisture content, FFA (Free Fatty Acids), and other parameters. Calibrate and operate lab instruments such as GC (Gas Chromatograph), pH meter, Karl Fischer, Spectrophotometer, etc. Maintain proper documentation of test results and report deviations to the Quality Manager. Collect and retain production samples as per standard operating procedures (SOPs). Ensure all lab work complies with ISO, FSSAI, BIS, or other applicable standards. Maintain cleanliness and safety of lab equipment and environment. Assist in validation, shelf-life studies, and R&D trials for new oil formulations. Communicate with the production team to suggest corrections or improvements in process quality. Conduct inspections of packaging materials like tray seals, oils filled, and batch labelling. Participate in audits, internal reviews, and continual improvement activities.

• Knowledge of acid-base titration, sulphonation reaction testing, active matter content. • ability to operate standard lab instruments, pH meter, handling wet lab procedures • willing to learn: GC, HPLC, spectrophotometer, viscometer, etc.

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 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 5 - 8 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 Title: Textile Application Specialist (Manager/Sr. Manager) Location: Chennai Department: Textile Application Lab Reports To: Head – R&D/QC/NPD Type: Contract Job Summary: Seeking a Textile Application Specialist to support formulation testing and development. The role includes lab trials, data reporting, and coordination with R&D and marketing teams. Key Responsibilities: Conduct textile processing trials (Scouring, Bleaching, Soaping, Dyeing, Printing, Finishing). Operate lab instruments (HPLC, spectrophotometer, pH meter, etc.). Perform titrations, standard solution prep, and calibration. Collaborate with marketing on troubleshooting experiments. Maintain test records and prepare summary reports. Thorough knowledge of pulp and processing lab equipment. Qualifications: BE/B.Tech or Diploma in Textile Chemistry / Fashion Technology. 7+ years’ experience or fresher from a reputed textile institute. Strong knowledge of textile chemicals and lab procedures. Good communication, documentation, and teamwork skills. Show more Show less

Tips: Provide a summary of the role, what success in the position looks like, and how this role fits into the organization overall. Responsibilities Perform a part of Research in Anaerobic microbial cultivation documentation and data analysis Antimicrobial activity for a specific compound against the given microbes and documentation of the same Qualifications UG or PG Students who are studying currently and know the basic microbiological technique like serial dilution, plating, antimicrobial activities and UV spectrophotometer No. of Post 2 Period of internship 1 month (June 17, 2025- July 15, 2025) Stipend Rs. 3000/- Location K.S.Rangasamy College of Technology, Tiruchengode Certification DPIIT recognized Company certification Show more Show less

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 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

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 the 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 2" 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: Experience in handing metal catalyst reactions. Experience in 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. Having polymer chemistry and Conjugation chemistry knowledge with good Hands-on experience on HPLC/UPLC/GPC/TFF/Spectrophotometer/Fluorimeter and Automated purification system. The required qualifications for the job include: M.Sc. in Chemistry/Organic Chemistry/Polymer chemistry/Biochemistry or related discipline, with minimum of 5+ year’s industrial experience. Demonstrated ability to be flexible and resourceful. Ability to work in a team environment & Excellent communication skill. Previous experience with polymer chemistry and protein conjugation will have an added advantage. It would be a plus if you also possess previous experience in: Organic synthesis of fluorescent dyes suitable for Flow Cytometry applications. 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

Location: Kurali, Karjan, Vadodara Qualification: B.Sc or M.Sc. Chemistry (Analytical chemistry/Inorganic chemistry) or Bachelor's in Food Technology or Food Science or Certified Food analyst by FSSAI. Experience: Should have 1 to 2 Years’ Experience in Analysis of Food from reputed Lab or Food industry. Experience in Analysis of Spices & related products may prefer. Reporting To: Manager Quality Area of Operations: Quality (QA/QC) Key Responsibilities 1. To Analyse and Manage overall Laboratory Testing & related Compliances. 2. To Manage the Samples of Raw materials, Packaging Materials, Semi finished, Finished Goods & R&D Which Provided for Testing. and Provide Results on time and Co Ordinate with the team for acceptance or rejection/On time Clearance. 3. To maintained all the Documentation related to Analysis & Laboratory. Must be Maintained the Stock of all the Laboratory Items and their Consumption on time with records. 4. To Store all the Retention & Controlled Samples as per the requirements and Maintain their records. 5. Responsible to do in house Calibration, Verification & Validation of Laboratory Items with proper Documentation as per the Std. Requirement. Should be able to coordinate for preventive maintenance for lab instruments. 6. Responsible to Maintain and Implementation of GHP, GLP, 5S and other Good Practices/Presentations in Laboratory. Should have knowledge of Good Laboratory Practices, NABL standard & FSSAI standards. 7. Responsible to Intimate any purchase or out of stock Lab. Items before 1 or 1.5 Month to the Reporting Manager wisely. 8. To maintain all the External lab. Test Reports and making of Certificate of Analysis on time. And Intimate before due date to next External test required. 9. Should be able to do Standardization of Prepared Chemicals to Check their Efficiency & Record keeping. 10. Able to Provide the basic Food safety/Chemical safety related Trainings to the Work Force. As & When Required. 11. Responsible to take care of all Glasswares, Instruments & Chemicals in Lab. To Avoid any Wastage/Breakage and has to be Maintained all time Safe Work Place in Laboratory. 12. Required hand on Experience to operate Moisture analyser, Hot air oven, Soxhlet apparatus, pH Meter, Titration, Centrifuge, Muffle furnace, BD meter, Sieve shaker, UV-Vis Spectrophotometer, Incubator, LAF, Autoclave, weigh balance, Dessicator, Mixture etc. 13. Should have good Computer skills (able to work on ERP system as & when required), Good Analytical skills with Accuracy. 14. Daily Reporting to the Quality Manager. Follow the Instructions form Reporting Manager and play supportive roll. Must be followed the Company's Rules and Regulations. Flexible to work in rotational shift. Ready to adopt any task/work from superior as & when required. Job Types: Full-time, Permanent Pay: ₹240,000.00 - ₹300,000.00 per year Education: Bachelor's (Preferred) Work Location: In person

We are looking for a skilled and experienced Microbiologist with 2–5 years of hands-on experience in microbiological processes, media optimization, and bioreactor handling. The ideal candidate will support R&D or QC functions in fermentation, strain maintenance, microbial analysis, and yield optimization for industrial and cosmetic applications. Key Responsibilities: Design and optimize culture media for microbial growth and product yield enhancement. Operate and monitor bench-top/lab-scale bioreactors for fermentation processes. Perform sub-culturing, strain preservation, and microbial storage (slant, glycerol stock, etc.). Calibrate lab instruments (e.g., pH meter, autoclave, incubator, spectrophotometer). Conduct biomass/yield analysis through gravimetric or spectrophotometric methods. Perform MLT for raw materials, in-process samples, and final products. Analyze purified water, RO water, and microbiological quality of water samples. Maintain detailed records of test procedures, observations, and results. Ensure proper aseptic handling, sterilization, and biosafety measures. Qualifications: Education: M.Sc. in Microbiology (mandatory) Experience: 2–5 years of relevant lab experience in fermentation, cosmetics, pharmaceuticals, or food industries. Key Skills: Strong knowledge of microbiological techniques and strain maintenance. Experience in handling fermentation processes and yield analysis. Expertise in lab equipment calibration and troubleshooting. Familiarity with water analysis, MLT, and standard microbiological testing. Good documentation and observation skills; ability to follow SOPs. Basic understanding of GLP/GMP and laboratory safety norms. Preferred Experience: Exposure to downstream processing (e.g., centrifugation, filtration). Experience in cosmetic ingredient fermentation or biopolymer production. Knowledge of microbial screening and strain improvement techniques. Salary & Benefits: Salary: As per industry standards Joining: Immediate or within 30 days preferred Show more Show less

Perform chemical, physical, and instrumental analyses of raw materials, in-process samples, and finished products. Prepare reagents, standard solutions, and samples for testing as per established protocols Operate, calibrate, and maintain laboratory.

Perform chemical, physical, and instrumental analyses of raw materials, in-process samples, and finished products. Prepare reagents, standard solutions, and samples for testing as per established protocols Operate, calibrate, and maintain laboratory.

We are hiring an MSc/Postgraduate professional in Microbiology/Chemistry/Product Development for our Faridabad-based team! Key Responsibilities: 1. Conduct microbiological & chemical analysis of raw materials, in-process, and finished products. 2. Perform microbial testing (e.g., TVC, pathogens), media prep, and aseptic sampling. 3. Support new product development, improve formulations & perform stability, efficacy & shelf-life studies. 4. Maintain lab records, perform data logging (LIMS), statistical analysis & reporting. 5. Ensure QC/QA compliance with ISO, GMP, GLP; troubleshoot lab issues. 6. Operate & maintain lab instruments (pH meter, spectrophotometer, autoclave, etc.). 7. Follow lab safety & regulatory protocols; manage waste disposal. 8. Stay updated with research trends & share knowledge. ✅ Requirements: 1. MSc in Microbiology/Chemistry/Biotech/Biochem with 1+ yrs experience 2. Strong lab skills, product development exposure, and data analysis proficiency Location: Faridabad Apply now: vikas@triindia.org Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹30,000.00 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Fixed shift Weekend availability Work Location: In person

ETP/RO/MEE/WTP Chemist - Chemical Manufacturing Company Job Title: ETP/RO/MEE/WTP Chemist Department: Environment, Health & Safety (EHS) / Utilities Industry: Chemical Manufacturing Job Summary: The ETP/RO/MEE/WTP Chemist is responsible for the efficient operation, monitoring, and maintenance of effluent treatment systems including the Effluent Treatment Plant (ETP), Reverse Osmosis (RO) plant, Multiple Effect Evaporator (MEE), and Water Treatment Plant (WTP). The role ensures compliance with environmental norms and supports sustainable water management practices. Key Responsibilities: Operate, monitor, and maintain the ETP, RO, MEE, and WTP systems as per standard operating procedures. Conduct chemical analysis and water quality testing of influent, effluent, treated water, and sludge. Monitor and maintain pH, TDS, COD, BOD, MLSS , and other key parameters regularly. Ensure optimal dosing of chemicals and adjust process parameters accordingly. Maintain proper records/logbooks for water analysis, plant operations, and chemical consumption. Conduct daily inspection of treatment units and identify faults or maintenance needs. Liaise with the maintenance team for troubleshooting and servicing of pumps, valves, and other mechanical/electrical components. Ensure compliance with pollution control board (PCB) norms and assist in documentation for audits and inspections. Maintain good housekeeping and ensure adherence to safety protocols in the plant. Handle safe storage and usage of treatment chemicals like lime, alum, PAC, polyelectrolytes, etc. Key Skills & Competencies: Sound knowledge of effluent/water treatment processes and environmental standards Familiar with analytical instruments like pH meter, TDS meter, spectrophotometer, etc. Understanding of hazardous waste handling & disposal norms Proficient in record keeping and reporting Strong problem-solving and decision-making skills Ability to work independently and in shift operations Qualification & Experience: Education: B.Sc. / M.Sc. in Chemistry, Environmental Science, or relevant discipline Experience: 2 to 6 years in ETP/RO/MEE/WTP operations in a chemical or allied manufacturing industry Share me your updated resume - 8989837901(Whatsapp) Job Type: Full-time Pay: ₹300,000.00 - ₹500,000.00 per year Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Executive Date: May 18, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Primary Responsibilities: Analytical Method development for API/NCE sample. Analysis of raw material, Intermediate, API/NCE samples on gas chromatography, liquid chromatography and chemical analysis. Method validation for API/NCE purity, impurity, excipients methods. Trouble shooting of various analytical issues for various products. Maintenance, calibration & trouble shooting of HPLC and GC. Preparation of SOP for related to instrument and system. Method transfer and method demonstration at other location as and when required. Documentation like ATP, Development report, Validation protocol, Validation report, STP preparation. To work as per cGMP/OECD GLP and to ensure its compliance. Basic understanding of ICH guidelines Candidate should have basic knowledge about handling of instruments like UV visible spectrophotometer High-performance liquid chromatography Ultra-performance liquid chromatography Karl-Fischer Titration Differential scanning calorimetry USP Dissolution Apparatus I and II Other minor equipment like analytical balance, pH meter, Sonicator and microcentrifuge. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Overview THE ROLE: The Chemist will perform standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. How You Would Contribute Perform laboratory testing including qualitative and quantitative chemical and physical analysis of raw materials, finished products, and stability samples. Prepare standards and reagents; calibrate and operate sophisticated laboratory instrumentation such as HPLC, FTIR, UV-Visible spectrophotometer. Review product certificates of analysis for accuracy and conformance, maintaining Certificates of Analysis (C of A) files. Perform routine calibration and performance verification of lab equipment and instrumentation. Provide input on Standard Operating Procedures (SOPs), Test Methods, and laboratory documents. Participate in investigations, address Out of Specifications (OOS), resolve deviations, and implement CAPA with general supervision. Adhering strictly to current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP), detailing data in lab notebooks and following cGMP guidelines. Interpret test results, comparing with determined standards and limits, and analyze records for trend verification under supervision. Maintain a safe, clean, and efficient laboratory environment. Supervisory Responsibilities None Ability to adapt as the external environment and organization evolve. Skills And Background Required To Be Successful Ability to complete testing according to established methods. Demonstrates basic proficiency in lab instrumentation and multiple test methods. Ability to solve problems and carry out responsibilities under supervision. Ability to coordinate workload for effective implementation. Strong customer and results orientation. Ability to interact effectively at all levels with sensitivity to diversity. Ability to function as team member. Education Bachelor/Master of Science in Chemistry, Biochemistry, or related scientific fields, or equivalent experience. Knowledge of LC/MS and GC/MS. Previous cGMP regulation and compliance knowledge. Nutraceutical or pharmaceutical laboratory work experience. Knowledge in ISO17025 Lab Management. Join us in this outstanding opportunity to contribute to world-class research and help craft the future of nutritional science! Terms of Use Privacy Policy Compliance Documents CSR Policy Show more Show less

Objectives Of The Position Plan and execute regional, global, internal and customer oriented projects in the lab Schedule lab application activities and organize work to meet study requirements in a timely, cost effective manner Develop, coordinate, manage all technical activities such as customer projects and Application projects Drive the activities of the Application laboratory to complete the assigned regional / global customers projects in the stipulated timelines, in order to enhance the output of the lab. Support sales and technical services team to build strong new business development pipeline, as well as achieve growth and profitability targets in line with ENP strategy Application Lab Support Main Areas of Responsibilities and Key Activities: Proposing and coordinating Application projects for products to develop data for customer solutions in conjunction with regional and global technical service and business development To work on product applications in formulation Development of various dosage forms such as Tablets, Oral liquids, Oral powders and Capsule for customer projects Design and execute experiments to develop new formulations, including solid orals, liquid and topical products, that utilize BASF’s excipients. Work on advanced technologies such as hot melt extrusion, spray drying and other novel concepts to support internal and customer product developments Optimize existing formulations by assessing the functionality and effectiveness of excipients in enhancing the performance and stability of the final product Conduct pre-formulation studies and stability testing of the developed formulations Analytical Testing Conduct analytical characterization of formulations and excipients, in accordance to standard pharmacopeal and in house testing procedures Utilize techniques such as HPLC, UV spectrophotometer, Dissolution testing, Rheometer etc. to characterize excipeints and the formulations Customer Support Develop deep and trusting customer relationships that ensure access to growth opportunities Provide complete and timely support to internal and external customers on Product Application matters, including prototypes, lab trials and trials at customers end in South Asia Assist in troubleshooting formulation challenges and provide solutions to enhance product quality through support in the lab as well as at the customer site as required. Documentation And Reporting Prepare detailed reports and presentations on experimental findings, including formulation development and analytical results Monthly technical reports Maintain accurate and organized laboratory records in compliance with company and regulatory standards. Project Activities Projects for Existing and New Product Launches Participation in product development teams Initiate and manage projects in raising brand awareness including working with Universities or External associations Support various communication programs in the country such as seminars, workshops and promotion programs. Adapt materials to meet local promotion needs and understanding ;improve effectiveness of presentation of technical information to customers. Collaboration Work closely with cross-functional teams, including technical services, sales, regulatory affairs, quality and marketing, to support product development and launch activities. Drive the collaboration activiteis with the identified parterners Participate in customer meetings, providing insights on excipient applications and formulation strategies Prepare for lab audits, work closely with lab team and other interdisciplinary team members Training And Mentoring Provide training and guidance to laboratory interns and laboratory technicians as needed. Identify the areas of improvement and communication to the team Safety Foster a culture of safety and compliance within the laboratory environment. Job Skills Formulation research and development Innovation Ability to contribute individually, yet demonstrating team spirit Updated on recent formulation trends Technical presentation skills Good communication skills Job Requirements Minimum master’s degree in pharmacy (Pharmaceutics) / PhD preferred More than 5 years of formulation experience from the pharmaceutical industry (hands-on experience to develop various pharmaceutical dosage forms) and excipient industry. Prefers to have candidates who has additionally worked on the analytical developments Development of Oral solid dosage forms such as Immediate release, Modified release and delayed release formulations Development of topical and parenteral formulations and experience handling of analytical instruments such as HPLC, UV and dissolution testing will have advantage Sound knowledge about technology transfer activities and experience in the scale up/ commercialization of formulations Good documentation practices, maintenance of lab internal documents, such as SOPs, risk assessment documents Knowledge in handling technical matters and commercial transactions; knowledge and / or skills in pharmaceutical technology and operations; being familiar with pharma related quality standards (GMP) preferable; ideally, experience in key account management Good and sound R&D knowledge in Pharmaceutical Industry, product life cycle management and high level of presentation skills Show more Show less

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

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