36 Spectrophotometry Jobs - Page 2

Job Responsibilities: 1. Document analysis procedures and the test results mainly bioburden testing, spectrophotometric testing and mechanical studies using UTM machines 2. Document product stability studies are completed satisfactorily and supported by correct product sample analysis 3. Establish a tracking mechanism for customer & field complaints and suggest corrective actions Profile: 1. You have experience of around 3 or more years in pharmaceutical industry 2. Educational Qualification - M.Sc./M.Pharm degree with strong interest in quality control documentation 3. You work accurately, technically minded and able to work independently after training in the matter entrusted to you. Experience in a formulations/ API industry is an asset

Job Profile for Enzyme Specialist The Enzyme Specialist will be responsible for the research, development, optimization and application of enzymes in various biotechnological, pharmaceutical, agricultural and industrial processes. The role involves enzyme screening, production, purification, characterization and process scaling, with a focus on sustainability and innovation. Qualification & Experience PhD in Biotechnology, Biochemistry, Microbiology, Enzyme Technology or related field. 2–5 years of hands-on experience in enzyme production and application. Strong expertise in molecular biology tools for enzyme engineering (e.g., site-directed mutagenesis, CRISPR, directed evolution). Proficiency in analytical techniques: SDS-PAGE, HPLC, spectrophotometry, LC-MS, etc. Familiarity with bioinformatics tools for enzyme structure-function prediction. Duties & Responsibilities Scope of work includes, but is not limited to the following Design, execute and manage enzyme-related projects, including screening, isolation and production from microbial, plant or synthetic sources. Use molecular cloning, synthetic biology and recombinant DNA technologies to generate optimized gene constructs. Evaluate expression profiles using RT-qPCR, Western blotting or reporter gene assays. Develop and refine methods for enzyme purification, immobilization and stabilization. Characterize enzyme kinetics, substrate specificity, thermostability and pH tolerance. Maintain detailed records and reports for publications, patents, and regulatory compliance. Provide technical support to cross-functional teams and contribute to product development. Key Skills This includes but not limited to the following: Strong analytical and problem-solving abilities. Knowledge of regulatory and safety practices in enzyme handling. Excellent communication and documentation skills. Ability to work independently and in a collaborative environment. Please note that preference will be given to candidates who have relevant research publications, possess knowledge of RT-PCR and are from the northern region. Show more Show less

As a QC Chemist the basic responsiblity will testing raw materials, in-process samples, and finished products for compliance with established specifications. Testing and Analysis: Performing chemical analysis on samples using various techniques (e.g., HPLC, spectrophotometry, titration) to ensure they meet quality standards. Quality Control Procedures: Implementing and following established quality control procedures and protocols. Data Documentation: Recording and analyzing test results, maintaining accurate records, and generating reports. Job Types: Full-time, Fresher Pay: ₹10,753.29 - ₹20,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Schedule: Day shift Evening shift Rotational shift Weekend availability Supplemental Pay: Yearly bonus Work Location: In person

Role Responsibilities: Operate HPLC, ELISA Reader, and microscopy instruments Perform colorimetric and spectrophotometric assays Maintain GLP-compliant documentation and lab practices Support QC testing in biochemical and hematology assays Key Deliverables: Accurate analytical test reports 21 CFR-compliant chromatography data Routine calibration and maintenance logs QC records supporting GMP batch release

Role Responsibilities: Operate HPLC, ELISA Reader, and microscopy instruments Perform colorimetric and spectrophotometric assays Maintain GLP-compliant documentation and lab practices Support QC testing in biochemical and hematology assays Key Deliverables: Accurate analytical test reports 21 CFR-compliant chromatography data Routine calibration and maintenance logs QC records supporting GMP batch release

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. Conferring with scientists and engineers to analyze, interpret, and develop tests. Introducing heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies. Evaluating and ensuring compliance with laboratory safety procedures and standards Job Type: Full-time Pay: ₹14,000.00 - ₹16,000.00 per month Schedule: Day shift Work Location: In person

Job Purpose Plan, coordinate, and direct QC and Application development activities, to support manufacturing and RD in timely delivery of results / products to customers. To ensure analytical / testing protocols are developed for all planned products. Monitoring laboratory data and metrics on a regular basis to ensure that appropriate investigation, corrective action, and/or escalation is conducted. Drive investigation in case of non-conforming laboratory test results. Identify training needs and arrange for training. To ensure adequate testing facility is available at all times. To ensure plan timely calibration / maintenance of all the equipment and instruments. To provide hands on leadership and management of day-to-day quality interactions within the manufacturing group and QC group. Obtain ISO and other specific certifications for the lab. Skills and academic qualifications Functional Skills Functional Skills Required - Lab management Knowledge of battery materials cathode, anode, electrolyte Hands-on experience with assembly and testing of Li ion cells (coin pouch type) Electrochemical methods cyclic voltammetry, impedance spectroscopy, charge / disc Technical Skills required - Inorganic synthesis, especially oxides, phosphates, silicates of alkali and transition metals. Chemical analysis, Thermal analysis, spectrophotometry, etc.

Job title Manager QC Reports to : Plant Head CTC : Salary no bar for deserving candidates Job Description: We are seeking a dedicated and skilled QC Manager for our pharmaceutical manufacturing facility. The ideal candidate will have extensive experience in chemical and instrumental testing, along with in-depth knowledge of pharmaceutical quality control standards. The role will require leadership in overseeing the quality control processes for all types of pharmaceutical products, ensuring compliance with regulatory standards, and maintaining high-quality practices within the lab environment. The QC Manager will be responsible for the testing, calibration, documentation, and preparation of various QC materials, including analytical method validation (AMV), specifications, standard operating procedures (SOPs), and Standard Testing Protocols (STP). The role also requires proficiency in microbiological testing and leadership in managing a team of professionals. Duties and responsibilities: The role would encompass a variety of responsibilities, including and not necessarily limited to the following points: · Chemical and Instrumental Testing : Perform testing using various methods including but not limited to HPLC, FTIR, UV Spectrophotometry, Karl Fischer Titrator, Dissolution, and other chemical and instrumental techniques. · Calibration & Equipment Maintenance : Ensure calibration and proper maintenance of all testing equipment and instruments as per regulatory standards. · Pharmacopeia Adherence : Implement and interpret pharmacopoeia standards for testing and establishing procedures, ensuring compliance with USP, BP, IP, and other relevant pharmacopeia. · Quality Control Documentation : Prepare and review all QC documentation as per the Drugs and Cosmetics Act , New Schedule M , WHO guidelines , and other relevant standards. This includes the preparation of AMV, specifications, SOPs, and STPs. · Regulatory Compliance : Ensure compliance with national and international regulatory requirements such as FDCA , WHO , and MNC guidelines . · Team Management : Lead and train a team of QC analysts and technicians, providing guidance on best practices, troubleshooting, and complex testing. · Microbiological Testing : Oversee and manage microbiological testing, including environmental monitoring, sterility testing, endotoxin testing, and pyrogen testing. · Analytical Method Development : Develop new analytical methods for products not listed in current pharmacopeia. · Inspection and Audit Support : Assist in inspections by regulatory authorities (e.g., FDA , WHO , MNC , TP ) and ensure that the facility meets the required quality standards. · Reporting and Communication : Provide detailed reports on testing results, compliance audits, and other QC activities. Clearly communicate QC issues and resolutions to management and external auditors. Key Requirements: In order to perform your role well, the following qualities will be required: · Educational Qualification : B.Sc., M.Sc., B. Pharm, M. Pharm, or PhD in Pharmaceutical Sciences or Chemistry. · Certifications : FDCA approval for Chemical & Instruments. · Experience : Minimum 15 years of experience in a pharmaceutical quality control department, with at least 5 years in a managerial capacity. Hands-on experience with all types of pharmaceutical formulations, including Tablets, Capsules, Syrups, Ointments, and Liquids. · Testing Expertise : Proficiency in chemical (all types of titration) and instrumental methods (including but not limited to HPLC, UV, FTIR, Karl Fischer Titrator, Dissolution, GC, AAS, etc.). · Documentation Skills : Experience in preparing and reviewing AMV, specifications, STPs, SOPs, and other regulatory documentation. · Microbiological Testing : Basic knowledge of microbiological testing including environmental monitoring, sterility, pyrogen, and toxicity testing. · Regulatory Compliance : In-depth knowledge of Drugs and Cosmetics Act , New Schedule M , WHO guidelines , and other regulatory standards. · Leadership and Training : Ability to handle a team and train others in both technical and analytical skills. · Personal Attributes : Must have a disciplined, compliant, and positive attitude. Strong character, adaptable to changing requirements, and committed to the company’s growth. Good to have skills (not mandatory): · Strong experience in handling FDA , WHO , and MNC inspections. · Ability to work extended hours as required and a flexible attitude toward work demands. · Proficient in ERP systems and familiar with computer-based testing documentation. · Ability to communicate effectively in English (both written and spoken) for internal and external communications, including audits. · Ready to live on the factory campus and demonstrate flexibility as needed. Ideal Candidate Profile: Age: Between 40-50 years . · Demonstrated leadership ability in a QC team and a proactive, solution-oriented approach to problem-solving. · Ready to take on new challenges in a dynamic, fast-paced environment, prioritizing work and the company’s growth. Candidates who wish to apply for the above position may register for interview using the below link/QR code: https://bit.ly/QCManagerMedipol Show more Show less

OPTICS DESIGNER Location Derabassi - Punjab, India Pacesetting. Passionate. Together. HELLA, one of the leading automotive suppliers worldwide, has shaped the industry with innovative lighting systems and vehicle electronics. In addition, the company is one of the most important partners of the aftermarket and independent workshops. What motivates us: Shaping the mobility of tomorrow and fostering the central market trends such as autonomous driving, efficiency and electrification, connectivity and digitization as well as individualization. Every day, 36,000 employees worldwide are committed to this with passion, know-how and innovative strength. YOUR TASKS Design optical systems and components to meet specified requirements by understanding and interpreting customer and project needs. Lead in the development of optical prototypes, perform optical simulations and measurements to verify design performance. Develop optical models with the use of state-of-art software tools such as ZEMAX, FRED, or LightTools. Create optical specifications, tolerances, and manufacturing instructions for new optical products. Collaborate with cross-functional teams including mechanical engineering, manufacturing, and supplier management to ensure optical designs can be produced efficiently and meet quality standards. Provide technical documentation including design review presentations, test reports, and manufacturing instructions. Verify the quality of optical elements and systems with the help of optical metrology techniques including interferometry, spectrophotometry, and imaging metrology. Support the troubleshooting of optical systems in production and post-production, providing technical guidance and expertise. Keep up-to-date with the latest advancements in optics design methodologies, tools, and market trends to improve design capabilities. Execute risk assessments and devise design solutions to mitigate potential product or process issues. Perform design analysis including performance, risk, cost, and manufacturability with appropriate justifications for design choices. Adhere to all safety and compliance procedures in the design, testing, and production phases. YOUR QUALIFICATIONS Oversee and participate in optical testing, calibration, and validation activities. Provide optical design training and mentorship to junior engineers and team members. Participate and contribute to design reviews and improvement meetings. Ensure proper storage and handling of optical components to maintain quality and prevent damage. Assist in procurement of optical components, liaising with suppliers to get the best quality and cost-effective materials. Provide technical support for sales and marketing, such as providing necessary data and documentation for technical presentations or product briefs. Help in troubleshooting and resolving any optical issues identified by customers in a timely manner. Take the opportunity to reveal your potential within a global, family-run company that offers you the best possible conditions for progressing in your career. Please send us your application through our careers portal, citing reference number req16613. HELLA India Lighting Ltd. Neha Saini Derabassi - Punjab

Roles and Responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Coating Design and Development: Design: Utilize optical design software (e.g., TFCalc, Macleod) to design multilayer thin film stacks that meet specific performance requirements (e.g., reflectivity, transmittance, anti-reflection). Material Selection: Choose appropriate materials (e.g., dielectrics, metals) based on optical properties, deposition techniques, and environmental stability. Process Development: D1.evelop and optimize deposition processes (e.g., evaporation, sputtering) to achieve desired film thicknesses, uniformity, and adhesion. Coating Production and Manufacturing: Process Control: Monitor and control coating processes to ensure consistent and high-quality results. Equipment Maintenance: Maintain and troubleshoot coating equipment (e.g., vacuum chambers, deposition sources including Electron beam gun). Production Support: Provide technical support to production personnel to resolve coating-related issues. Characterization and Testing: Metrology: Use optical measurement techniques (e.g., ellipsometry, spectrophotometry) to characterize the optical properties of coatings. Performance Testing: Conduct tests to verify that coatings meet specified performance criteria. Failure Analysis: Investigate and troubleshoot coating failures to identify root causes and implement corrective actions. Research and Development: New Materials and Techniques: Explore and identify new materials and coating techniques to improve performance and expand capabilities. Advanced Coatings: Research and develop advanced coatings for specialized applications (e.g., laser optics, space optics). Project Management and Communication: Project Planning: Plan and manage coating-related projects, including timelines, budgets, and resources. Technical Documentation: Document coating processes, procedures, and test results. Communication: Effectively communicate technical information to colleagues, managers, and customers. Job Types: Full-time, Permanent Pay: ₹36,999.00 - ₹55,208.00 per month Benefits: Leave encashment Provident Fund Schedule: Day shift Application Question(s): What Are the Thin film Coating techniques you know, List atleast 3 Education: Diploma (Required) Location: Puducherry, Puducherry (Preferred) Work Location: In person Application Deadline: 07/05/2025