26 Uvvis Jobs

Role Overview: You will be responsible for providing lipid nanoparticle formulation, characterization, and routine testing support for new product development projects and existing product support. Your role will involve crafting and performing experiments with input from your supervisor, collecting and analyzing experimental data, troubleshooting experiments, and identifying abnormal trends. Additionally, you will support all technical documentation related to projects and product development, collaborate with internal teams, provide technical support to staff and customers, provide training on laboratory/product protocols, and ensure the availability of vital laboratory supplies. Key Respo...

Job Description: You should have a B.Sc or M.Sc academic qualification along with at least 2 years of professional working experience. Additionally, you should have knowledge in Raman, EDXRF, FT-IR, and UV-VIS. Fresh candidates who are interested in working in Gemmology are also encouraged to apply.,

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will be responsible for leading method development, validation, stability studies, and technology transfer activities. Your role will involve collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. Strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement are crucial for success in this position. **Key Responsibilities:** - Develop, optimize, and validate analytical methods such as HPLC, GC, UV-Vis, and Dissolution in accordance with ICH and regulatory guidelines. - ...

You are being sought after to fill the role of a Research Analyst with an M.Sc. Chemistry background to contribute to various activities in the medical device/healthcare manufacturing sector. Your responsibilities will include: - Conducting laboratory testing of raw materials and finished products - Assisting in the development of new products such as adhesives, tapes, laminates, films, coatings, etc. - Performing chemical analysis, physical property tests, and formulation studies - Supporting validation and documentation in compliance with ISO 13485 / MDR - Maintaining lab records, test reports, and ensuring SOP compliance - Collaborating closely with QA, Production, and R&D teams - Trouble...

Role Overview: As a candidate for this position, you will be responsible for developing, validating, and transferring analytical methods for raw materials, intermediates, and finished products in compliance with regulatory guidelines such as ICH, USP, EP, JP, etc. You will utilize techniques including HPLC, UPLC, GC, MS, FTIR, UV-Vis, and dissolution testing for method development. Your role will also involve supporting formulation development by providing analytical data for stability, compatibility, and process optimization studies. Additionally, you will troubleshoot analytical methods and instrumentation to ensure data integrity and reliability. Conducting forced degradation and stabilit...

Role Overview: You will be responsible for developing, validating, and transferring analytical methods for raw materials, intermediates, and finished products in compliance with regulatory guidelines such as ICH, USP, EP, JP, etc. You will perform method development using techniques like HPLC, UPLC, GC, MS, FTIR, UV-Vis, and dissolution testing. Additionally, you will support formulation development by providing analytical data for stability, compatibility, and process optimization studies. Troubleshooting analytical methods and instrumentation to ensure data integrity and reliability will also be a part of your role. Key Responsibilities: - Develop, validate, and transfer analytical methods...

As the Quality Control Head at Celogen Pharma Pvt. Ltd., you will be responsible for directing all laboratory operations related to testing of raw materials, packaging materials, in-process materials, and finished pharmaceutical products. Your role will involve ensuring strict compliance with current Good Laboratory Practices (GLP) and all applicable national and international regulatory standards to provide high-quality, timely analytical support for manufacturing and product release. **Key Responsibilities:** - **Analytical Testing:** - Perform routine and non-routine analytical testing using various techniques such as HPLC, KF, Dissolution, Titration, and Physical testing. - Ensure testin...

As a Leachables & Extractables (L&E) Analyst at Anazeal Analytical & Research Pvt. Ltd., located in Navi Mumbai, Maharashtra, you will be responsible for performing analytical testing and characterization of extractables and leachables in pharmaceutical containers, closures, and medical devices. Your role will involve method development, validation, and data interpretation in compliance with regulatory guidelines such as USP, ISO, and ICH. Key Responsibilities: - Perform Extractables and Leachables studies for pharmaceutical packaging materials, process equipment, and medical devices. - Conduct sample preparation, extraction, and analysis using analytical instruments such as GC-MS, LC-MS, IC...

As a Research Associate at our company, you will be part of a dynamic research team passionate about scientific research and laboratory work. Your role will involve conducting and assisting in laboratory experiments, performing synthesis, purification, and analysis of compounds, maintaining detailed experimental records, and supporting ongoing research projects while ensuring lab safety. Key Responsibilities: - Conduct and assist in laboratory experiments - Perform synthesis, purification, and analysis of compounds - Maintain detailed experimental records - Support ongoing research projects and ensure lab safety Qualifications Required: - M.Sc. in Chemistry (Organic Chemistry) - Strong found...

Role Overview: As the QC Head, you will be responsible for leading the Quality Control function in medical device manufacturing to ensure that products meet global regulatory, safety, and performance standards. Your role will involve overseeing raw material testing, in-process quality checks, stability studies, validation protocols, and final product release in compliance with applicable regulatory guidelines. Key Responsibilities: - Establish, implement, and maintain QC protocols, SOPs, testing procedures, and specifications. - Ensure batch-wise testing, documentation, and release of raw materials, intermediates, and finished products. - Oversee microbiological and biochemical testing for s...

As the Lead of the Residue Analysis & Instrumentation section in the laboratory, your role involves overseeing and managing the analysis of pesticides, antibiotics, veterinary drugs, mycotoxins, heavy metals, and other contaminants in food samples. You will be responsible for operating, supervising, and maintaining advanced analytical instruments such as LC-MS/MS, GC-MS/MS, ICP-MS / ICP-OES, HPLC, GC, AAS, UV-Vis, and FTIR. Your duties include ensuring compliance with NABL (ISO/IEC 17025:2017), FSSAI guidelines, Codex, and BIS standards. You will also be involved in method validation, verification, calibration, and measurement of uncertainty. Reviewing and authorizing test reports as an Auth...

As a Quality Control Chemist, you will be responsible for ensuring the quality of products through various testing methods and procedures. You will play a crucial role in maintaining high standards of quality control to meet regulatory requirements and customer expectations. - Perform quality control tests on raw materials, intermediates, and finished products using analytical techniques such as HPLC, GC, UV-Vis, and FTIR. - Record and analyze test results, and report any deviations from specifications to the appropriate personnel. - Maintain accurate documentation of all test results and ensure compliance with standard operating procedures (SOPs) and Good Laboratory Practices (GLP). - Inves...

As a Chemical Process Development Engineer, you will play a crucial role in leading the development and optimization of chemical processes using various flow reactors like microreactors, tubular reactors, and packed-bed reactors. Your responsibilities will include: - Collaborating with synthetic chemists and process engineers to transition batch processes to continuous flow - Developing and validating process parameters such as residence time, flow rates, mixing, pressure, and temperature - Integrating online/inline monitoring tools (PAT) including FTIR, UV-Vis, NMR, and HPLC - Ensuring robust data analysis, modeling, and documentation of experiments and findings Qualifications Required: - B...

As a member of the Analytical Development team at our clinical-stage vaccine innovation company, your primary responsibility will be to support the developmental activities in the laboratory. You will have the opportunity to assist in the design, execution, and interpretation of experiments to analyze drug substances and intermediates, including proteins and carbohydrates. Your key responsibilities will include: - Performing microplate assays, including enzymatic assays - Utilizing HPLC techniques, especially SEC and RP-HPLC with experience in Chemstation - Working with CE and iCIEF, especially with Protein Simple or PA-800 systems - Assisting in analytical method development of new assays -...

Role Overview: Join a team with a more than 70-year history of discovery, determination, and innovation at Pall Corporation, a global leader in high-tech filtration, separation, and purification. Your role will involve providing lipid nanoparticle formulation, characterization, and routine testing support for new product development projects and existing product support. You will collaborate with internal teams to ensure successful project completion and provide technical support to staff and customers as needed. Key Responsibilities: - Craft and perform experiments with input from supervisor - Collect and analyze experimental data, present findings, and outline future plans - Troubleshoot e...

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will play a crucial role in leading method development, validation, stability studies, and technology transfer activities. Your meticulous nature and extensive experience will be essential in collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. You should possess strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement. - Developing, optimizing, and validating analytical methods such as HPLC, GC, UV-Vis, and Dissolution according to ICH and regulatory guidelines....

As a Validation Specialist at our company, your primary responsibility will be to plan, execute, and document analytical method validation activities for raw materials, in-process samples, finished products, and cleaning validation. This will involve assessing various parameters like accuracy, precision, specificity, linearity, robustness, LOD/LOQ, and others. You will also review and approve validation protocols and reports to ensure compliance with ICH Q2(R1), USP, and other regulatory standards, maintaining adherence to GMP, GLP, and cGMP guidelines. Your role will require collaboration with R&D, QA, and Production teams to facilitate seamless tech transfer and validation support. Trouble...

Role Overview: As a Research Scientist in this role, you will be responsible for synthesizing and immobilizing photocatalysts for solar hydrogen production. You will conduct material characterization using techniques such as XRD, SEM, TEM, FTIR, UV-Vis, etc., and analyze the related data through Python coding, theory, and simulations. Your primary duties will involve designing and executing experiments focused on solar-driven water splitting. You will be tasked with optimizing reaction conditions and analyzing performance metrics to enhance efficiency. Furthermore, you will leverage your programming skills in Python, Artificial Intelligence (AI), and Machine Learning (ML) for data processing...

As a Pharma Subject Matter Expert (SME) Trainer, you will be responsible for training candidates in various aspects of Quality Control (QC), Cell Culture Techniques, and Laboratory Procedures. Your role involves providing hands-on experience in analytical testing, microbiological testing, and pharmaceutical laboratory operations. It is essential to educate candidates on method validation, stability testing, and data integrity while ensuring compliance with FDA, USP, and cGMP regulations. Additionally, you will train individuals in utilizing HPLC, GC, UV-Vis, FTIR, PCR, ELISA, and Spectroscopy techniques. Your responsibilities include conducting mock interviews, assisting with resume preparat...

The QC Analyst II position at Piramal Pharma Solutions involves performing analytical chemistry examination testing on raw materials, finished products, or stability samples following approved Standard Operating Procedures (SOPs) and valid methods. This role, which operates during 2nd shift hours, is crucial for ensuring product quality and compliance with regulatory standards. Key responsibilities of the QC Analyst II include conducting chemical or physical testing analysis, documenting and submitting all raw data and results in LIMS, preparing reagents for chemical analysis, and ensuring compliance with compendial (USP/EU) testing requirements as per FDA 21 CFR. Moreover, the incumbent is ...

As a potential candidate for this position, you should possess an academic qualification of B.Sc or M.Sc. Additionally, a professional qualification of 2 years or more working experience is required. It is essential to have knowledge in Raman, EDXRF, FT-IR, and UV-VIS. Fresh candidates who are eager to work in Gemmology are also encouraged to apply.,

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will play a crucial role in leading method development, validation, stability studies, and technology transfer activities. Your meticulous nature and extensive experience will be essential in collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. You should possess strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement. Your responsibilities will include developing, optimizing, and validating analytical methods such as HPLC, GC, UV-Vis, and Dissolution according ...

You will be responsible for planning, executing, and documenting analytical method validation activities for raw materials, in-process samples, finished products, and cleaning validation. This includes assessing accuracy, precision, specificity, linearity, robustness, LOD/LOQ, and other parameters. You will review and approve validation protocols and reports in accordance with ICH Q2(R1), USP, and other regulatory standards to ensure compliance. Your role involves ensuring that all analytical method validation (AMV) activities adhere to GMP, GLP, and cGMP guidelines. Collaboration with R&D, QA, and Production teams is essential for seamless tech transfer and validation support. You will trou...

As a Research Scientist in this role, you will be responsible for synthesizing and immobilizing photocatalysts for solar hydrogen production. You will conduct material characterization using techniques such as XRD, SEM, TEM, FTIR, UV-Vis, etc., and analyze the related data through Python coding, theory, and simulations. Your primary duties will involve designing and executing experiments focused on solar-driven water splitting. You will be tasked with optimizing reaction conditions and analyzing performance metrics to enhance efficiency. Furthermore, you will leverage your programming skills in Python, Artificial Intelligence (AI), and Machine Learning (ML) for data processing, reaction kine...

As a Research Scientist in the field of photocatalysis for solar hydrogen production, your primary responsibility will be to synthesize and immobilize photocatalysts. You will be required to conduct material characterization using techniques such as XRD, SEM, TEM, FTIR, UV-Vis, etc., followed by data analysis utilizing Python coding, theory, and simulations. Furthermore, you will be tasked with designing and executing experiments related to solar-driven water splitting. Your role will involve optimizing reaction conditions and analyzing performance metrics to enhance the efficiency of the process. Your proficiency in programming, particularly in Python, AI, and Machine Learning, will be esse...