8 Uvvis Jobs

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 preparation, and providing real-world project training to enhance the skills of the candidates. You will be required to ensure that trainees understand deviation handling, OOS/OOT investigations, CAPA processes, and regulatory audit procedures. Collaboration with the sales team is crucial to ensure that the trainees meet the expectations of their future employers. The ideal candidate should possess hands-on experience in cell culture, microbiology, and analytical laboratory techniques. Proficiency in HPLC, GC, FTIR, UV-Vis, and PCR is essential for this role. A strong understanding of data integrity, compliance documentation, and industry regulations such as cGMP, ICH, USP, and FDA guidelines is also required. Previous experience in stability testing, method validation, and impurity profiling will be beneficial. Your excellent mentoring and training skills, coupled with a passion for upskilling candidates, will be key to your success in this position. In addition to the specific responsibilities mentioned above, you will be expected to conduct one-on-one in-person training sessions, coordinate with internal teams for seamless training execution, and provide support to candidates in resume building, interview preparation, and exposure to real-time projects. Keeping abreast of industry trends and continuously updating training content accordingly is an integral part of this role. Please note that candidates who successfully complete two years with us will be eligible for visa sponsorship. If you are enthusiastic about mentoring and developing future pharmaceutical professionals, we look forward to receiving your application.,

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 expected to possess a good understanding of laboratory safety practices, cGMP, good documentation practices, and compendial testing requirements. The ideal candidate for this role should hold a Bachelor's degree in chemistry, biology, microbiology, or a related science field with relevant laboratory coursework. Additionally, a minimum of 2 years of laboratory experience, preferably in a GMP environment, is required. Proficiency in a range of analytical techniques such as Wet Chemistry testing, Balance, Dissolution, FTIR, KFM, UV/Vis, Titrations, Viscosity, PSD testing, pH, and conductivity is essential. The successful candidate should demonstrate strong written, verbal, and interpersonal communication skills, as well as proficiency with computer software like MS Word, Excel, or PowerPoint. As part of the Piramal Group, Piramal Pharma Solutions is committed to inclusive growth, ethical practices, and equal employment opportunity, ensuring that all applicants and employees are treated fairly in all personnel matters. 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. With a global network of facilities, PPS provides services ranging from drug discovery solutions to commercial supply of APIs and finished dosage forms. The organization's expertise covers a wide range of technologies, making it a preferred partner for innovators and generic companies worldwide. If you are passionate about quality control and analytical chemistry, and meet the qualifications mentioned above, we encourage you to apply for the QC Analyst II position at Piramal Pharma Solutions.,

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 to ICH and regulatory guidelines. You will be responsible for preparing and maintaining validation protocols, analytical reports, and ensuring compliance with Good Documentation Practices (GDP). Additionally, you will oversee method transfer to QC, provide training, and address any troubleshooting issues that may arise. Conducting stability studies, preparing data reports, and collaborating with cross-functional teams to support product development will also be part of your role. Furthermore, you will be expected to investigate and resolve analytical issues, including OOS, OOT, and deviations, and implement Corrective and Preventive Actions (CAPAs) as necessary. Maintaining up-to-date documentation and ensuring compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) will be integral to your responsibilities. You will also evaluate vendors and key starting materials (KSMs) and provide insights to management based on your findings. In terms of past experience, you should have a strong understanding of analytical chemistry principles and techniques, including HPLC, GC, Dissolution, and UV-Vis. Proven experience in method development, validation, and regulatory compliance is crucial for this role. Familiarity with global pharmaceutical regulations such as those from the FDA, EMA, WHO, and ICH guidelines is essential. You should also be skilled in handling regulatory submissions and documentation, possess excellent problem-solving abilities, and have experience mentoring R&D scientists. Familiarity with CAPA systems and good documentation practices will further strengthen your candidacy for this position.,

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 troubleshoot analytical method issues, propose enhancements, and recommend revalidations as needed. Maintenance and calibration of analytical instruments such as HPLC, GC, UV-Vis, and FTIR will be part of your responsibilities. In preparation for regulatory inspections and internal audits, you will participate in these processes. Additionally, you will play a key role in training and guiding junior QC staff on method validation procedures and regulatory expectations. It is crucial to ensure the completeness, accuracy, and proper archiving of all documentation as per standard operating procedures (SOPs). This position is based in Giloth, Neemrana, Rajasthan, and requires prior experience in a similar role. The job is full-time and permanent, offering benefits such as commuter assistance and provided meals. The work schedule is during day shifts with a yearly bonus component. The role necessitates on-site presence for work. If you meet the experience requirements and are adept at analytical method validation within a regulated environment, we invite you to apply for this challenging opportunity.,

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 kinetics modeling, and applying AI/ML techniques in catalysis research. In addition to your technical responsibilities, you will be expected to maintain detailed research records, prepare reports and publications, and contribute to project presentations and proposal drafting. Joining the team at India's leading not-for-profit private university will give you the opportunity to be part of a global institution with a strong emphasis on research and innovation.,

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 essential for data processing, reaction kinetics modeling, and the application of AI/ML techniques in catalysis research. In addition to your technical responsibilities, you will be expected to maintain detailed research records, prepare reports and publications, and contribute to project presentations and proposal drafting. Joining our team at India's leading not-for-profit private university will offer you a global platform to engage in cutting-edge research and innovation, contributing to our strong foundation in research excellence.,

The main responsibilities for this role include synthesizing and immobilizing photocatalysts for solar hydrogen production, conducting advanced material characterization using techniques such as XRD, SEM, TEM, FTIR, UV-Vis, etc., and performing advanced simulations. You will be responsible for designing and executing experiments related to solar-driven water splitting, optimizing reaction conditions, and analyzing performance metrics. Additionally, you will be required to utilize programming skills in Python/AI/ML for data processing, reaction kinetics modeling, and AI/ML applications in catalysis. It is important to maintain detailed research records, write reports/publications, and contribute to project presentations & proposal drafting. The company offering this position is India's number one not-for-profit private university with a global presence and a strong foundation in research and innovation.,