4 Uvvis Spectroscopy Jobs

As a Chemical Research Scientist C in the R&D Department in Bangalore, your role involves conducting literature search and review using basic software knowledge like Sci-Finder, Chem-draw, and other databases. You will also need to have a basic understanding of AI & Chat GPT. Your responsibilities include: - Executing synthesis and scale up of small organic molecules/intermediates, active ingredient/polymers/dispersions to multi-kilogram quantities under the supervision of the department head, adapting to evolving project requirements. - Employing techniques such as column chromatography, recrystallization, fractional, column & vacuum distillation, and different techniques. - Utilizing HPLC, GC, TLC, NMR, IR, and UV-Vis spectroscopy for compound analysis and interpretation of chemical structure. - Assisting in the preparation of reports and research publications. - Maintaining accurate records of experiments, observation sheets, including reports, presentations, protocols, and publications. - Developing detailed plans outlining the purpose, materials, methods, and acceptance criteria for tests and studies. - Establishing protocols for proper sample collection, labeling, storage, and processing to prevent contamination or mix-ups. - Effectively conveying complex scientific concepts clearly and concisely and engaging in group meetings and contributing to scientific discussions. - Regular upkeep and troubleshooting of laboratory equipment. - Providing comprehensive training to laboratory personnel to ensure competence and adherence to GLP requirements. - Maintaining organized and clean laboratory environments with controlled conditions to minimize errors and ensure consistency. - Adhering & Implementing safety protocols and ethical guidelines; ensuring compliance and policies to prevent data tampering, including version control and secure storage of records. Qualification Required: - Master's degree in Organic Chemistry with 3-4 years of industrial experience. - Most desirable to have experience in Pharmaceutical or Excipient industry.,

The ADL Research Associate role at our organization in Vadodara requires 1-3 years of experience and a qualification of BSc/MSc Chemistry. As an ADL Research Associate, you will be responsible for developing, validating, and implementing analytical methods to support pharmaceutical product development. Your expertise in analytical instrumentation and regulatory guidelines will ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Collaborating closely with R&D, Quality Assurance (QA), and Regulatory Affairs teams, you will contribute to formulation development, stability studies, and technology transfers. Your key responsibilities will include developing and validating analytical methods for various substances, conducting routine and non-routine analysis using analytical instruments like HPLC, GC, UV-Vis Spectroscopy, FTIR, Dissolution Apparatus, and LC-MS, and ensuring accurate and reproducible results compliant with regulatory standards. You will also be involved in stability studies as per ICH guidelines, providing analytical data for regulatory submissions, and supporting method transfer activities to Quality Control (QC) laboratories and contract research organizations (CROs). Maintaining accurate laboratory records, adhering to GMP, GLP, and ALCOA+ principles, and improving analytical techniques for enhanced lab efficiency and compliance are integral aspects of this role. Troubleshooting analytical challenges, investigating deviations, and implementing CAPA in a timely manner will be part of your routine tasks. Your dedication to continuous process improvement and adherence to regulatory requirements such as FDA, ICH, USP, EP, BP, and WHO will contribute to the success of our organization. This is a full-time position with a day shift schedule. The ideal candidate will have a Bachelor's degree and at least 1 year of experience in HPLC. If you are passionate about analytical method development, regulatory compliance, and process improvement, we welcome you to apply for this challenging and rewarding opportunity.,

The Quality Control Specialist in our pharmaceutical company located in Thanjavur plays a crucial role in ensuring that all products adhere to quality standards and regulatory requirements before being released to the market. You will be responsible for conducting a variety of testing and analysis procedures on raw materials, in-process materials, and finished products. Your collaboration with the production team to identify and resolve quality issues will contribute to the continuous improvement of our quality systems and processes. Your key responsibilities will include performing routine and non-routine testing using various analytical techniques like HPLC, GC, and UV/VIS spectroscopy. Additionally, you will conduct microbiological testing, stability testing, and environmental monitoring as necessary. Recording and analyzing test results to ensure compliance with specified standards and regulatory requirements, maintaining detailed records, preparing Certificates of Analysis (COAs), and identifying deviations from standard specifications are essential aspects of this role. You will work closely with the production, research and development, and quality assurance teams to implement corrective and preventive actions, review production batch records, and participate in the development and validation of new analytical methods. Your involvement in internal audits and inspections to ensure compliance with quality systems and regulatory standards, along with recommending continuous improvements to enhance product quality and efficiency, will be paramount. To qualify for this position, you should hold a Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences, or a related field, with an advanced degree being preferred. A minimum of 2-5 years of experience in quality control within the pharmaceutical industry is required. Proficiency in analytical techniques like HPLC, GC, FTIR, and spectrophotometry, familiarity with GMP, GDP, and regulatory requirements, and strong attention to detail are crucial technical skills. Moreover, possessing excellent problem-solving skills, the ability to work collaboratively in a team environment, and relevant certifications such as Certified Quality Auditor or Six Sigma will be advantageous. Staying current with industry trends, regulatory updates, and advancements in analytical techniques will also be expected in this role.,

As an ADL Officer/Executive at our Analytical Development Laboratory (ADL) located in Changodar, Ahmedabad, Gujarat, India, you will be an integral part of our team dedicated to developing, validating, and executing analytical methods to ensure the quality and compliance of our pharmaceutical products. Your key responsibilities will include developing, optimizing, and validating analytical methods for raw materials, intermediates, and finished products using techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy while adhering to ICH guidelines. You will also be responsible for conducting routine quality control tests on pharmaceutical products, analyzing raw materials, in-process samples, and finished products for various physical and chemical parameters. In addition, you will play a crucial role in maintaining accurate and detailed laboratory records, preparing and reviewing standard operating procedures (SOPs) and analytical method documents, and ensuring regulatory compliance with GMP and GLP regulations. You will also be involved in the calibration, maintenance, and troubleshooting of laboratory equipment and collaborate closely with formulation, R&D, and production teams to support product development and troubleshooting. To be successful in this role, you should possess a Bachelor's or Master's degree in Science (Chemistry, Biochemistry) or Pharmacy, proficiency in analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy, familiarity with regulatory guidelines (e.g., ICH, FDA, EMEA), strong attention to detail, excellent organizational skills, effective communication, and teamwork abilities. Both freshers and experienced candidates are encouraged to apply. Joining our team will offer you the opportunity to be part of a dynamic environment committed to excellence in the pharmaceutical industry. We provide opportunities for professional growth, continuous learning, and the chance to make a meaningful impact on healthcare. This is a full-time, permanent position with benefits including commuter assistance, life insurance, and provident fund. The work location is in person. If you have 2 years of experience in pharmaceuticals and 1 year of experience in analytical chemistry, we welcome your application to join our team and contribute to our mission of ensuring quality and compliance in pharmaceutical product development.,