4 Analytical Software Jobs

As the Deputy General Manager at the Peadiatric Cancer Research Institute (PCRI) in HQ, Delhi, you will play a crucial role in the implementation and initiation of research studies. This includes writing research proposals, developing study protocols and tools, training research staff, ensuring data collection and analysis efficiency, and monitoring staff to maintain quality assurance. Your responsibilities will also involve enhancing data use for improving service quality and decision-making within the organization. Your key tasks will include overseeing the development of a robust Monitoring & Evaluation (M&E) framework and Management Information System (MIS) using various tools. You will be responsible for analyzing data to provide evidence-based insights that drive efficient programming and results for the project. Additionally, you will be expected to disseminate research findings and project outcomes through presentations and publications. In your capacity, you will manage the PCRI department by preparing and overseeing budgets, recruiting and retaining high-quality staff, and engaging with advisory committees, decision-makers, and board members to align research goals with the organization's objectives. You will also collaborate with other departments within the organization to ensure seamless interdepartmental coordination. Your role will involve planning and executing research projects, providing technical expertise in research study development and analysis, and submitting grant proposals to secure funding. You will be instrumental in creating tools, processes, and systems to drive improvements and streamline departmental projects, such as setting up an ethics committee and maintaining project dashboards for effective monitoring and reporting. Furthermore, you will be responsible for managing and executing specific research projects like Access India, CVC study, RT mapping study, and CHSU evaluation to collect data that supports evidence-based planning and contributes to achieving global outcomes in terms of survival rates. Your duties will also encompass supporting Pan India activities, participating in national/international meetings and conferences, and coordinating with other departments for abstract submissions and presentations. In addition to the outlined responsibilities, you will be expected to perform any other job-related tasks assigned by your immediate supervisor. Your role as Deputy General Manager at PCRI will require a combination of program management skills, research methodology expertise, proficiency in analytical software tools, and a commitment to driving efficient project management practices that contribute to the organization's overarching goals.,

You will be joining our ARD team in Udaipur as an ARD Chemist / Scientist. Your main responsibilities will include method development and validation, impurity profiling, and instrumental analysis to assist our Synthesis R&D and quality operations. Your key responsibilities will include developing HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, validating HPLC methods suitable for AMV, performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, ensuring all analytical instruments are well-maintained, performing regular calibration and documentation of analytical instruments, maintaining proper records as per regulatory and internal quality standards, and supporting the preparation of SOPs, protocols, and technical reports. To excel in this role, you should possess a strong knowledge of HPLC, GC, and LC-MS techniques, have experience in method development and impurity profiling, be familiar with ICH guidelines and regulatory requirements, be proficient in analytical software like Empower/Chromeleon, and have good documentation and communication skills.,

As an ARD Chemist / Scientist at our Udaipur location, you will be a key member of our ARD team, responsible for method development and validation, impurity profiling, and instrumental analysis to support our Synthesis R&D and quality operations. Your primary responsibilities will include developing and validating HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, as well as developing HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC. You will also be tasked with performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, and ensuring that all analytical instruments are maintained in optimal working condition through regular calibration and documentation. In addition, you will play a crucial role in maintaining proper records as per regulatory and internal quality standards, supporting the preparation of SOPs, protocols, and technical reports, and ensuring compliance with ICH guidelines and regulatory requirements. To excel in this role, you must possess a strong knowledge of HPLC, GC, and LC-MS techniques, along with experience in method development and impurity profiling. Familiarity with analytical software such as Empower/Chromeleon, good documentation, and communication skills are also essential for success in this position.,

As a Polymorph Screening Scientist at Morepen Proprietary Drug Research Pvt Ltd. (MPDRPL), your primary responsibility will be to lead the screening and selection of solid forms for drug candidates. You will play a crucial role in improving the physicochemical properties of active pharmaceutical ingredients (APIs) by overseeing polymorph screening activities. It is essential to identify the most stable and bioavailable forms of drug substances for regulatory submissions. Collaborating with cross-functional teams, you will mentor junior scientists and drive advancements in solid-state drug discovery. Your key responsibilities will include overseeing the screening of potential polymorphs, solvates, and hydrates for APIs, interpreting and analyzing solid-state data, scaling up identified novel polymorphs, collaborating with various teams to align polymorph selection with drug formulation strategies, preparing regulatory-compliant data for filings, troubleshooting any issues related to polymorph stability, and ensuring accurate documentation and reporting of experimental protocols and findings. The deliverables expected from you include the identification and characterization of stable polymorphs and crystal forms for drug candidates, detailed screening reports, regulatory-compliant data for solid-state forms, and methodologies for high-throughput screening, scaleup, and solid-state characterization. To qualify for this role, you should hold a Ph.D. in Pharmaceutical Sciences, Solid state Chemistry, Chemistry, or a related field, with a focus on solid-state chemistry or materials science. Alternatively, a Master's degree with equivalent experience will be considered. You should have a minimum of 6+ years of industry experience in solid-state chemistry, polymorph screening, or pharmaceutical development and proven expertise in solid-state characterization techniques and polymorph screening methods. Proficiency in solid-state characterization methods, high-throughput screening techniques, and knowledge of computational techniques for polymorph prediction are essential technical skills required for this role. In addition to technical skills, you should possess excellent problem-solving, troubleshooting, and decision-making skills. Effective communication skills, both written and verbal, are crucial for presenting complex data to diverse audiences. Being detail-oriented with strong organizational and documentation skills will contribute to your success in this role at MPDRPL.,