Senior Scientist- Chemistry

3 weeks ago


Pune HO, India Module Innovations Full time
About Module Innovations

We are a pioneering company in the field of diagnostic solutions for infectious diseases and antimicrobial resistance. Our mission is to preserve the lifesaving efficacy of antibiotics by providing rapid diagnostic results. We are seeking a highly skilled Senior Scientist- Chemistry to join our multidisciplinary team.

Job Purpose

The successful candidate will be responsible for the hands-on development of biosensors, assay development, and troubleshooting. They will design, plan, and conduct experiments using different immunoassays and devise novel technologies. The ideal candidate will have expertise in materials and conjugation chemistry characterization methods and data interpretation.

Key Responsibilities
  • Design, plan, and conduct experiments using different immunoassays and devise novel technologies.
  • Perform nanomaterial synthesis, surface modification, and bioconjugation.
  • Expertise in materials and conjugation chemistry characterization methods and data interpretation.
  • Design, conduct, and oversee product development experiments/studies and maintain records in accordance with QMS.
  • Develop and implement novel methodologies and technologies to advance Module's product development research.
  • Evaluate their feasibility, demonstration, and potential risks.
  • Procure chemicals and raw materials for research and development.
  • Execute project plans and conduct research within timelines for existing product efficiency/quality improvisation.
  • Perform statistical analysis and record it throughout the design and development of a product to ensure the validity and reliability of the study findings.
  • Develop testing methodology and execute as required for the evaluation of new/existing products. Analyze and interpret test results, making necessary design revisions based on findings.
  • Evaluate stability testing of test reagents according to CLSI EP25.
  • Design, plan, and conduct clinical validation of the product/s and its analysis. Engage with clinicians, clinical microbiologists, lab technicians, and maintain documentation for the same.
  • Identify and implement improvements to existing procedures, methods, and techniques to enhance efficiency and productivity.
  • Prepare manuscripts for research publications. Ensure research is published in high-impact journals.
  • Evaluate patentability of new technologies in the area of work.
  • Prepare project reports, technical presentations, and SOPs.
  • Train and supervise junior team members, work closely with them, and ensure that milestones are met within timelines.
  • Support the organization by preparing and maintaining documents for audits for the Quality Management System (QMS).
  • Prepare reports and documents for regulatory compliance, including CDSCO, 510(k) submissions, or CE Mark applications, and support regulatory reviews.
  • Present project updates, findings, and recommendations to management and regulatory bodies.
  • Maintain detailed records of all development activities, including design changes and test results.
  • Follow and ensure aspects related to safety, ethics, confidentiality, and legal compliance.
  • Stay updated with the latest advancements and trends in the field of biosensors. Recommend and implement new methodologies as appropriate.
  • Perform in-charge duties for the allocated lab/equipment/inventory/supporting activities and take responsibility for the timely completion of tasks assigned.
  • Ensure full compliance with safety, health, and environmental (EHS) guidelines according to Module's standards in all areas of responsibility. Promote safety behavior according to the above guideline.
  • Actively participate in the planning and execution of Module's extracurricular activities, such as workshops, AMR seminars, etc.
Preferred Skills
  • Knowledge in nanomaterial synthesis, surface modifications, bioconjugation methods.
  • Hands-on experience in performing immunoassays like ELISA, dot blots, lateral-flow assay, and handling instruments like UV-Vis spectrophotometer, Centrifuge, Weighing balance, vacuum manifold, etc.
  • Strong data analysis skills and proficiency with relevant software (e.g., statistical tools, bioinformatics platforms).
  • Expertise in manuscript/patent writing, poster, and IFU making.
  • Ability to handle multiple tasks simultaneously, set priorities, and work independently and flexibly with a strong commitment to excellence.
  • Must be a self-starter, able to work independently, willing to take initiative, and demonstrate efficient and effective time management.
  • Excellent written and oral communication skills and a proven ability to work well on a multidisciplinary team of scientists and engineers.
  • Excellent problem-solving abilities and attention to detail.
  • Leadership and team management capabilities.
  • Ability to work in a fast-paced startup environment.
  • Knowledge in CLSI EP25 guidelines.
  • Strong grasp and significant experience working with Microsoft Excel, PowerPoint, and Word.
  • Excellent communication (written and verbal) and documentation skills in English.
  • Experience working with software like 2D NMR processor, ImageJ, as well as other software such as Origin, MATLAB, Python, Adobe Illustrator, Blender, and GraphPad Prism is an advantage.
  • Knowledge of and experience with quality management systems, such as GMP, HACCP, and ISO 13485.


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