Senior Scientist- Chemistry

1 month ago

Pune, India Module Innovations Full time

About Module:

We are building Innovative diagnostic solutions for Infectious disease and Anti-Microbial Resistance (AMR). Module is leveraging the power of Nanotechnology and Biotechnology to create powerful solutions for ultra rapid diagnosis of Urinary Tract Infection (UTI) and Anti-microbial Susceptibility of the uropathogen. Antibiotics are lifesaving drugs, but rapidly emerging antimicrobial resistance is threatening that reality. Module Innovations’s mission is to preserve the lifesaving efficacy of antibiotics by providing diagnostic results in hours, rather than days, and we are building a multidisciplinary team of talented individuals to help achieve this mission.

Joining the Module team will give you an opportunity to harness your talent and advance your career by working with diverse and high-performing teammates tackling the most important healthcare challenges.

More at www.moduleinnovations.com


Job Opening: Senior Scientist- Chemistry

Required Qualifications


Education:

PhD / Post-doctoral in Chemistry or Bioengineering / Biomedical engineering / Chemical Engineering / Materials Science / Physical chemistry / Biotechnology / Biochemistry, or related fields


Experience:

o  PhD with 3+ years or post-doc with 1+ years of experience in chemistry or other field with applications in biomedical / life science area

o  Experience working in a national/international research institute or in a regulated industry, such as pharmaceuticals, in-vitro medical device development

o  Certification in relevant professional organisations, such as the American Chemical Society (ACS), is an asset

o  Demonstrated success in leading research projects and publishing scientific papers/patents.


Job Purpose:

  • Hands-on development of biosensors, assay development and its troubleshooting and translate the protocol to other team members.
  • Design, plan and conduct experiments using different immunoassays and devise novel technologies.
  • Perform nanomaterial synthesis, surface modification and its bioconjugation
  • Expertise in materials and conjugation chemistry characterization methods and its data interpretation
  • Design, conduct, and oversee product development experiments/studies and maintain its 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.
  • Procurement of 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. Analyse and interpret test results, making necessary design revisions based on findings
  • Evaluation of 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.

  • Preparation of project reports, technical presentations and SOP’s
  • Train and supervise the junior team, work closely with them, and make sure that the milestones are met within timelines.
  • Support the organization by preparing and maintaining the 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.
  • Follows and ensures 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
  • Performs in-charge duties for the allocated lab/equipment/inventory/supporting activities and takes responsibility for the timely completion of the tasks assigned
  • Performs other duties as assigned
  • Ensure full compliance with safety, health, and environmental (EHS) guidelines according to Module’s standards in all areas of responsibility. Promote safety behaviour according to the above guideline

·     Actively participate in the planning and execution of the 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


Preferred Knowledge

·     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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