Careers

Openings at Module Innovations

  1. Product Manager
  2. Senior Scientist- Chemistry
  3. Senior Scientist- Microbiology

Interested candidates may apply using the link given below by 10th October 2024 

Click here to Apply :

Read the Job Description below

 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

Details of the job

 

Job Title No. of post/s
Product manager 1
Senior Scientist-Chemistry 1
Senior Scientist-Microbiology 1
Application deadline 10-10-2024
Application Mode Online, Google form submission
Google form link https://forms.gle/YDwEWhXqEb17eRe26

 

Job Summary:

Are you a highly motivated and independent professional with a passion for innovation? We’re seeking a Product Manager and Senior Scientists to join our dynamic team at Module. The mission of Product Manager is to strategize the full lifecycle of a product, from conception to release by ensuring compliance with quality standards and regulatory requirements. The mission of Senior Scientists is to drive the development, improvement, and verification of Module products while ensuring compliance with quality standards and regulatory requirements. These roles also involve applying technical knowledge to create accurate, reliable, and innovative diagnostic tests, while collaborating with cross-functional teams to bring these diagnostic solutions to market. It is typically based in a laboratory setting with occasional fieldwork or travel as required.

Job Title 1 Product Manager

 

Required Qualifications

  • Education:
  • Tech / MS /M.Sc. / PhD in Bioengineering / Biomedical engineering / Chemical Engineering / Materials Science / Physical chemistry / Biotechnology / Biochemistry, Life Science or related fields
  • Experience:
  • Tech/MS/M.Sc. with 5+ years in biomedical / life science applications or PhD with 1+ years of experience is an asset
  • Experience working in a national/international research institute or in a regulated industry, such as pharmaceuticals, in-vitro medical device development
  • Certificate for an internal auditor for ISO 13485:2016 is an asset
  • Proven track record of successfully launching and managing in-vitro medical device in accordance with CDSCO regulations

Job Purpose:

  • Conduct market research and competitive analysis to identify opportunities and threats.
  • Develop comprehensive project plans, including timelines, milestones and resource allocation
  • Define project scope, objectives, and deliverables in collaboration with senior management and stakeholders.
  • Identify and mitigate project risks and issues, ensuring timely resolution and escalation when necessary.
  • Facilitate effective communication and collaboration among team members, stakeholders, and external partners
  • Ensure products meet quality standards and regulatory requirements
  • Stay updated on industry trends and emerging technologies to drive innovation
  • Work closely with teams to develop go-to-market strategies and launch plans
  • Track and report on product development metrics, including timelines, budgets, and performance outcomes.
  • Provide regular updates to senior management on project status and key milestones
  • Evaluation and documentation for Design and Development of in-vitro medical device and maintain its records in accordance with QMS.
  • Conduct regular project reviews and audits to ensure compliance and identify areas for improvement
  • Evaluate clinical validation of the product and ensure the quality is met. Engage with R&D team, clinicians, clinical microbiologists, lab technicians and maintain documentation for the same
  • Facilitate project meetings, presentations, and reports for stakeholders at various levels
  • 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.
  • Follows and ensures aspects related to safety, ethics, confidentiality, and legal compliance
  • 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 according to the above guideline
  • Actively participate in the planning and execution of the Module’s extracurricular activities such as workshops, AMR seminars, tech showcase etc

Preferred skills:

  • 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 of CDSCO MDR 2017 guidelines
  • Knowledge of Project management software/tools like JIRA, Zoho
  • Strong grasp and significant experience working with Microsoft Excel, PowerPoint, Word and other product management tools
Job Title 2 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:
    • PhD with 3+ years or post-doc with 1+ years of experience in chemistry or other field with applications in biomedical / life science area
    • Experience working in a national/international research institute or in a regulated industry, such as pharmaceuticals, in-vitro medical device development
    • Certification in relevant professional organizations, such as the American Chemical Society (ACS), is an asset
    • 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

 

Job Title 3 Senior Scientist-Microbiology

 

Required Qualifications

  • Education:
  • D. in Microbiology, Molecular Biology, Immunology, or a related field
  • Experience:
    • PhD with 3+ years and post-doc with 1+ years of experience
    • Experience working in a national/international research institute or in a regulated industry, such as pharmaceuticals, in-vitro medical device company
    • Certification in relevant professional organizations, such as the American Society for Microbiology (ASM), is an asset
    • Demonstrated success in leading research projects and publishing scientific papers/patents.

Job Purpose

  • Conduct antimicrobial susceptibility testing (AST) and MIC determination using Module’s proprietary technology and validate the accuracy with gold standard methods in accordance with CLSI guidelines
  • Procurement of bacterial strains from ATCC, IHMA, NCIM or other organizations. Coordinate with partner hospitals.
  • Maintenance of culture stock at Module’s repository.
  • Design, conduct, and oversee other microbiological experiments and 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.
  • 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 for 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 microbiological procedures, methods, and techniques to enhance efficiency and productivity.
  • Review literature and competition, while devising ways to further enhance Module’s product performance.
  • Prepare manuscripts for research publications
  • 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 AST and 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

  • Expertise in microbiological techniques, including culturing, antimicrobial susceptibility testing (AST), MIC, genetic profiling, sequencing etc.
  • Expertise in performing experiments with pathogenic/clinical isolates in BSL-2 facility
  • Proficient in using AST testing equipment like VITEK and software
  • The candidate must have a thorough knowledge of CLSI guidelines for antimicrobial susceptibility testing (AST) such as M100, M07
  • Candidate must have hands-on experience in performing immunoassays like ELISA, dot blots, and handling instruments like Crocodile 5 in 1 ELISA plate reader, UV-Vis. spectrophotometer, Microplate reader, Densitometer, Centrifuge, Weighing balance, SDS page, vacuum manifold, and autoclave
  • 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.
  • 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 (M100, M07, 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 such as Origin, MATLAB, Adobe Illustrator, Blender and GraphPad Prism is an advantage
  • Knowledge of and experience with quality management systems, such as GMP, HACCP, and ISO 13485