Executive Jobs: Molbio Diagnostics is Hiring for an Executive Position | Apply Now for Biotech Career | Life Science Jobs
Searching for life science jobs to
advance your Biotech Career? Molbio Diagnostics is hiring an Executive / Sr. Executive – Technology Transfer in Goa, India. This Executive job role is ideal for professionals passionate about bridging R&D innovations with large-scale manufacturing. The position focuses on design implementation, process validation, and seamless technology transfer to ensure quality, compliance, and production excellence for Molbio’s advanced PCR products and diagnostic devices.Job Details:
- Position: Executive / Sr. Executive – Technology Transfer
- Location: Goa, India
- Job Type: Full-time | On-site
About the Company:
Molbio Diagnostics is a leading Indian healthcare technology company revolutionizing molecular diagnostics through its innovative Truenat platform—a portable, battery-operated real-time PCR system that brings lab-accurate results to the point of care. Headquartered in Goa, Molbio focuses on accessible, rapid, and reliable diagnostic solutions for infectious and non-infectious diseases, empowering healthcare systems across urban and rural settings.
The company’s commitment to research, innovation, and public health impact has positioned it as a global leader in point-of-care molecular diagnostics. With strong collaborations in healthcare and continuous investment in technology, Molbio Diagnostics continues to bridge the gap between advanced science and real-world clinical needs—making high-quality diagnostics available to all.
Education:
Ph.D. in Life Sciences, Microbiology, Biotechnology or related areas.
Key Responsibilities:
- Collaborate with R&D to understand product technology and support new product introductions in manufacturing.
- Review design transfer files and ensure complete validation and compliance.
- Identify and mitigate risks associated with design and implementation, including technical and regulatory challenges.
- Plan and execute product and process validation activities, including design file reviews and protocol development.
- Validate methods, equipment, software, raw materials, and facilities as per defined standards.
- Troubleshoot production and quality issues to maintain process efficiency.
- Develop effective manufacturing strategies with the executive team to ensure scalability and performance.
- Stay updated on emerging manufacturing technologies and apply them to improve productivity and product quality.
- Analyze manufacturing data to drive process improvements and ensure machine maintenance.
- Maintain full compliance with national and international regulatory standards.
Experience:
- 2–5 years post-Ph.D. or 6–8 years post-Master’s experience in the medical device or POC IVD industry.
- Strong understanding of CDSCO, ISO 13485, IVDR, and MDSAP regulations.
- Proven experience with RTPCR R&D processes and Design Transfer activities.
Skills & Competencies:
- In-depth knowledge of QMS, QC, QA, GMP, GLP, ISO, and FDA standards.
- Hands-on experience in scale-up feasibility studies for new product manufacturing.
- Proficiency in product design documentation, verification, and validation.
- Experience in process development, automation, and statistical process control.
- Trained in Lean Six Sigma, production management, and data interpretation.
- Strong analytical and problem-solving skills with strategic thinking and attention to detail.
- Excellent communication and project execution abilities.
