Job Opportunity: Production Engineer (IVD RT-PCR Medical Devices) About the Role We are looking for an experienced Production Engineer to join our team in the In Vitro Diagnostics (IVD) sector. This role involves managing daily production activities for RT-PCR medical devices, ensuring compliance with ISO 13485 and GMP standards, and driving efficiency, quality, and continuous improvement within the production process. Key Responsibilities Execute and monitor daily production activities for IVD RT-PCR medical device manufacturing. Ensure adherence to ISO 13485 and GMP guidelines throughout the production process. Operate and maintain critical production equipment. Coordinate with planning and supply chain teams to ensure timely availability of raw materials. Maintain inventory control of production materials and consumables. Maintain proper documentation including BMRs, batch records, line clearance reports, and deviation logs. Perform in-process checks to ensure consistency and quality of products. Monitor environmental conditions and ensure compliance with cleanroom protocols. Support validation activities (IQ, OQ, PQ) for equipment and processes. Identify and troubleshoot process-related issues and implement corrective actions. Participate in root cause analysis (RCA) and CAPA implementation for process deviations. Collaborate with QA/QC teams for batch release, product testing, and compliance. Support training of new team members and operators on SOPs and best practices. Monitor and record equipment calibration and preventive maintenance schedules. Review and revise SOPs, WI, and other controlled documents periodically. Contribute to continuous improvement initiatives to enhance productivity and efficiency. Coordinate with regulatory and audit teams during internal/external inspections. Report daily progress, issues, and production metrics to superiors. Qualifications B.Tech/ B.E in Biomedical, Instrumentation, Electronics, or Mechanical Engineering. 3 to 4 years of production experience in IVD medical device manufacturing. Knowledge of ISO 13485 and GMP compliance requirements. Strong problem-solving and troubleshooting skills. Proficiency in MS Office and documentation handling. Why Join Us? Opportunity to work with advanced RT-PCR medical device technology in the IVD sector. Collaborative work environment with exposure to cross-functional teams (QA/QC, Regulatory, Supply Chain). Professional growth through continuous learning and improvement initiatives. Be part of a mission-driven team ensuring quality healthcare solutions. n If this role excites you, lets connect!
About the Role We are seeking an experienced QC professional to ensure the quality and reliability of our IVD medical devices. This role involves hands-on laboratory work, validation, testing, and supporting product development through stringent quality control measures. Key Responsibilities & Skills Perform hands-on testing and validation using RT PCR, Spectrophotometer, pH Meter, Automatic Extraction Systems, and Gel Electrophoresis. Ensure rigorous quality control processes across all products. Lead quality checks for Extraction Kits (Silica Column & Magnetic Beads) and RT PCR Kits (Infectious disease, Cancer markers). Support continuous improvement in QC methodologies and processes. Demonstrate strong leadership, people management, and presentation skills. Creation of Standard Operating Procedures (SOPs). Preparing the stability study documentation. Complaint Handling. Perform Calibration & validation. Qualifications MSc in Biotechnology, Microbiology, Immunology (PhD is an advantage). 710 years of Quality Control experience in an IVD medical device manufacturing environment. Proficiency in MS Office and laboratory data management.
Job Opportunity: Automation Engineer Liquid Handling Systems | Limited Travel Requirement About the Role Were looking for an Automation Engineer to join our team at G2M, where we design and support liquid handling automation systems for molecular biology applications. In this role, youll work closely with scientists and engineers to bring workflows to life, ensuring seamless implementation and ongoing support. Key Responsibilities Develop and optimize automation scripts for molecular biology workflows (mainly NGS library prep). Install, calibrate, and validate liquid handling systems at customer sites. Provide technical support, troubleshooting, and routine maintenance. Collaborate with R&D and product teams to improve software and systems. Document workflows and ensure compliance with industry standards (GLP, ISO). What Were Looking For Degree in Engineering, Biotechnology, Molecular Biology, or related field. 5+ years experience with automated liquid handling platforms. Strong scripting/programming skills for automation software. Hands-on knowledge of molecular biology workflows. Willingness to travel for installations and support. Nice to Have Experience in a customer-facing or field-based role. Familiarity with LIMS or robotics integration. Strong communication and problem-solving skills. Why Join Us? Be part of a collaborative team at the intersection of biology and automation. Work on impactful projects that accelerate scientific discovery. Opportunities for growth, training, and career advancement. Exposure to cutting-edge technologies in biotech. n If this role excites you, lets connect!
Job Opportunity: Product Manager IVD Solutions About the Role We are looking for a dynamic Product Manager to manage the product life cycle of our In Vitro Diagnostics (IVD) solutions portfolio, including RT-PCR Kits, POC devices, NGS clinical assays, and Extraction Kits. The role requires strategic planning, execution of go-to-market strategies, and close collaboration with customers, sales teams, and channels to accelerate growth. Key Responsibilities Manage the product life cycle from strategic planning to tactical activities for the IVD solutions portfolio. Develop and execute go-to-market strategies, ensuring brand positioning and customer segmentation. Partner with sales teams for customer profiling and to create acquisition/retention strategies. Build and sustain relationships with key opinion leaders in the industry. Design and implement creative marketing and promotional campaigns, including product brochures and digital content. Develop and implement pricing strategies and conduct margin analysis for profitability. Support field staff by shortening sales conversion cycles and creating platforms for knowledge sharing. Plan and execute marketing programs and customer engagement activities with cross-functional teams. Work with supply chain teams for rolling forecasts and inventory management. Support lead management initiatives and conduct market mapping for new opportunities. Collaborate with sales managers on roadmap validation and analysis. Deliver product training, develop content, and structure digital resources for the sales team. Qualifications Graduate/Post Graduate with BGCI certification. 3–5 years of experience in product management, preferably in the IVD/Healthcare domain. Strong knowledge of brand positioning, customer segmentation, and marketing strategy. Excellent communication, leadership, and analytical skills. Why Join Us? Opportunity to work with a diverse IVD product portfolio (RT-PCR, POC, NGS, Extraction Kits). Collaborative and innovative work environment with cross-functional exposure. Professional growth through strategic projects and leadership responsibilities. Be part of a team that contributes to global healthcare advancements
Key Responsibilities Lead and manage the development and optimization of lyophilization processes for diagnostic reagents, enzymes, and formulations. Design formulations and excipient systems to ensure stability, activity retention, and product shelf-life. Collaborate with assay development teams to ensure compatibility of lyophilized reagents with molecular diagnostic kits. Conduct scale-up studies and oversee production for mass manufacturing. Support regulatory documentation, stability studies, and validation protocols. Troubleshoot formulation challenges and drive continuous process improvement. Mentor junior scientists and provide technical leadership in formulation sciences. What Were Looking For • 5+ years of experience in lyophilization, formulation development, or related field. • PhD/Master’s in Pharmaceutical Sciences, Biotechnology, Biochemistry, or a related discipline. • Strong expertise in lyophilization cycle design, excipient selection, and formulation science. • Hands-on experience with diagnostic reagents, enzymes, or biologics. • Knowledge of analytical methods for stability and characterization. • Familiarity with cGMP, regulatory guidelines, and technology transfer. • Excellent problem-solving, project management, and teamwork skills. Nice to Have Experience in leading cross-functional R&D projects. Knowledge of advanced stabilization strategies for biologics. Strong communication and leadership skills. Why Join Us? Be part of a pioneering team working at the forefront of molecular diagnostics. Work on impactful projects that enable reliable and accessible healthcare solutions. Opportunities for professional growth, training, and leadership development. Exposure to cutting-edge technologies in biotech and molecular sciences
Job Opportunity: Product Manager IVD Solutions About the Role We are looking for a dynamic Product Manager to manage the product life cycle of our In Vitro Diagnostics (IVD) solutions portfolio, including RT-PCR Kits, POC devices, NGS clinical assays, and Extraction Kits. The role requires strategic planning, execution of go-to-market strategies, and close collaboration with customers, sales teams, and channels to accelerate growth. Key Responsibilities Manage the product life cycle from strategic planning to tactical activities for the IVD solutions portfolio. Develop and execute go-to-market strategies, ensuring brand positioning and customer segmentation. Partner with sales teams for customer profiling and to create acquisition/retention strategies. Build and sustain relationships with key opinion leaders in the industry. Design and implement creative marketing and promotional campaigns, including product brochures and digital content. Develop and implement pricing strategies and conduct margin analysis for profitability. Support field staff by shortening sales conversion cycles and creating platforms for knowledge sharing. Plan and execute marketing programs and customer engagement activities with cross-functional teams. Work with supply chain teams for rolling forecasts and inventory management. Support lead management initiatives and conduct market mapping for new opportunities. Collaborate with sales managers on roadmap validation and analysis. Deliver product training, develop content, and structure digital resources for the sales team. Qualifications Graduate/Post Graduate with BGCI certification. 3–5 years of experience in product management, preferably in the IVD/Healthcare domain. Strong knowledge of brand positioning, customer segmentation, and marketing strategy. Excellent communication, leadership, and analytical skills. Why Join Us? Opportunity to work with a diverse IVD product portfolio (RT-PCR, POC, NGS, Extraction Kits). Collaborative and innovative work environment with cross-functional exposure. Professional growth through strategic projects and leadership responsibilities. Be part of a team that contributes to global healthcare advancements
Job Opportunity: Production Engineer (IVD RT-PCR Medical Devices) About the Role We are looking for an experienced Production Engineer to join our team in the In Vitro Diagnostics (IVD) sector. This role involves managing daily production activities for RT-PCR medical devices, ensuring compliance with ISO 13485 and GMP standards, and driving efficiency, quality, and continuous improvement within the production process. Key Responsibilities Execute and monitor daily production activities for IVD RT-PCR medical device manufacturing. Ensure adherence to ISO 13485 and GMP guidelines throughout the production process. Operate and maintain critical production equipment. Coordinate with planning and supply chain teams to ensure timely availability of raw materials. Maintain inventory control of production materials and consumables. Maintain proper documentation including BMRs, batch records, line clearance reports, and deviation logs. Perform in-process checks to ensure consistency and quality of products. Monitor environmental conditions and ensure compliance with cleanroom protocols. Support validation activities (IQ, OQ, PQ) for equipment and processes. Identify and troubleshoot process-related issues and implement corrective actions. Participate in root cause analysis (RCA) and CAPA implementation for process deviations. Collaborate with QA/QC teams for batch release, product testing, and compliance. Support training of new team members and operators on SOPs and best practices. Monitor and record equipment calibration and preventive maintenance schedules. Review and revise SOPs, WI, and other controlled documents periodically. Contribute to continuous improvement initiatives to enhance productivity and efficiency. Coordinate with regulatory and audit teams during internal/external inspections. Report daily progress, issues, and production metrics to superiors. Qualifications B.Tech/ B.E in Biomedical, Instrumentation, Electronics, or Mechanical Engineering. 3 to 4 years of production experience in IVD medical device manufacturing. Knowledge of ISO 13485 and GMP compliance requirements. Strong problem-solving and troubleshooting skills. Proficiency in MS Office and documentation handling. Why Join Us? Opportunity to work with advanced RT-PCR medical device technology in the IVD sector. Collaborative work environment with exposure to cross-functional teams (QA/QC, Regulatory, Supply Chain). Professional growth through continuous learning and improvement initiatives. Be part of a mission-driven team ensuring quality healthcare solutions. n If this role excites you, lets connect!
Job Opportunity: Production Engineer (IVD RT-PCR Medical Devices) About the Role We are looking for an experienced Production Engineer to join our team in the In Vitro Diagnostics (IVD) sector. This role involves managing daily production activities for RT-PCR medical devices, ensuring compliance with ISO 13485 and GMP standards, and driving efficiency, quality, and continuous improvement within the production process. Key Responsibilities Execute and monitor daily production activities for IVD RT-PCR medical device manufacturing. Ensure adherence to ISO 13485 and GMP guidelines throughout the production process. Operate and maintain critical production equipment. Coordinate with planning and supply chain teams to ensure timely availability of raw materials. Maintain inventory control of production materials and consumables. Maintain proper documentation including BMRs, batch records, line clearance reports, and deviation logs. Perform in-process checks to ensure consistency and quality of products. Monitor environmental conditions and ensure compliance with cleanroom protocols. Support validation activities (IQ, OQ, PQ) for equipment and processes. Identify and troubleshoot process-related issues and implement corrective actions. Participate in root cause analysis (RCA) and CAPA implementation for process deviations. Collaborate with QA/QC teams for batch release, product testing, and compliance. Support training of new team members and operators on SOPs and best practices. Monitor and record equipment calibration and preventive maintenance schedules. Review and revise SOPs, WI, and other controlled documents periodically. Contribute to continuous improvement initiatives to enhance productivity and efficiency. Coordinate with regulatory and audit teams during internal/external inspections. Report daily progress, issues, and production metrics to superiors. Qualifications B.Tech/ B.E in Biomedical, Instrumentation, Electronics, or Mechanical Engineering. 3 to 4 years of production experience in IVD medical device manufacturing. Knowledge of ISO 13485 and GMP compliance requirements. Strong problem-solving and troubleshooting skills. Proficiency in MS Office and documentation handling. Why Join Us? Opportunity to work with advanced RT-PCR medical device technology in the IVD sector. Collaborative work environment with exposure to cross-functional teams (QA/QC, Regulatory, Supply Chain). Professional growth through continuous learning and improvement initiatives. Be part of a mission-driven team ensuring quality healthcare solutions. n If this role excites you, lets connect!
Role & responsibilities We are looking for a highly skilled QA professional with expertise in IVD medical devices. The role requires strong knowledge of international regulatory compliance, audits, product registration, and documentation, ensuring that our products meet the highest standards of quality and safety Preferred candidate profile Lead and manage audits (ISO:13485, CDSCO) and IVDR transitions. Handle product registrations across multiple geographies (FDA, CE-IVDR, Thailand, Vietnam, Malaysia, Saudi Arabia). Prepare and compile technical documentation such as DMF, GSPR, Risk Assessments, SOPs, and Labeling requirements. Ensure compliance with regulatory standards in all product and process areas. Demonstrate strong leadership, people management, and presentation skills. Work with products such as Extraction Kits (Silica Column & Magnetic Beads) and RT PCR Kits (Infectious disease, Cancer markers). Qualifications MSc in Biotechnology, Microbiology, Immunology (PhD is an advantage). 710 years of Quality Assurance experience in an IVD medical device manufacturing environment. Proficiency in MS Office and documentation management.