About Alkem MedTech Pvt Ltd:Alkem MedTech Pvt Ltd is a wholly owned subsidiary of Alkem Laboratories Ltd, which is the 5th largest listed Pharmaceutical company in terms of market share. As the first MedTech venture of Alkem Labs, Alkem MedTech is dedicated to advancing precision, high-risk, and implantable medical devices along with their accessories. MedTech is a strategic priority for Alkem Labs, representing a significant growth avenue. We are beginning our MedTech journey by focusing on Musculoskeletal solutions and have plans to expand into multiple segments, establishing a robust, multi-faceted MedTech company in the near future.Alkem MedTech will be manufacturing in India, aligning with the vision of the Government of India to boost domestic production and innovation in the medical technology sector.We are looking for passionate and innovative talents to join our pioneering team. If you are excited about shaping the future of medical technology and want to be part of a transformative journey, Alkem MedTech is the place for you.Why Join Us?Innovation-Driven Environment: Work on cutting-edge technologies in precision and implantable medical devices.Growth Opportunities: Be part of a strategic growth initiative for one of the leading pharmaceutical companies and be part of creating a legacy.Collaborative Culture: Engage with a team of dedicated professionals committed to making a difference in healthcare.Impactful Work: Contribute to life-changing medical solutions in the Musculoskeletal segment and beyond.Manufacturing in India: Support the vision of the Government of India by contributing to domestic production and innovation in the MedTech sector.Join us at Alkem MedTech and help shape the future of healthcare technology.Purpose of the role: The Design Quality Engineer will be responsible for ensuring the design, development, and manufacturing processes comply with regulatory requirements, industry standards, and company quality policies. This role will involve close collaboration with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, and Quality Assurance. Roles & Responsibilities:Ensure design control activities comply with applicable regulations (e.g., FDA 21 CFR Part 820, ISO 13485) and standards (e.g., ISO 14971, IEC 62366).Participate in design reviews and provide quality engineering support throughout the product development lifecycle.Establish and maintain Design History Files (DHF) and Risk Management Files (RMF).Conduct design verification and validation activities, ensuring product safety and efficacy.Develop and implement risk management activities including Failure Mode and Effects Analysis (FMEA).Collaborate with cross-functional teams to ensure effective design transfer from R&D to manufacturing.Support the creation and review of technical documentation, including design inputs/outputs, specifications, and reports.Manage non-conformances, CAPAs, and change management activities related to design quality.Provide guidance on regulatory requirements and standards related to orthopedic implant design.Participate in internal and external audits, including regulatory inspections.

Alkem MedTech Pvt Ltd is a wholly owned subsidiary of Alkem Laboratories Ltd, which is the 5th largest listed Pharmaceutical company in terms of market share. As the first MedTech venture of Alkem Labs, Alkem MedTech is dedicated to advancing precision, high-risk, and implantable medical devices along with their accessories. MedTech is a strategic priority for Alkem Labs, representing a significant growth avenue. We are beginning our MedTech journey by focusing on Musculoskeletal solutions and have plans to expand into multiple segments, establishing a robust, multi-faceted MedTech company in the near future.Alkem MedTech will be manufacturing in India, aligning with the vision of the Government of India to boost domestic production and innovation in the medical technology sector.We are looking for passionate and innovative talents to join our pioneering team. If you are excited about shaping the future of medical technology and want to be part of a transformative journey, Alkem MedTech is the place for you. Why Join Us?Innovation-Driven Environment: Work on cutting-edge technologies in precision and implantable medical devices.Growth Opportunities: Be part of a strategic growth initiative for one of the leading pharmaceutical companies and be part of creating a legacy.Collaborative Culture: Engage with a team of dedicated professionals committed to making a difference in healthcare.Impactful Work: Contribute to life-changing medical solutions in the Musculoskeletal segment and beyond.Manufacturing in India: Support the vision of the Government of India by contributing to domestic production and innovation in the MedTech sector.Join us at Alkem MedTech and help shape the future of healthcare technology.Purpose of the role: The Microbiologist is responsible for ensuring the sterility of orthopedic knee and hip joint implants, monitoring microbiological processes, conducting microbiological testing, and ensuring compliance with relevant standards and regulations. This role involves conducting environmental monitoring, sterilization validation, and contamination control to ensure product safety and quality. Perform microbiological testing of raw materials, in-process samples, finished products, and environmental samples in accordance with GMP (Good Manufacturing Practices) and ISO standards.Conduct sterility testing, endotoxin testing, and bioburden testing of implants and related materials.Monitor and maintain environmental controls in cleanrooms, including air, surface, and personnel monitoring.Validate sterilization processes (e.g., Ethylene Oxide, Gamma Radiation) and perform routine sterilization cycle monitoring.Investigate microbial contamination events and implement corrective and preventive actions (CAPA).Maintain microbiological laboratory instruments, ensuring calibration, validation, and proper maintenance.Prepare detailed reports on microbiological findings, test results, and environmental monitoring data.Ensure compliance with regulatory requirements including FDA, ISO 13485, and EU MDR.Provide microbiological support during audits and inspections by regulatory bodies.Develop and review microbiological standard operating procedures (SOPs) and test protocols.Train and mentor junior staff on microbiological procedures and aseptic techniques.