Role & responsibilities Promotion of Product coming under TM Division (Blood Collection Bags, Filter Bags, ACD Bags, Blood bank Equipment, ACE machine etc.) to blood bank, Institutional buyers and other Agencies, Developing and serving network of channel partners to effectively meet the needs of the customers, Work with team & demonstrate by leading and front, Achieving the monthly, Quarterly and yearly revenue/customer creation / patient engagement months targets, Effectively following with the institutional customers,implementing the strategies and policies of the division, Developing good customer connect with blood bank professionals and Technicians. Identifying business opportunities in private and institutional markets, sharing of the information proactively to the seniors, Preparation of weekly,monthly reports,secondary billing details from channel partners,competitors activities, Implementing the brand building, promotional activities by coordinating with Regional / HO team, Preparation and updating database of customers for business analytics, Conduct workhop/CME,

Role & responsibilities Design, Develop, and maintain application for internal and external user using VB.Net. PHP, ad C#, Work with Microsoft SQL Server and Microsoft Access databases to generate and retrieve information for software development, Should be Experience on Window Application, Ensure application performance, Security and scalability, API generation and security for smooth running of application, Debug and resolve software defects and issues, Collaborate with external stakeholders and vendors for outsourced projects, Proficiency in VB.Net, PHP, and C# Programming Languages, Solid understanding of MS SQL AND MICROSOFT development best Practices, Including version control, testing and deployments, Familiarity with LDAP integration for authentication and security,

Role & responsibilities Supervision and monitoring of work in BB line particularly for Mixing, Filling and pouching as per respective SOP and maintaining discipline in work area. In process monitoring to check quality of product at each stage of process and provide on job training to concern workers. Maintaining and hygiene condition in clean room as per respective SOP. On line documentation as per requirement. Ensure timely availability of material for smooth production. Weighing and checking of raw material as per requirement. Ensuring Smooth material Flow for timely availability of material of semi finish good machine and equipment at each stage of process. Maintaining identification status of process, material, semi finish good, machine and equipment at each stage of process. Monitoring of rejection at various stage of process and analyze it and reduce it by effective monitoring, analyzing and eliminating the root cause. Ensuring timely and efficient execution of production targets. To take prompt action for any break down maintenance as well as preventive maintenance of machines and equipment. Maintaining inner department coordination as per requirement.

Role & responsibilities Preparation of invoice of CAPD, Blood bag and Accessories Responsible for physical checking of according to invoice. Pre-Dispatch lntimation to QA To maintain temperature and cleaning record on daily basis. Responsible for loading of finished goods properly Other billing (Stent & Scrap etc.) as per requirement Filling of documents properly such as invoice Handle Export billing and related documents Manage logistic independently and coordinate with other team accordingly

Role & responsibilities Handling of breakdown related to Electronic faults. Experience on Servo Motor Handling and maintenance of Automation works. Handling and maintenance of SCADA operated panels. Handling of PLC and its programming. Handling of AC/DC drivers. Preventive maintenance of production / Utility machines. In absence, change shall be handed over to design. Any other task assigned by the reporting Manager/ Seniors. Functional reporting shall be as per departmental organogram.

Role & responsibilities Preparation, Review and updation of Technical Files as per euMDR 2017/745 & DMF as per IMDR. General performance and safety records as per respective Guidelines. Risk Management plan & reports as per respective guidelines. Clinical Evaluation protocol & Report as per respective Guidelines. PMS,PMCF & PSUR plan & report as per respective Guidelines. Design & Development documentation & report as per respective Guidelines. Usability engineering protocol & report as per respective Guidelines. Track & Trend & report all Re-portable events,including serious/ adverse incidence, field safety corrective Keep up to date with national and international legislation,guidelines and customer practice. In absence, charge shall be handed over to the designee.

Role & responsibilities Prepare and maintain accurate financial statements and reports in a timely manner. Manage the budgeting, forecasting, and long-term financial planning processes. Ensure full compliance with applicable tax regulations, including GST, TDS, and income tax filings. Conduct internal and statutory audits, ensuring compliance with auditing standards. Supervise accounts payable and receivable functions to ensure efficient cash flow management Assist in identifying financial risks and implementing cost control measures Monitor and ensure compliance with applicable accounting standards Work on both direct and indirect taxes, ensuring timely and accurate filings. Utilize SAP software for accounting, reporting, and process automation. Analyze financial performance and provide data-driven insights to senior management for decision-making. Maintain and oversee accounting systems and processes, ensuring accuracy and integrity of financial data Liaise with external auditors, tax consultants, and regulatory authorities as required

We are looking for a skilled and detail-oriented QA Executive to join our team. The candidate will be responsible for ensuring the quality and regulatory compliance of medical devices in line with EU MDR 2017/745 and Indian Medical Device Rules (IMDR). This role involves preparing, reviewing, and updating key technical and regulatory documentation and supporting post-market surveillance activities. Roles & Responsibilities Preparation, review, and updating of Technical Files as per EU MDR 2017/745 and Device Master Files (DMF) as per IMDR . Maintenance of General Safety and Performance Requirements (GSPR) documentation in compliance with applicable guidelines. Preparation of Risk Management Plans and Reports as per ISO 14971 and other applicable standards. Development and review of Clinical Evaluation Protocols and Reports (CEP/CER) as per MDR/IMDR guidelines. Preparation and maintenance of Post-Market Surveillance (PMS) , Post-Market Clinical Follow-up (PMCF) , and Periodic Safety Update Reports (PSUR) . Documentation of Design and Development activities, ensuring alignment with regulatory and internal design control requirements. Drafting and reviewing Usability Engineering Protocols and Reports in compliance with ISO 62366. Monitoring, tracking, trending, and reporting of all reportable events , including serious/adverse incidents and field safety corrective actions (FSCA) . Keeping up to date with current national and international regulations, standards, and best practices relevant to the medical device industry. Ensure proper handover of responsibilities to designated personnel during absence. Desired Candidate Profile Prior experience in quality assurance or regulatory affairs for medical devices. In-depth understanding of EU MDR 2017/745 , IMDR , and related standards (e.g., ISO 13485, ISO 14971, ISO 62366). Strong documentation and review skills. Attention to detail with good organizational and analytical abilities. Effective communication skills and the ability to work independently as well as in a cross-functional team.