Lead HR strategy and execution across corporate and plant levels, including organization design, workforce planning, and change management. Strong command over labor laws, HR compliance, and people processes in regulated environments (Factories Act, ESI, PF, CDSCO, ISO13485). End-to-end talent acquisition across R&D, manufacturing, quality, and commercial functions, along with employer branding and EVP initiatives. Manage complete plant HR operations including staffing, time-office, welfare, employee engagement, safety, and union relations if applicable. Design and manage compensation structures, incentive plans, payroll, and recognition programs benchmarked to industry standards. 12-18 years of progressive HR experience, preferably in medical devices, healthcare, pharma, or life sciences, with at least 5 years in a leadership role.
Manage sales order processing and coordinate dispatches Handle invoicing in the ERP system as per order and delivery status Process GRPO (Goods Receipt PO) entries to track incoming goods Manage the credit note process for returns, price discrepancies, or cancellations Follow up on back orders and communicate delivery timelines Maintain and share logistics MIS reports for orders, deliveries, and inventory Experience: Graduate in Commerce, or related field 2-4 years of experience in sales coordination or order processing Proficient in Excel Strong organizational and communication skills
Experience Key Responsibilities: Hands-on experience in aseptic processing of biological/pharma products, including sterile filling, sealing, and packaging. Skilled in operating aseptic equipment and ensuring compliance with GMP, GDP, ISO 13485, and Health Safety standards. Maintains strict hygiene protocols and controlled sterile environments. Proficient in environmental monitoring, aseptic area upkeep, and contamination control. Accurate documentation of batch records, QC logs, and processing reports. Strong foundation in microbiology and pharmaceutical standards, backed by B.Sc./M.Sc./B.Pharm/DMLT qualifications. 1-4 years of industry experience in aseptic manufacturing and sterilization.
Experience: Minimum 5+ yrs of MedTech sales with 2+ yrs of People Management experience. Expertise in Wound Closure products preferred. Strong leadership, communication, and negotiation skills. Proven track record of meeting or exceeding sales targets in the healthcare sector. Key Responsibilities: Manage corporate accounts, driving sales growth in the Hyderabad & Ludhiana region. Lead and mentor a team of sales professionals. Oversee sales of Wound Closure Products. Build strong relationships with surgeons, hospital administrators, and procurement teams.
Key Requirements: 3-5 years of experience in digital marketing Proficient in SEO, Social Media, Email & Paid Ad Campaigns Website and application management experience (WordPress/CMS) Strong grasp of design aesthetics and current global marketing trends Skilled in content creation, copywriting & performance analytics
To carry preventive and breakdown maintenance of entire plant machineries. Identify, troubleshoot and repair mechanical & pneumatic problems of plant equipment. Perform preventative maintenance per defined interval/schedule in a timely manner and document concerns. Maintain usage log of all utility equipment. Respond quickly to all service requests and efficiently repair breakdown. Work rapidly without compromising quality to minimize down times. Comply with all safety standards and regulations. Monitor spares inventory. Maintain a clean and organized work environment. Ensure 100% adherence to safety procedures. Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹30,000.00 per month Ability to commute/relocate: Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Required) Shift availability: Night Shift (Preferred) Day Shift (Preferred) Work Location: In person
Department - Clinical Roles and Responsibilities: End to End clinical data management and pertinent documentation for clinical studies and real-world data collection. Managing vendors for CDM Conducting User Acceptance Testing Provide guidance on training requirements in relation data management System and technical Skills Regulations and Standards 21CFR part 11, GDPR, ISO 27001, SDLC and ISO 62304, CDISC standards Databases & ORM: EDC databases - Clinion, OCRDC, Oracle one, Inform, Open clinica, etc. MS Access Tools: MS office, Power Automate, Power BI, MedDRA, WHODD, Rave, Clinion, Research Manager Understanding of the Medical Device industry
Role & responsibilities Participate in the investigator recruitment process. Perform initial qualification visits of potential investigators and sites. Evaluate the capability of the site to successfully manage and conduct the clinical study, both clinically and technically. Work with the Study Start-up Group to coordinate activities with the site in preparation for the initiation of studies. Obtain regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Perform study initiation activities, reviewing with the site study team the protocol, regulatory issues, study procedures, and provide training on completion of the e-CRF; monitoring activities and study close-out activities. Train site study team on the EDC system. Conduct periodic site file audits to ensure compliance with GCPs and sponsors standard operating procedures. Assure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Perform validation of source documentation as required by sponsor. Prepare monitoring reports and letters in a timely manner as per Clinical Trial Monitoring Plan. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture Document accountability, stability and storage conditions of clinical trial materials as required by sponsor. Perform investigational product inventory. Ensure return of unused materials to designated location. Review the quality and integrity of the clinical data through in house review of electronic CRF data and on-site source verification. Work with sites to resolve data queries. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Coordination with central and corelab (Echocardiography, QCA, OCT/IVUS, ECG) involved in the clinical trial. Review protocols, eCRFs, ICF and other related documents, as requested by Project Manager. Assist with final date review and query resolution through database lock. Online & offline regulatory/IEC submissions of different countries. Coordination with DSMB, Steering committee, CEC and attend meetings and prepare minutes of meetings. Preparation of study presentation for review meetings at Central Drug Standard Control Organization Regulatory Body of India. Preparation of Study presentation for national & international conferences.
Key Responsibilities: Bachelor s degree in Life Sciences, Business, or a related field (preferred). Strong knowledge of Endo Surgery products, market trends, and the surgical/OT environment. Proven ability to achieve and exceed sales targets in the medical device or healthcare sector. Promote and sell Endo Surgery products while identifying and developing new business opportunities. Build and maintain relationships with key opinion leaders (KOLs), healthcare providers, and procurement departments. Excellent interpersonal, communication, negotiation, and presentation skills. Execute sales strategies to consistently meet monthly, quarterly, and annual targets. Deliver product demonstrations and provide technical support.
At Advanced MedTech Solutions (AMS) , we are committed to excellence in manufacturing and ensuring a safe, sustainable environment for our teamsand we're expanding our operations! We're looking for a dedicated Safety Professionals to join our EHS team in Vadodara and help us maintain the highest standards of occupational health and safety. Location: Vadodara Qualification: Diploma in Occupational Health & Industrial Safety Experience: 4-8 years Key Skills: Knowledge of safety legislation & compliance (GPCB, ISO 45001) Hazard identification & risk assessment Fire safety management & mock drills Strong communication & problem-solving skills
Role & responsibilities Design and develop analog/digital/mixed-signal circuits for medical devices. Create and validate PCB layouts and component selections. Work with embedded firmware/software teams for system integration. Perform design feasibility, prototyping, and functional testing. Development of component specifications, inspection methods, bills of materials and manufacturing processes. Skills: Strong knowledge in analog/digital circuit design. Experience with PCB design tools (e.g., Altium, Eagle, OrCAD). Familiarity with microcontrollers, signal conditioning, sensors, power supplies. Knowledge of embedded systems and basic programming (C/C++) is a plus. Understanding of medical device standards (IEC 60601, ISO 14971, IEC 62304). Problem-solving mindset with hands-on debugging and analytical skills. Good communication and cross-functional team collaboration. Preferred Industry: Medical Device Education Qualification: B. Tech in Electronics & Mechatronics
Education Qualification B. Tech in Electronics or Mechatronics (Mandatory) Experience: 3-5 Years Key Responsibilities: Design and develop analog/digital/mixed-signal circuits for medical devices. Create and validate PCB layouts and component selections. Work with embedded firmware/software teams for system integration. Perform design feasibility, prototyping, and functional testing. Development of component specifications, inspection methods, bills of materials and manufacturing processes.
About Us: Advanced MedTech Solutions is a leading innovator and manufacturer of the medical devices, dedicated to improving patient outcomes through advanced healthcare products. We are committed to excellence and continuous improvement in all our operations. Position Overview: This role will oversee a team of design engineers, managing the end-to-end process of product design, development, and improvement. This role combines technical expertise with leadership skills to ensure innovative, compliant, and reliable product solutions. Key Responsibilities: Lead, mentor, and manage a team of design engineers to achieve project milestones and technical excellence. Drive the conceptualization, design, and development of new products and enhancements in line with business goals. Ensure designs comply with industry standards, regulatory requirements, and internal quality policies. Collaborate with cross-functional teams including R&D, manufacturing, procurement, and quality assurance to ensure seamless product development and launch. Oversee CAD modelling, prototyping, testing, and validation activities; optimize design processes for efficiency and Innovation. Manage project timelines, resources, and budgets while maintaining high standards for quality and innovation. Establish and enforce design review procedures, documentation standards, and change management protocols. Drive continuous improvement initiatives to enhance design quality, reduce time-to-market, and optimize costs. Eligibility: Bachelors degree in Electronics, Mechatronics, Electrical, or related Engineering field; minimum 5-10 years of relevant product development experience. Working knowledge of regulatory standards and design controls for medical devices (ISO 13485/ISO 14971/FDA guidelines) Bachelors or master’s degree in mechanical, Electrical, Product Design, or related engineering discipline. 8+ years of experience in product design and development, with at least 3 years in a leadership or managerial role. Proven expertise in CAD software (AutoCAD, SolidWorks, CATIA, etc.) and design validation processes. Strong knowledge of industry standards, regulatory requirements, and quality processes. Excellent project management, leadership, and communication skills. Ability to foster innovation, teamwork, and drive results in a fast-paced environment.
About Us: Advanced MedTech Solutions is a leading innovator and manufacturer of the medical devices, dedicated to improving patient outcomes through advanced healthcare products. We are committed to excellence and continuous improvement in all our operations. Position Overview: Seeking a Polymer Engineer with expertise in biodegradable polymers to design, develop, and optimize polymer materials for medical device applications. The role focuses on creating biocompatible, sustainable polymer solutions that meet stringent regulatory and quality standards. Key Responsibilities: Develop and characterize biodegradable polymer materials suitable for medical devices, ensuring biocompatibility and compliance with ISO 10993 and related standards. Design and optimize polymer synthesis, processing, and formulation to achieve targeted mechanical and degradation properties. Collaborate with cross-functional teams including product development, regulatory, and manufacturing to integrate polymer solutions into device designs. Establish and maintain robust testing and quality control protocols for polymer materials. Drive process development, scale-up, and manufacturing readiness of polymer-based components. Support risk assessment, documentation, and regulatory submissions related to polymer materials and processes. Investigate and implement sustainable polymer technologies to reduce environmental impact. Eligibility: Bachelors or masters degree in Polymer Science, Materials Engineering, Chemical Engineering, or related field. 3-5 years of experience in biodegradable polymer development, preferably for medical device or healthcare applications. Strong understanding of polymer chemistry, processing techniques, and material characterization methods. Familiarity with regulatory requirements and standards for medical polymers (ISO 13485, ISO 10993, FDA). Experience with synthesis methods, biodegradation testing, and analytical instrumentation (e.g., DSC, TGA, FTIR, GPC). Excellent problem-solving, communication, and teamwork skills.