Medical device

Mechanical Engineer Medical Device/Technical Documentation/New Product DevelopmentMedical Device/Technical Documentation/New Product Development ONLY FRESHER CAN APPLY Experience candidates can not apply this job. URGENTLY REQUIRMENT IN POWER PLANT company only Fresher call- Degree, diploma, and electronics. Electrical, Mechanical salary-14900/-22000 /- call 09459944150 Responsibilities Analyze and interpret highly specialized technical information to compose detailed documentation and technical manuals. Conducts complex documentation and user needs analysis Assists others with technical interpretations and appropriate phrasing for document content

Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe. https://medicaldevices.freyrsolutions.com/

Operon Strategist is a medical device consulting companies which provides regulatory guidance to various manufacturers in the healthcare industry to ensure the strategic development of these manufacturers.

We “Cliniva Healthcare” are a leading Manufacturer and Exporter of a wide range of Hospital Equipment Manufacturers & Professional Hospital Supply,Medical Instruments, Urology Instruments, Laparoscopy Instruments And Hospital Medical instruments, Health Care instruments or healthcare facility required products Many More in India, US & UK.The warehousing facility has a large number of shelves, which are sequentially marked, so that we can place the packaged products in accordance with their categories. Visit For More: https://clinivahealthcare.com/ Address: G/57, Sahjanand business Park,Near Keshwam estate, Near S.P.Ring Road, Kathwada GIDC, Nikol, Ahmedabad-382430.

Manufacturing Engineer Medical Device/DFM/Quality Improvement Power plant Urgently Required Diploma / Degree / ITI Electrical, Mechanical, Electronics Only Fresher s Job can Contact Salary 10000/- to 22000 call 9736571884 Responsibilities for the Manufacturing Engineer Develops new and troubleshoots moderately-complex manufacturing processes and equipment Independently analyzes moderately complex product designs for Manufacture, Assembly and Serviceability. Designs, executes and documents moderately complex FMEA, process validation and testing in accordance with cGMP's. Generates practical, sustainable and creative options to solve problems and create business opportunities, while maximizing existing resources. Supports Plant wide initiatives through the writing, performing and analysis of various procedures and protocols: Validations, ECN, TSR (Test Summary Reports), Production and facility documents. Attends SIC (Short Interval Control)OEE(Overall Equipment Effectiveness) Project team meetings on a project-by-project basis in order to involve hourly associates on project teams Work closely with the QA department to reduce defects associated with equipment and production processes. Develops and manages the implementation of improvements projects.

Fresher job only fresher job only fresher Power plant job only fresher requirement call now diploma/ degree/electrical,mechanical, electronics, ITI all trades fresher hiring salary 22000 to 25000 hostel + canteen all facility More info CALL now 8988764828 Electrical Engineer Medical Device/Testing /Verification Responsibilities Responsible for testing hardware requirements at the sub-system level to support the electrical engineering team including Dry Run execution, update test cases, and execute test cases during formal verification using ALM Technical support and service, documentation ownership, verification deviations and root cause analysis required Expected to make suggestion on improvements based on recent technical knowledge Contribute to the planning and execution of components of the verification process Recommend design improvements Requirements

Our patient monitor is medical devices that are used to monitor the health of a patient. Patient Monitoring is one of the awe-inspiring technologies, the brainchild of advanced science that serves as a tool in taking care of millions of lives. Our patient monitor is medical devices that are used to monitor the health of a patient. Patient Monitoring is one of the awe-inspiring technologies, the brainchild of advanced science that serves as a tool in taking care of millions of lives. Package Includes: 12.1” TFT Color LCD Display. With Standard interface, Oxygen graph, tent graph, big character interface and view bed, convenient to observe. Finish all operations by keys and knobs. Maximum 8-channel waveform synchronous display. Display 7-lead ECG waveform on one screen, cascade ECG waveform display. Standard Parameter: SpO2 NIBP ECG RESPIRATION TEMPERATURE Contact Us: Medicosys Pvt Ltd, Behind BSNL Tower,Sindagi Road,Indi, Dist: Bijapur, Vijayapura, Karnataka - 586209 Email: show contact info Phone: 7020208763 Website: https://www.medicosys.in/

Position: Sales Manager Qualification: MBA/Graduate Location: Ludhiana (Local Candidate Preferred) Experience: Minimum 1-3 years’ experience in sale of Medical Devices, Surgical Disposables, Critical, Cardiac, Urology, Surgery Etc.. Candidates should have very good contacts with doctors/hospitals. He should have very good knowledge of local market. He should have very good communication skills. He should be hard worker, Simple but enthusiastic. For Details, Contact: Bhatia Consultancy Services Punjab

Diploma / Degree - Mechanical with minimum 5 - 10 years of experience in related field. Knowledge of electrical circuits, PLC operations, HMI, Automation is preferred. Planning and undertaking scheduled maintenance. Responding to breakdowns. Diagnosing faults and repairing equipment. Supervising engineering and technical staff. Managing stocks of supplies and equipment. Ensuring smooth running of Prime Placement and Manpower Services We are Leading Placement Consultant in Ahmedabad. We require Production & Maintenance Engineer for our Client a Leading Manufacturing Company Located at Changodar - Ahmedabad - Gujarat.machinery. Quick learner. Email@vinod@primeplacement.in / primeplacementadi@gmail.com T.no:7777981967

Urgently we need candidates for our MNC Company in Chennai requires Sales & Marketing Executive Qualification – Any graduate Skills: Excellent Communication Skills with Good Contacts Minimum 2 + year Experience in Medical Equipment Device Sales or Marketing can apply Gender – Male Salary not an Constraint Job Location –Bangalore/ Kerala/Kolkata Interested candidates kindly send your resume here ; with your details Recent photo, Current CTC & Expected CTC, Notice period etc *Before send your mail please mentions in the subject which post you have to apply. Regards VC CONSULTANCY SERVICES No -7, iyyanar koil st, New Bus Stand Back Side, Land Mark: Opp to Samsung mobile service showroom Pondicherry -.

To generate sales through regular doctor visit as defined in the doctors list Responsible for device/product detailing with customers for prescription generation Effective planning for territory coverage to maintain healthy secondary to primary sales ratio Conduct CMEs and activities as defined in cycle meetings Monitoring the stock levels with the stockists, ensuring liquidation of stocks Timely reporting of daily work through sales force reporting system. Providing feedback to HO on sales figures, activities, competition etc.

ISO 13485 Certification works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. ISO 13485 Certification works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. Stakeholders' confidence will build strength in manufacturers and service providers. This standard acts as a building block for quality management. This certification is not a requirement of the ISO standard like other ISO management system standards have. Without going through the certification process an Organization can reap the benefits by implementing the standard. Stay tuned with us to know more Insight on this standard and also please visit our website www.ursindia.com to know more about other standards. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Mobile: +91-9650807813

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ISO 13485 Standard clauses and requirement are applicable to all types of organizations irrespective of size or nature and applicable to all like Hospital, Health Care, Trading, Manufacturing, Service Companies, Software, Construction, and Medical Devices in India. URS offers ISO 13485 Certification in all cities, in Mumbai India. ISO 13485 certification for Medical Device has been developed so that the medical industry does not compromise with public safety and health. This certification ensures that the companies follow all the measures to produce quality products as per the global standards. Stay tuned with us to know more Insight on this standard and also please visit our website www.ursindia.com to know more about other standards. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Mobile: +91-9650807813

ISO 13485 - Quality Management System in Solan clauses and requirement are applicable to all types of organizations irrespective of size or nature and applicable to all like Hospital, Health Care, Trading, Manufacturing, Service Companies, Software, Construction, and Medical Devices in India. ISO 13485 Certification in Noida works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. Stakeholders' confidence will build strength in manufacturers and service providers. This standard acts as a building block for quality management. This certification is not a requirement of the ISO standard like other ISO management system standards have. Without going through the certification process an Organization can reap the benefits by implementing the standard. Stay tuned with us to know more Insight on this standard and also please visit our website www.ursindia.com to know more about other standards. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Mobile: +91-9650807813

Mechanical Engineer Medical Device/Technical Documentation/New Product Development ONLY FRESHER CAN APPLY Experience candidates can not apply this job. URGENTLY REQUIRMENT IN POWER PLANT company only Fresher call- Degree, diploma, and electronics. Electrical, Mechanical salary-14900/-22000 /- call 09459944150 Responsibilities Analyze and interpret highly specialized technical information to compose detailed documentation and technical manuals. Conducts complex documentation and user needs analysis Assists others with technical interpretations and appropriate phrasing for document content

Are you at Risk of Heart Attack- Sibia Medical Centre Heart disease is the leading cause of death in India. The term “heart disease” refers to several types of heart conditions. The most common type is coronary artery disease, which can cause heart attack. Anyone, can develop coronary artery disease. It occurs when a substance called plaque builds up in the arteries. When this happens arteries can narrow over time and reducing blood flow to the heart. Increasing age, smoking, eating unhealthy foods, not getting enough exercise, high cholesterol, high blood pressure or diabetes can increase risk for heart disease. Anyone above 40 years or having these risk factors should undergo annual cardiac check. Besides Electrocardiogram, Treadmill test, Coronary CT angiography, etc. now a new device called Cardiovascular Cartography (CCG) is available to evaluate cardiac status. Cardiologists may become increasingly depend to diagnose heart ailments non-invasively with CCG’s 3D map heart flow map. CCG is a technique for early detection of coronary artery disease (CAD) to evaluate the functional status of the heart and plan further treatment. For CCG test the patient is "wired" to CCG device using electrodes and a highly sensitive transducer while the patient is lying down. If required the test can be repeated after a drug to see effect of mild stress on the heart. CCG can also be used to evaluate a drug’s effect on the heart’s function. Within minutes of giving a tablet of sorbitrate the redistribution of blood flow to the heart muscle is shown by the CCG. A high-speed computer makes all calculation and result is available within 15 minutes. Such data was earlier not possible through non-invasive methods. The records obtained include details such as the amount of blood pumped for every beat of the heart, pressure, volume and time relationship, relative oxygen demand, and much more. The CCG heart blood flow map has a positive predictive accuracy of over 90 per cent and a negative accuracy of over 80 per cent in detecting heart disease. Angiography measures the quantity of blockages in the heart’s blood vessels but not the amount of blood reaching the heart muscle. While angiography tells us how much water is flowing in the river, CCG tell us the quantity of blood reaching the fields. What is more important? For the farmer the quantity of water actually reaching his crops is all that matters. He is not concerned with the how much water is there in the river. Blockages in the arteries are not the only factor deciding how much blood reaches the heart muscles. Angiography does not tell us how well the body has compensated itself for the decrease in blood flow caused by the blockages. This compensation attributed to collaterals, pressure changes, etc. is not well assessable with angiography. This is why we often see patients with 99 percent blocks moving around without chest pain or heart attack. It is gradually being realized that blood flow to the heart muscle is all that matters. It is decreased flow to the heart muscle that causes angina chest pain or heart attack. CCG’s painless mapping of the heart blood flow is an important tool to detect coronary heart disease early, to evaluate extent of disease or to know the effectiveness of a treatment. It is often used to evaluate, plan and study progress of non-invasive, non-surgical treatments such as Artery Clearance, Chelation Therapy, Ozone Therapy, External Counter Pulsation, Extracorporeal Shockwave Myocardial Revascularization. (SibiaMedicalCentre.com)

Clinical Data Management Internship Opportunity: Get Hands On Experience On Oracle Clinical 4.6.6 & Oracle Inform Central Designer: Organization at a Glance: Gratisol Labs is a leading resource consulting services organization for the Pharmaceutical, Biotechnology and Medical Device industries. We offer contract and permanent job opportunities within the Pharmaceutical, Biotechnology and Medical Device industries to both experienced professionals and entry level candidates. The services offered fall into the broad categories of Recruitment Solutions, Temporary Staffing, Outsourcing, Consulting, Application Training in Clinical Data Management (Oracle Clinical, Oracle Inform/Central Designer), Pharmacovigilance (Oracle Argus Safety Database, Oracle AERS), CDISC SDTM & SAS to aspirants of Clinical Research Industry. We successfully help some of the top Pharmaceutical, Biotechnology and Medical Device organizations from around the world to recruit high caliber experienced & trained professionals. The focus of the lectures will be mainly on the following topics: » Introduction to Clinical Research & Clinical Data Management » Fundamentals of Clinical Research &Roles in a CRO » Clinical Data Management Process and Life cycle. » ICH GCP guidelines » Protocol Designing » CRF /e CRF Designing » CRF Annotation » DCF Management » Electronic Data Capture and Remote Data Capture. » Management of Medical Dictionaries(MeDDra, WhoDD) » Query management(DCF management) Coding » External data managing (e, g: Lab data, ECG, BMD etc.) » Clean Patient Delivery » Database Lock, Freeze. » SAS data Extracts Mode of training- Instructor Led Class room/ Online Training Practical Training will be also provided on Oracle Clinical 4.6.6 on the following topics: » eCRF Design » Data Entry » Discrepancy Management » Batch Validation Contact Information Gratisol Labs, KVREnclave, 2nd Floor,207,Ameerpet, Beside Satyam Theater,Hyderabad Mobile Number:

We provide consultation for Medical and In-vitro Medical Device CE, US FDA, NIOSH, ISO, and Indian MDR certification along with services like Appointment of Authorized Representative, External testing services, EUDAMED registration, UDI Labelling, Registration on Sugam portal, Country registrations, Internal Audits, Management Review Meetings, Training, GAP analysis & audits, Mock audits, Conformity assessment, Document review, and Audit NC closures. For clients who face limited challenges in specific documentation, we also provide a customized service of preparing individual documents or parts of it. Our training & consulting support helps medical device customers to design & manufacture their products in compliance with regulatory requirements and bring them to the market more quickly, effectively & efficiently.

Philips Respironic Oxygen Concentrator in absolutely new condition. Bought on January and used only for 3 months for a COPD patient in home. Warranty exist till January . Device would be sold with all original invoice and product certificate. The device produces concentrated oxygen from room air for delivery to a patient requiring low flow oxygen therapy. Most oxygen concentrators have been bulky, heavy, and require ongoing maintenance by patients and home care providers. But the 5-liter per minute Ever Flo stationary concentrator from Respironics has a unique set of features to lower the costs of providing oxygen therapy while maintaining ease of use for patients. That is why we chose to buy the best brand. It is totally hassle free and user friendly. The patient gets relief faster than manual oxygen cylinder as we compared it our-self. Following are the features: *Lightweight and easy to transport at 14 kilogram. *Compact, ergonomic design takes up less space, looks less like a medical device *One of the quietest mainstream concentrators *No home care provider filter change for two years *Uses less power and produces less heat, so it’s more patient-friendly *No filters for the patient to change *A recessed flow meter helps reduce the chance of accidental breakage. *EverFlo’s durable metal cannula connection is less likely to break. *Humidifier Bottle Platform is designed to be compatible with all bottle styles and features an easy-to-use velcro closure. The device has the following accessories: -Air Inlet Filter -Humidifier Connector Tube

BISI World was founded in April, 2019 with focus on 'Medical Equipment supplier in India' to 'bridge the information gap'on existing, innovative and costeffective devices. "Buy N95 Face Mask Online" BISI World is an “Medical Equipment supplier in India”. Our Business associates comprise of Hospitals, Doctors, MNCs, manufacturers, bulk suppliers/wholesalers/importers, Authorised dealers and sub dealers. We believe that our platform can create a 'conducive ecosystem for medical device sector' by opening up new avenues for trade of the medical devices. "Buy N95 Face Mask Online"

ISO 13485 QMS is specifically for medical devices and to provide much advantage for organization. This standard provide evidence to represent customers, organization follows global quality standard for manufacturing and designing of medical devices. ISO 13485 Certification works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. Stakeholders' confidence will build strength in manufacturers and service providers. This standard acts as a building block for quality management. URS offers UKAS and NABCB accredited ISO Certification services in all over India. If you are looking and interested to any ISO 13485 Certification, then Contact us for more information or visit URS website: URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Tel: 91-120-4516264 - 65 Mobile: +91-9650807813

We are looking for Marketing Executive for MNC Company, dealing in medical devices. Fresher or experienced 1-2 year in medical device or in pharma industry may prefer. Male or Female can apply.

ISO 13485 Standard clauses and requirement are applicable to all types of organizations irrespective of size or nature and applicable to all like Hospital, Health Care, Trading, Manufacturing, Service Companies, Software, Construction, and Medical Devices in India. URS offers ISO 13485 Certification in all cities, in Mumbai India. ISO 13485 Certification works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. Stakeholders' confidence will build strength in manufacturers and service providers. This standard acts as a building block for quality management. This certification is not a requirement of the ISO standard like other ISO management system standards have. Without going through the certification process an Organization can reap the benefits by implementing the standard. Stay tuned with us to know more Insight on this standard and also please visit our website www.ursindia.com to know more about other standards. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Mobile: +91-9650807813

The ISO 13485 is a certification measure that is like ISO 9001 but basically acts as a standard to measure best management practices in the health sector. ISO 13485 is an international standard intended to reassure organizations purchasing and utilizing medical devices that the developers and suppliers of these devices have instituted and implemented a QMS that meets certain minimum requirements, Suppliers and developers express their conformity and assurance to this level of medical device quality by becoming ISO 13485 certified. If a company or entity participates in or provides design and development, production, storage, distribution, installation, servicing or other technical support, their related operations most likely fall under the QMS standard. For more information and updates in the ISO 13485, keep an eye on the URS website. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Tel: 91-120-4516264 - 65 Mobile: +91-9650807813

Description: wanted for Regulatory Affairs Engineer Company: EDM SOFTWARE SOLUTION Location: Coimbatore, Tamil Nadu, India Description: EDM SOFTTECH SOLUTION PVT LTD COMPANY COIMBATORE 9791684242 Job Description: Company: Medical Equipment Manufacturing Industry Qualification: BE/Dip Mech Designation: Regulatory Affairs Engineer Exp: 4-5yrs Salary: 25-30k Location: Sulur, Coimbatore Skills: QMS Module, ISO documents and Medical Device field added advantage Skills: - Basic Skill - Communication Skill - Field Skill Fresher & experienced candidate both can apply Processing Time: 85 - 95 working days If you are interested kindly send your updated CV or contact us for more details Thanks and regards EDM SOFTTECH SOLUTIONS PVT LTD COMPANY COIMBATORE HR NO: 9791684242 / 9994241641 Email ID: edmsofttech@gmail.com

What Is Feeding Tube Replacement Services Feeding tube replacement services refer to medical care provided to individuals who require the replacement of their existing feeding tube. A feeding tube is a medical device that is inserted through the nose, mouth, or abdominal wall into the stomach or intestines to provide nutrition or medication to individuals who cannot consume food or liquids orally. The need for a feeding tube replacement may arise due to various reasons, including blockage, dislodgement, or malfunction of the existing tube. Replacement services may involve the removal of the old tube and insertion of a new one, as well as the evaluation of the patient's overall health and nutrition needs. Feeding tube replacement services are typically provided by healthcare professionals, such as nurses, doctors, or trained caregivers, who have expertise in managing patients with feeding tubes. These services are essential for individuals who depend on feeding tubes for their nutritional needs and can help to prevent complications and improve their overall quality of life. Read more: https://webhitlist.com/profiles/blogs/feeding-tube-replacement-and-complications #Feedingtubereplacementservices #woundcaresurgeon #feedingtubereplacement #Replacementservices

Dear ALL, Thank your for your interest in Our training services. Please find the Information & Brochure Attached. Pharmacovigilance Training in Oracle Argus Safety Database 8.0 Organization at a Glance: Gratisol Labs is a leading Contract Research organization providing full range of Clinical Research, Clinical Data Management, CDISC SDTM, Pharmacovigilance & SAS training Services to Healthcare Organizations globally. The Class room Training will be conducted at 'GRATISOL LABS', premises Kvr Enclave 2nd Floor 207,Ameerpet, Hyderabad from with hands on 100% practical training with real time case scenarios and live project for all the courses. Oracle Argus Safety Database Oracle Argus Safety is an advanced and comprehensive adverse events (AE) management system that helps life sciences companies enable regulatory compliance, drive product stewardship, and integrate safety and risk management into one comprehensive platform. Argus Safety is industry-proven and accepted, having been used for more than a decade at leading pharmaceutical, biotech, CRO, and medical device manufacturers. We offer instructor led online training. Classroom training's are conducted in Hyderabad, India. We also arrange corporate training's if group of people are interested from the same organization. Mode of Training- Classroom Course Fee: Rs you have to pay in two installments Batch Starts: 3rd August Classroom Timings: 8:15 Am - 9:30 Am Oracle Argus Safety Database Access (24/7 for 1 month) - During the training period (1 month), you will be provided access to the Oracle Argus Safety Database application server by a Username Password. You can log-in and practice in the lab. Let me know your interest to join and become an expert on Oracle Argus Safety Database. Please feel free to contact undersigned for any queries. Please conform the acceptance through this mail if you are attending this batch. Eligibility Applicants are recommended to have one of the following life Science degrees: Bachelor's, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital. Certification Certificate will be provided for this course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by Gratisol Labs. For more information/demo class, please contact Gratisol Labs at . Contact Details: Sanah Fatima Training Coordinator +91 Gratisol Labs KVR Enclave, 2nd Floor, #207, Ameerpet, Near Satyam Theatre, Above ICICI Bank, Ameerpet, Hyderabad. Contact No: Ph:040-(D), , Cell: +91 , E: mail: Website: www.gratisol.com

Quality Engineer Product Development/Consumer Goods/Design / Manufacturing Urgently required fresher Electrical, Mechanical, Electronics, Civil Fresher Candidates Only POWER PLANT JOBS Call 9805554116 *Note: Completion of a satisfactory criminal record check, eduacation verification, resident verification, id proof verification and reference checks are required prior to employment. Responsibilities Review product design for quality improvement opportunities and manufacturing ease. Lead New Product Development DFMEA s for all New Product Development. Owner of test plan, product qualification and Six Sigma tools during NPDP. Lead Risk Assessments during the product development cycle. Requirements Bachelor of Science Degree in Engineering 0-1 Years of related Quality Engineering experience in an R&D or manufacturing environment. Analytical Statistics Cp/CpK, ANOVA, DOE, Measurement Systems Analysis, etc Experience with experience with medical device consumer products, mechanical parts, components and assemblies such as castings, sheet metal, gears, plastics, etc. Reliability Testing and Analysis ASQ, CQE & Six Sigma: Green Belt/Black Belt certification(s) are a plus.

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