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Design & Development Manager-Medical Devices

10.00 to 18.00 Years   Delhi   25 Sep, 2020
Bee5 Manpower Consulting
Job LocationDelhi
EducationNot Mentioned
SalaryRs 7 - 12 Lakh/Yr
IndustryIT - Software
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

Designation: Design & Development ManagerReports to: Technical DirectorIndustry: Medical Devices (Class II & Class III Orthopedic Implants)Place of Posting: Sonipat 2 KM from Delhi Border (Singhu Border)Working Hours: 9:30 AM to 6:00 PM (Monday to Saturday)Duties and Responsibilities1. To create product design drawings, Product designing, Value engineering, reverse engineering of given products, fixtures, assemblies on various software platforms, like sold works etc.2. To make 3D Model for die punch, fixture & their assemblies with respective devices.3. New product development from idea or concept to market.4. To ensure compliance to various applicable internal procedures and international standards and guidelines for design and development activities such as ISO 13485, CFR etc.5. To Ensure smooth functioning and continual improvement in quality, delivering higher value services and productivity as per approved procedures.6. To Lead and accomplish projects end to end.7. To lead, manage, delegation, reporting of the team, Work distribution for team members and Nurture a positive work environment8. Cross functional liaison for projects and day to day activities.9. Continual process improvement activities for the department.10. All other tasks as assigned by the management. Key Skills: Design & Development, DHF, Medical Devices, ISO 13485, ISO 14971, Mechanical Engineering, Design Engineering, EU MDR, Auto Cad, Solid Works, Solid Cam, USFDA, MDSAP, CFR, 3D Model, Die Punch, Tool designing, NPD, Fixture, PSI, product designing, reverse engineering, value engineering, design drawings, MDD, FMEA, orthopaedic implants, orthopaedic instruments, design and drafting, R&D, D&D. Required Candidate profileDesired Candidate Skills and Qualifications:

  • Bachelors or Master s Degree in Engineering (highly preferred).
  • 10+ years of hands on experience software (AutoCAD, Solid works, MS-Office etc.)
  • Knowledge of U.S. FDA medical device regulations and standard requirements (ISO 13485/ISO 9001, ISO 14971, DHF, FMEA, EU Medical Device Directive
  • Excellent leadership, communication, collaboration, team work and interpersonal skills.
  • Superb ability to effectively communicate with staff members and business partners at all levels of the organization (both internal and external).
  • Excellent computer and internet search skills.
  • Strong ability to multi-task and to meet business deadlines.
  • Independent ownership of complete project deliverable, effective communication with cross functional team is required.
  • Good experience in programming (in solid cam software), Machine handling and tool management will be an advantage.
  • Excellent organizational skills with an ability to think proactively and prioritize work.
Key Skills: Design & Development, DHF, Medical Devices, ISO 13485, ISO 14971, Mechanical Engineering, Design Engineering, EU MDR, Auto Cad, Solid Works, Solid Cam, USFDA, MDSAP, CFR, 3D Model, Die Punch, Tool designing, NPD, Fixture, PSI, product designing, reverse engineering, value engineering, design drawings, MDD, FMEA, orthopaedic implants, orthopaedic instruments, design and drafting, R&D, D&D. ,

Keyskills :
auto caddesign engineeringiso 13485ms officesalesinsuranceproduct designrecruitmentdesign drawingscorporate liaisonproduct developmentprocess improvementrecruitingmechanical engineeringiso 14971solid worksreverse engineeringmedical device

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