Iso 13485 Jobs in Dhaka

Please share your resumes at Job Role: Manufacturing Engineer Location: Foxborough MA Contract: W2 Responsibilities: Design processes specify equipment develop work instructions conduct validation (IQ OQ PQ) and train production staff. Create validate and deploy More...

Bachelor’s degree in Life Sciences, Engineering, Technical Writing, or a related field; advanced degree preferred Minimum of 6 years of experience in regulatory writing, preferably within the medical device industry Strong understanding of regulatory requirements and guideli More...

Position Summary: We are hiring a highly dedicated QA/RA Manager who will manage all quality matters in the company and act as the Management Representative as defined in the ISOCFR Part 820 (FDA cGMP) Regulation (EU) 2017/745 or any other relevant standards and regulations.Job Respo More...

Position Summary: We are hiring a highly dedicated NPI Engineering Manager who will oversee and manage all Project Management and NPI activities on in the company.Job Responsibilities: Taking the necessary action to ensure that the standards related to ISO 13485 GMP product ISO stand More...

Position Summary: We are hiring a highly dedicated NPI Engineering Manager who will oversee and manage all Project Management and NPI activities on in the company.Job Responsibilities: Taking the necessary action to ensure that the standards related to ISO 13485 GMP product ISO stand More...

Role: Senior Quality Systems Specialist Location: Illinois Duration: Permanent Salary: $110000$115000K Job Description: We are establishing a new department and seeking an individual to join our team as a Senior Quality Systems Specialist in a manufacturing company specializing i More...

We Vivalyx are a medical technology startup from Aachen dedicated to saving people suffering from organ failure. Our goal is to significantly increase the vitality and number of donor organs. The company is currently in the preparation phase for certification and the associated studie More...

Job Title: Quality Systems Program Manager Client: Medical Device Manufacturing Company Duration: 7 months contract with possible extension Location: Northridge CA 91325 Shift: 1st Shift Job Description: Experienced project manager in the medical device industry responsible for inspec More...

Job Title: Quality Systems Program Manager Client: Medical Device Manufacturing Company Duration: 7 months contract with possible extension Location: Northridge CA 91325 Shift: 1st Shift Job Description: Experienced project manager in the medical device industry responsible for inspec More...

Job Title: Packaging Engineer Location: On site Grand Rapids MI (Must be local) Length: 12 year contract Musthaves Minimum 5 YOE in packaging Experience in packaging FFS equipment process development and validation IQ/OQ/PQ Experience in manufacturing environment process or man More...

Neurosoft Bioelectronics situated in Geneva Switzerland is at the forefront of medical equipment manufacturing specializing in innovative solutions for interfacing with neural tissue. Our mission is to revolutionize the treatment of severe neurological disorders such as epilepsy tinni More...

Job Title: Principal Engineer Software Verification & Validation Responsibilities: Provide leadership to effectively define communicate and execute test strategies to ensure product quality and delivery are maintained. Lead and collaborate with verification team to dri More...

Zoot Systems is a New Delhi India based company. For years it has been our continuous endeavours to understand Client qualityconscious discerning business needs and to successfully meet those. We specialize in the creation of highquality I.T./NonI.T. based HR Solutions Recruitment and More...

Mandatory Skills: Systems Engineering for Electromechanical Medical Devices InCose certification ISO 13485 ISO 14971 IEC 62304 Usability for Medical devices Regulatory for Medical Devices Requirements Management Jira IEC 606011 and any Particular standards. Overall technical leade More...

greenteg AG develops produces and markets cuttingedge thermal measurement solutions for life sciences and IoT sectors. Operating globally from our headquarters in ZurichRmlang our dynamic and international team serves a diverse clientele.We are seeking a Quality Engineer specializing More...

Position Responsibilities Support the Vice President RAQA to develop best practices for Enlitic regulatory and standards compliance.Assess procedures processes and organizations for compliance with GMP ISO 13485 EU MDR (2017/745) MDSAP Canadian MDR etc. standards and regulations.Work More...

Job DescriptionWe are seeking a highly skilled and experienced System Architect to lead the design and development of innovative medical devices. The ideal candidate will possess deep knowledge of medical device systems regulatory requirements and a proven track record in optimizing c More...

Job Title: EngineerLocation: A medical device client in SingaporeDepartment: EngineeringReports to: Engineering ManagerPosition Summary:My client is seeking a highly skilled and innovative Engineer to join our team in the medical device industry. The Engineer will be responsible for d More...

Job Title: Sr Packaging Engineer Exempt 13811 Location: Grand Rapids MI 49504 Duration: 4/15/2024 4/14/2025 Education Required: Bachelor of Science Degree in Packaging Science Mechanical Engineering or similar discipline Years Experience Required: Minimum of 5 years in med More...

Role: Sr System Engineer Location: Pittsburg PA Onsite Duration: Fulltime / Contract 2 POSITIONS Job Description: Mandatory Skills: Systems Engineering for Electromechanical Medical Devices InCose certification ISO 13485 ISO 14971 IEC 62304 Usability for Medical devices Re More...