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We are looking for a highly motivated and experienced ISO/CE Documentation Specialist to join our team and help us maintain and improve our ISO and CE compliance.
Responsibilities:
Develop, maintain, and review ISO and CE documentation
Ensure that all documentation is up-to-date and compliant with all applicable regulations
Work with the engineering team to implement and improve ISO and CE processes
Conduct internal audits to ensure compliance
Provide training to employees on ISO and CE requirements
Qualifications:
English proficiency
Bachelor's degree in a related field
3+ years of experience in ISO and CE documentation for medical devices
Strong knowledge of ISO and CE standards and regulations
Excellent writing and communication skills
Ability to work independently and as part of a team
Benefits:
Competitive salary and benefits package
Opportunity to work on cutting-edge medical devices
Collaborative and supportive work environment
To Apply:
Please submit your resume and cover letter to us.
Why You Should Join Us:
We are a passionate team of engineers and scientists who are dedicated to developing innovative medical devices. We offer our employees a competitive salary and benefits package, as well as the opportunity to work on cutting-edge technologies that are making a real difference in people's lives.
If you are a talented and experienced ISO/CE Documentation Specialist who is looking for a challenging and rewarding opportunity, we encourage you to apply.
شرکت دانش بنیان مد فناوران پلاس از سال 1394 با رویکرد تولید تجهیزات پزشکی High tech و با بیس دانش شروع به کار کرد، این شرکت امروز توانسته است در حوزه تولید تجهیزات پزشکی گام بلندی را بر دارد و با تاسیس کارخانه خود در منطقه ویژه اقتصادی پیام کرج این مسیر را ادامه دهد. اکنون با تولید تجهیزات High tech تصویربردای در حال توسعه محصولات خود می باشد.
محیط شرکت، محیطی آرام، علمی و تحقیقاتی است که تمام پرسنل شرکت در بخش های تولیدی و تحقیق وتوسعه از فارغ التحصیلان دانشگاه های برتر کشور می باشند.