Come Work With Us!
Magenta is a medical device company developing the world’s smallest heart pump, meant to provide minimally-invasive support to the heart during acute episodes of dysfunction. The Elevate™ System is multi-disciplinary, involving mechanical engineering, material science, electrical engineering, software, algorithms and state-of-the-art catheter fabrication techniques.
We are looking for the best people possible who can help us propel the Elevate™ System forward and save more lives.
We are looking for an energetic and positive Administrative Manager to join our HR team.
Reports to: Director of HR.
ResponsibilitiesIn this role, you will be responsible for all administrative tasks in the office:
• Office management and various administrative tasks related to operations, logistics, and facilities.
• Assist employees and visitors with travel arrangements, including flights and accommodation, and prepare expense reports.
• Maintain kitchen inventory, place supermarket orders, and manage office supplies.
• Assist with planning and execute various HR activities such as employee welfare, gift-giving, happy hours, holiday celebration, and company events.
• Address employee queries regarding office management.
• Provide general support to visitors.
• Provide administrative assistance to the CEO.
• Assist in the onboarding process of new employees.
• This is a temporary role for 8 months, serving as a maternity leave replacement.
Qualifications
• Minimum of 3 years of experience in a similar or relevant role – must
• Bachelor’s/master’s degree in a relevant field – must.
• Proficiency in Microsoft Office suite – must.
• Experience in a startup company – an advantage.
• Excellent communication and interpersonal skills, with a positive attitude and ability to work well within a team.
• Ability to work independently.
• Positive and proactive approach with a “can-do” attitude.
• Strong attention to detail and problem-solving skills.
We are hiring a Junior Configuration & Production Engineer who will be part of the leading team of the engineering department and will be responsible for leading and providing cross-functional support in configuration management projects.
Reports to: Engineering & Project Manager
Responsibilities• Responsible for leading and providing cross-functional support configuration management projects such as:
• Supporting and maintaining the Bill Materials (BOM) management.
• Building and controlling company’s configuration products, including DMR.
• Supporting and maintaining ECOs (Engineering Change Orders), including engineering documents, for example: drawings, models, and technical data within the PLM system.
• Technical engineering support for the production and QC department.
• Work closely with several departments, including R&D, Engineering, Operations, QA, and Product Management.
Qualifications• B.Sc. Engineer in mechanical/ biomedical/ materials science (or other relevant degree) – must
• Experience in CAD (Solidworks – model & drawings) – must.
• Fluent in English with excellent writing skills – must.
• Prior experience with product BOM (Bill of Material) and ECO (engineering change orders) – an advantage
• Knowledge and experience in PDM – an advantage.
• Strong organizational skills and attention to detail.
• Strong analytical skills.
• Excellent collaboration and communication skills.
• Self-motivated and proactive.
We are looking for an experienced Quality Assurance Specialist to join our QA Operations group and support the variety of activities related to QA Operations.
Reports to: QA Manager
Responsibilities• Lead QA Operations activities with regards to verifications/validations for an FDA reviewed complex, multidisciplinary, active investigational device.
• Lead and perform the Engineering Change Order (ECO) process from risk analysis through protocol approval.
• Verification, execution, and analysis of reposts until FDA-ready.
• Provide guidance to the R&D and Engineering teams on IQ/OQ/PV activities.
Qualifications• B.A. or B.S. degree in a technical discipline, such as Engineering or Science.
• 5+ years of relevant experience in the medical device industry.
• Previous experience with medical device verification/validations, ECOs, medical device statistics
• Working knowledge of medical device international standards.
• Ability to work independently with minimal work direction and in a cross-functional team environment.
• Fluent in English with excellent writing skills, effective written and verbal communication skills.
• Excellent computer skills, including a working knowledge of Microsoft Office applications.
• Strong time management abilities to ensure timely task completion.
• Detail-oriented.
We are looking for a Supply Chain Coordinator to join our Supply Chain Group.
Reports to: Supply Chain Manager.
ResponsibilitiesDesign and lead NPI processes such as:
• Open, track, and update work orders for production.
• Manage the supply chain schedule: collaborate with various teams to receive updates and schedules.
• Plan inventory levels according to the production plan.
• Set priorities for QC (receiving inspection).
• Coordinate production changes with line managers, R&D, and engineering team.
• Coordinate sterilization processes.
• Manage the supply chain schedule: collaborate with various teams to receive updates and schedules.
• Serve as the purchasing coordinator for R&D.
Qualifications• Bachelor’s degree in Supply Chain Management, Logistics Industrial Engineering, Business Administration, or a related field – must.
• Experience with ERP Priority – must.
• Fluent in English – must.
• Prior experience in logistics or supply chain coordination – an advantage.
• Excellent communication and interpersonal skills.
• Ability to work in a fast-paced and dynamic environment.
• Self-motivated and proactive.
We are looking for a V&V engineer to join our V&V team.
Reports To – V&V Team Leader
Responsibilities• Participate in testing activities of the mechanical and clinical aspects of the company products, with focus on V&V bench tests of products and R&D prototypes.
• Conduct product testing activities under defined conditions to verify/reject product specification using scientific methods.
• Perform product testing on items and components that are in R&D phase.
• Develop test methods to support the testing process throughout prototype development and assembly.
• Write protocols and reports detailing testing procedures and results.
• Support animal studies and experiments, including handling biological tissues and blood samples.
Qualifications
• B.Sc. in Biomedical Engineering or Biotechnology – must.
• Hands-on laboratory experience – must.
• Understanding of test protocols – an advantage.
• Experience in data analysis – an advantage.
• Ability to integrate written and verbal instructions, in both English and Hebrew.
• Capability to accurately collect, record, and report data.
• Attention to detail.
Don’t see the position you’re looking for? We would still love to hear from you!