Systems Engineer - Medical Device at Techtrueup

Newark, Delaware, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Jun, 26

Salary

0.0

Posted On

14 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Design Controls, Traceability, Design Validation, Design Verification, FDA Regulations, ISO 13485, User Needs, Design History File, Risk Management, Cross-Functional Collaboration, Documentation, Process Improvement, Problem-Solving, Analytical Skills, Medical Device

Industry

Human Resources Services

Description

Company Description Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition. Job Description Title: System Engineer - Medical Device Industry Location: Newark, DE Long Term Contract Job Overview: We are seeking highly skilled and experienced System Engineers to join our team. The ideal candidate will have 5-8 years of experience in the medical device industry, with a strong focus on Design Controls, traceability, and design validation. This individual will play a critical role in ensuring that user needs are clearly traced to design inputs, verification, and validation throughout the product development lifecycle. Key Responsibilities: · Design Controls: Lead efforts to develop and implement robust design control processes for new and existing products, ensuring compliance with FDA regulations (21 CFR 820), ISO 13485, and other relevant industry standards. · Traceability: Establish and maintain traceability throughout the design and development phases, ensuring that user needs, design inputs, and verification requirements are fully traced and documented. · User Needs to Design Validation: Work cross-functionally to trace user needs to design validation, ensuring that final products meet both the defined requirements and user expectations. This includes the development of comprehensive Design History Files (DHF) and validation documentation. · Design Verification & Validation (V&V): Collaborate with teams to ensure that all products undergo thorough design verification and design validation processes, providing evidence that the product meets the necessary specifications. · Cross-Functional Collaboration: Work closely with other engineering disciplines, such as hardware, software, and quality teams, to ensure a seamless integration of design controls and traceability throughout the product lifecycle. · Documentation and Reporting: Prepare and maintain detailed documentation for design control processes, ensuring all deliverables are compliant with internal and regulatory standards. Provide updates to leadership and stakeholders on project status, risks, and timelines. · Continuous Improvement: Identify areas for process improvements in design control and traceability methods, and implement changes that enhance the efficiency and effectiveness of product development. Required Qualifications: · Experience: 5-8 years of experience in system engineering within a regulated environment, preferably in medical devices or other highly regulated industries. · Design Controls: Strong experience in implementing and managing design controls processes, including traceability, user needs, and design verification/validation. · Traceability: Proven ability to ensure full traceability from user needs to design validation and manage product documentation accordingly. · Regulatory Knowledge: In-depth knowledge of FDA regulations (21 CFR 820), ISO 13485, and other applicable standards for medical devices. · Collaboration: Strong communication and interpersonal skills, with experience working effectively in cross-functional teams. · Strong verbal and written communication in English Preferred Qualifications: · Risk Management: Experience with risk management processes, including risk analysis, risk assessment, and mitigation strategies (e.g., ISO 14971). · V&V Experience: Familiarity with verification and validation techniques and methodologies for ensuring that product designs meet both functional and regulatory requirements. · Software and Tools: Experience with requirements management tools, traceability software, and common V&V tools. Personal Attributes: · Strong analytical and problem-solving skills · Ability to manage and prioritize multiple tasks in a fast-paced environment · Detail-oriented with a commitment to accuracy Proactive and able to work independently or as part of a team Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

The Systems Engineer will lead the implementation of robust design control processes, ensuring compliance with FDA regulations and ISO 13485 for new and existing medical devices. A critical function involves establishing and maintaining full traceability from user needs through design inputs, verification, and validation activities.