Job Role : R&D Engineer III
Overview:
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at
O ur Fortune 500 client has an exciting opportunity for R&D Engineer III.
Job Summary:
Work with R&D Design project teams to develop and execute plans to create, verify, and validate new technology , products, materials, processes, or equipment with minimal supervision. Understand internal and external requirements, facilitate team achieving deliverables on schedule, and drive recovery efforts when project impacted . Foster collaborative and communicative environment among team and cross-functional groups.
Responsibilities and Job Requirements:
1. Work with R&D Design and cross-functional partners to generate and execute on project plans.
2. Track, document, and communicate success criteria, dependencies, and work progress.
3. Identify and mitigate project risks and escalate issues as necessary to ensure success.
4. Support technical work through change notices, materials management, etc.
5. Facilitate SOP/WI compliance, design reviews, risk assessments, and verification/validation activities.
6. Drive continuous improvement initiatives to enhance team performance.
7. Help build a positive and engaged project culture.
8. Identify and track Design team's project budget needs.
Quality Systems Duties and Responsibilities:
Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
Qualifications
If 5-8 y ears of R&D Experience, candidate should have B achelor's Degree in Engineering .
If 3 - 6 years of R&D Experience , candidate should have M aster's Degree in Engineering
If 3 - 6 years of R&D Experience , candidate should have PhD .
Additional Job Specific Requirements:
• Strong MS Excel skills
• Good knowledge of medical device requirements, change notices, and D FMEA r equired .
• Familiarity with task management systems (MS Project, Jira, Miro, etc.) a plus.
• Must be proactive and able to drive execution with a positive and supportive approach.
Other Details:
Schedule: 06:00:AM - 02:30:PM EST
Contract Length: 12 months
Hybrid Set up at Arden Hills, MN
