Actalent
US - Florida - Clearwater
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The role involves creating engineering documentation and designing production equipment to optimize manufacturing processes. Key duties include managing prototype builds and resolving design issues to ensure smooth production startup.
Requirements: Candidates must have a Bachelor's Degree in Engineering with over 5 years of experience, including at least 3 years in the medical device industry. Proficiency in process validation and history files management is required.
Key Skills: Process Development, Mechanical Design, Medical Device Engineering, Validation Processes, Engineering Documentation, BOM Management, Tooling Design, Quality Assurance Testing, Value Engineering, Prototype Management, Manufacturing Optimization, Process Validation
Benefits: Medical, Dental, Vision, Critical Illness, Accident, Hospital, 401(k) Retirement Plan, Life Insurance, Short And Long-term Disability, Health Spending Account (HSA), Transportation Benefits, Employee Assistance Program, Paid Time Off
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