DEKA is one of the leading research and development companies in the country and is the birthplace of some of the most innovative and life-changing products of our time$1. .$1
2 days ago
🏢 In-office - Manchester
DEKA is one of the leading research and development companies in the country and is the birthplace of some of the most innovative and life-changing products of our time$1. .$1
• Provide Quality guidance in a dynamic medical device environment. • Work cooperatively with cross functional design team members. • Participate and lead Risk Management activities. • Lead investigations including root cause identification and corrective actions. • Ensure the accurate documentation / recording of information. • Drive system and process improvements. • Participate in internal and external audits.
• Bachelor’s degree in an engineering or related STEM discipline. • Minimum 2-5 yrs. of recent professional experience (medical device experience is preferred) as QE in a regulated manufacturing environment. • Must be detail oriented and have strong communication both written and verbal. • Experience with compliance, with applicable standards and regulations such as 21 CFR 820, ISO 13485, and ISO 14971 is preferred. • Ability to: Multitask and carry tasks through to completion • Manage multiple sources of data and develop reports
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