Quality Engineer II — Medical Device (Hybrid - Maple Grove, MN) Contract

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 www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp 

Our Fortune 500 Medical Device has an exciting opportunity for a Quality Engineer II 

Job Summary:

Develops, establishes and maintains quality engineering methodologies, systems, and practices which meet client, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. Provides focused quality engineering support within new product development, operational, or system/services support. 

Functional Engineering Roles include Design Assurance, Operations Quality, Software Engineering, Supplier Assurance, Product Analysis, Metrology, Microbiologist, Chemist. 
 
 

Key Responsibilities:

1. 1. Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. 
2. 2. Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. 
3. 3. Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices. 
4. 4. Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. 
5. 5. Assure in the development and execution of streamlined business systems which effectively identify and resolve quality issues. 
6. 6. Build Quality into all aspects of their work by maintaining compliance to all quality requirements. 

Qualifications

• 2 - 4 Years with BS 0 - 2 Years with MS 
• Med Device experience a plus 
• Schedule: 08:00:AM - 04:30:PM CST 
• Contract Length:12 months 
• Work Set-Up: Hybrid - Maple Grove, MN 
• Start Date: ASAP 

• Degree In Engineering

Other Details: