Medical Device Development Jobs in Arizona (NOW HIRING)

FREE TEMPLATE
Staff Quality Engineer - Product Development_Tempe, AZ_Full-Time(FTE)_Direct Hire
Hi,
Trust this finds you well!
We've spotted your impressive profile and have an exciting opportunity tailored to your skills and passions.
Position Title: Staff Quality Engineer - Product Development
Job Type: Full-Time
Location: Tempe, AZ
Base Salary: $110,000 to $115,000 + Best-in-class benefits
Industry: Medical Equipment / Devices
Job Category: Manufacturing - Quality
Job Responsibilities:
* Technical leadership skills including an understanding of medical device operations (e.g., medical device manufacturing, process development, quality assurance) and chemical and pharmaceutical operations (e.g., drug product manufacturing, analytical testing, process development and quality assurance)
* Ability to create, support, review, and investigate analytical test methods used to support pharmaceutical combination devices.
* The ability to create, support, review chemistry, manufacturing, and controls device submissions
* Participates as team leader or as an active member of the team to meet company objectives and ensure department responsibilities are completed
* Leads development of risk assessments and test method activities (e.g., development and validation for physical and analytical test methods)
* Leads component qualifications, design validation, design verification, drug stability and process validation
* Leads product investigations
* Ability to make and present risked based decisions
* Assess product changes against product design
* Supports translation of design inputs into manufacturing control plans
* Develop and implement procedures to comply with corporate and industry standards.
* Coordinates and/or directs all aspects of product development activity related to a product line
* Leads development of risk assessments and test methods
* Quality engineering representation on Product Development and Design Review teams
* Prepare and present project updates and technical discussions
* Participate in project planning, budgeting, scheduling, and tracking
* Support internal and external supplier audits
* Provide support to the regulatory department in writing technical submissions
* Complies with company procedures and policies, government regulations
* Actively participates in training and providing input to training of employees on division procedures and policies
* Ability to travel for business, project, and issues approximately up to 25% of time.
* Other duties and projects, as assigned
Required Education and Experience:
* BS in Engineering, Biological Science, or a related engineering field (Masters or Ph.D preferred). Fields of study include Chemical Engineering, Bioengineering, Pharmacy, or Biochemistry 
* Minimum of eight years of experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry
* Extensive proven understanding of design controls in development stage
* Pharmaceutical or combination product experience
Required Qualifications:
* Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)
* Ability to lead creation of risk management files
* Ability to develop solutions with business impact
* Advanced statistical and risk assessment techniques
* Working knowledge of test method (development and validation), equipment qualifications, process and design validation, risk assessment techniques, and component qualification methodologies
* Ability to make and present risk-based decisions
* Strong interpersonal skills
* Ability to analyze and optimize manufacturing and quality systems
* Product, design & prototyping
* Ability to create and provide training
* Problem solving ability
* Ability to create, review and coordinate test protocols and reports
* Ability to generate engineering proposals
* Oral and written presentation skills
* Ability to lead cross functional teams
* Understanding of regulatory requirements including ISO 13485, ISO 14971, 21 CFR 210/211/820 , ICH Guidelines
Skills and Certifications:
*Drug Device delivery combination products
Compensation:
*Full-time
*Benefits - Full
*Relocation Assistance Available - Possible for ideal candidate
Candidate Details:
*7+ to 10 years experience
*Seniority Level - Mid-Senior
*Minimum Education - Bachelor's Degree
*Willingness to Travel - Occasionally
Ideal Candidate:
*8+ years experience in New Product Development of combination devices
----------
Please follow our company LinkedIn page for future updates: https://www.linkedin.com/company/78708714/admin/feed/posts/
This guarantees that you'll receive real-time updates on roles that match your unique skills.
Happy connecting on LinkedIn, World # 1 Professional site