What are the responsibilities and job description for the Quality Engineering Intern position at Werfen?
Overview
Werfen
Werfen, founded in 1966, is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. The Company’s business lines include Hemostasis, Acute Care, and Autoimmunity diagnostics, as well as Original Equipment Manufacturing. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.
Our North American Commercial Operations, as well as our Headquarters and Technology Center for Hemostasis and Acute Care Diagnostics, are based in Bedford, MA. Our Headquarters and Technology Center for Autoimmunity Diagnostics is based in San Diego, CA. Additionally, our Technology Center for Hemostasis and Blood Gas Reagents is in Orangeburg, NY, and our Technology Center for Whole Blood Hemostasis is in San Diego, CA.
Overview
Werfen’s San Diego Internship Program is a 10-week, full-time, paid assignment that takes place over the course of the summer and is open to undergraduate students who are currently pursuing a degree from an accredited college or university.
The Internship program has been designed to allow students to learn through hands on experience, providing an opportunity to blend textbook knowledge with practical experience. Students will contribute to the development of new or improved medical diagnostic tests and will be given the opportunity to work cross functionally with other departments to maximize their learning opportunities.
Responsibilities
Key Accountabilities
- Write quality system documents which comply with applicable regulations and standards
- Participate on process validation teams
- Work cross-functionally, as a key resource, to solve problems related to product or process quality issues; investigate non-conformances, identify root cause, and determine/implement appropriate corrective action plans
- Conduct risk and trend evaluations for product non-conformances
- Ability to prioritize urgent matters
- Other duties as assigned
Networking/Key relationships
- Manufacturing/Operations
- Manufacturing Engineering
- Regulatory Affairs
- Research and Development
- Biomedical Quality Control Lab
- Incoming Quality Control Lab
Qualifications
Minimum Knowledge & Experience required for the position
- Currently enrolled in a bachelor’s or graduate degree program with a minimum GPA of 3.0.
Skills & Capabilities
- Excellent written and verbal communication skills are required.
- Basic understanding of quality engineering principles including root cause investigation is desired.
- Basic understanding of current Good Manufacturing Practices (cGMP) & Good Documentation Practices (GDP) is desired.
- Basic understanding of metrology principles is desired.
Travel requirements
- No travel needed.
Acknowledgement:
The above statements are intended to describe the general nature and level of work being performed by the incumbent. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of this position.
I have read and understand the job description for my position. I agree to comply with the corporate compliance policy and all laws, rules, regulations and standards of conduct relating to my position.
I understand that this does not constitute or contain a contract or employment promise of any kind. Nothing contained herein modifies the at-will nature of my employment with Werfen.
www.werfen.com
