Quality Engineer
BioPharma Consulting JAD Group
Houston, texas
Job Details
Contract
Full Job Description
BioPharma Consulting JAD Group has a great Associate Quality Engineer with an industry leader working on site in Houston, Texas.
Job Details:
- Review and approve quality systems control document.
- Review and approves process validation, V&V deliverables, environmental monitoring, risk management, documents and change requests.
- Assist in root cause investigation, CAPA implementation and effectiveness review. Serving as Quality contact for nonconforming product investigation and CAPP or both internal and external sources
- Participate in a variety of projects serving as quality voice and ensure project is progressing per company, regulatory, authority and industry requirements.
- Serving as quality voice for projects and tasks related to sterilization, environmental monitoring, cleanroom design and operation, laboratory management and endotoxin
- Complies with all policies and standards.
- Works under general direction, seeks assistance as needed
- Completes work in accordance with established procedures and practices within field of technical/scientific knowledge
- Establishes approaches for completing assignments
- Work requires consistent exercise of discretion and independent judgment
- Works with team to support achievement of project milestones
- Builds productive internal/external relationships
Preferred Qualifications:
- Experience in medical devices industry as Quality representative with review and approval process validation, V&V deliverables, environmental monitoring, risk management, documents and change requests. Root cause investigation, CAPA implementation and effectiveness review experience.
Education:
Bachelor's degree in Science or Engineering with 2-4 years of directly related experience
Requirements