We are looking for a Senior Engineer, working in the Pharmaceuticals & Medical Products industry in Irvine, California, United States.
Supports documentation control activities (QUMAS, FirstDoc, Coral)
Streamlines supplier quality activities within medical device R&D QA department
Verifies, completes, and maintains Approved Supplier List.
Creates and maintains change controls associated with suppliers
Evaluates qualification requirements and work with RDQA representatives to conduct and document qualification activities (including audits)
The pay range we are offering is 75 to 80 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors's degree in Engineering.
Excellent internal and external customer service skills
Strong attention to detail, good organizational skills and the ability to prioritize with changing situations
Ability to maintain confidential and sensitive information
Good interpersonal, verbal and written communication skills
Strong knowledge of Microsoft Word, Excel and PowerPoint and other computer applications
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.