JT112 - QUALITY ENGINEER I

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place
• Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment
• Designs or specifies inspection and testing mechanisms and equipment
• Conducts quality assurance tests
• Performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements
• May specialize in the areas of:
  • Design
  • Incoming material
  • Production control
  • Product evaluation and reliability
  • Inventory control
  • Research and development
• Applies these areas as they relate to product or process quality

Qualifications:

• Requires a Bachelor degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A))
• 1 year of experience required.
• Ability to support:
• Manufacturing process quality activities
• Investigations
• Validation deliverables
• Risk assessments
• Product/process performance monitoring
• Availability for 1st and 2nd shift