JT112 - QUALITY ENGINEER I

Quality Consulting Group•Humacao, PR

About The Position

Quality Consulting Group is seeking a motivated Quality Engineer I to support work in the pharmaceutical, biotech, medical device, and manufacturing industries in Puerto Rico and the United States. The role develops and maintains quality standards and protocols for processing materials into partially finished or finished products, and works with engineering and manufacturing teams to ensure those standards are in place. It also involves designing or specifying inspection and testing mechanisms, conducting quality assurance tests, and evaluating product and production-equipment precision and accuracy. The position may apply quality practices to areas such as design, incoming materials, production control, product evaluation and reliability, inventory control, and research and development.

Requirements

  • Bachelor's degree, or for degrees earned outside the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).
  • At least 1 year of experience.
  • Ability to support manufacturing process quality activities, investigations, validation deliverables, risk assessments, and product/process performance monitoring.
  • Availability for first and second shifts.

Responsibilities

  • Develop, modify, apply, and maintain quality standards and protocols for processing materials into partially finished or finished products.
  • Collaborate with engineering and manufacturing functions to ensure quality standards are in place.
  • Devise and implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
  • Design or specify inspection and testing mechanisms and equipment.
  • Conduct quality assurance tests.
  • Perform statistical analysis to assess the cost of products or materials that do not meet required standards and specifications and determine responsibility for them.
  • Ensure corrective measures meet acceptable reliability standards and that documentation complies with requirements.
  • Apply quality practices to design, incoming materials, production control, product evaluation and reliability, inventory control, or research and development, as applicable.
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