Engineer II Process – Controls

AbbottLiberty, SC
$61,300 - $122,700Onsite

About The Position

Performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations.

Requirements

  • Bachelors Degree (± 16 years) in Engineering or Technical Field
  • Minimum 2 years experience
  • 2 – 4 years manufacturing experience.
  • Experience designing and testing medical devices required.
  • Experience developing manufacturing processes and technologies and designing for manufacturability required.
  • Ability to work in a highly matrixed and geographically diverse business environment.
  • Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
  • Ability to leverage and/or engage others to accomplish projects.
  • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
  • Multitasks, prioritizes and meets deadlines in timely manner.
  • Strong organizational and follow-up skills, as well as attention to detail.
  • Ability to travel, including internationally.

Nice To Haves

  • Experience working in a broader enterprise/cross-division business unit model preferred.

Responsibilities

  • Establishes processes based on product specifications.
  • Evaluates process and design alternatives based on “design for manufacturability” principles.
  • Understands principles of “Cost of Goods Sold”.
  • Manages program compliance with “Quality Control” requirements (i.e. Design Control, Process validation etc.).
  • Understands IP issues relative to processes being developed.
  • Maintains knowledge of new developments in manufacturing and design technologies.
  • Understand work environment issues (i.e. OSHA regulations, etc.).
  • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
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