The Role
Leads and owns complex manufacturing engineering tasks within a technical discipline. Responsibilities include setting direction, identifying and resolving issues, developing creative solutions, coordinating with peers, and supporting verification and validation activities. The role requires knowledge of manufacturing operations, equipment validation, documentation, process implementation, and business objectives.
Summary Generated by Built In
Associate Engineer with knowledge of technical skills and understanding of the business objectives, manufacturing operations and dynamics of the company environment to take an effective and proactive leadership role in a specific technical manufacturing discipline. Set direction for, lead, and take ownership of complex manufacturing engineering technical tasks that may have multiple inter-coordinating elements. Will be able both to anticipate and identify key issues and make recommendations for resolution where precedent may not exist and creative thinking is required. Resolution may involve the application of new methods and approaches and may require the consideration of impact with other system components. Interaction with peers and mentors on the individuals' projects is generally in the context of peer review to confirm the rationale for task approach direction as well as peer review of verification/validation activities.
Requirements
- Bachelor’s Degree in Chemical, Industrial or Mechanical Engineering
- 0-2 years of relevant experience in Quality Manufacturing or Supplier Quality Engineering, preferably in the medical device industry.
- Bilingual (Spanish/English)
- Knowledge with equipment validation, documentation, and process implementation.
Skills Required
- Bachelor's degree in Chemical, Industrial, or Mechanical Engineering
- 0–2 years of relevant experience in quality manufacturing or supplier quality engineering
- Bilingual proficiency in Spanish and English
- Knowledge of equipment validation, documentation, and process implementation
- Experience in the medical device industry
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The Company
What We Do
QRC Group specializes in providing expert consulting services in regulatory compliance, quality management, and risk management for the pharmaceuticals, medical devices, biotechnology, and other regulated industries, delivering comprehensive project management and validation solutions.
