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:
- Engineer will help with the Packaging Excellence (PEx) initiative. This initiative was generated to upgrade our sealers with Advanced Controls to have better control of process parameters. Subsequently the equipment needs to be validated for our packaging operations
- Designs, develops, analyzes, troubleshoots and provides technical skills during research and/or product development.
- Under the direction of the Engineer Section Head, provides technical direction to department engineers.
- Plans and coordinates larger scale engineering projects or several medium or small projects while acting as a technical specialist for a specific section. Maintains a thorough knowledge of new developments and technology.
- Monitors projects and recommends changes to improve operating efficiency.
Qualifications:
- Bachelor Degree in Engineering.
- Four (4) year of previous experience in Medical Device or Pharmaceutical Industry.
- Experience in Equipment validation, FDA Compliance and Statistical Analysis
- Knowledge of Master Validation Plan (MVP), Defining Document (DD), Installation Qualification (IQ), Measurement System Analysis (MSA), Operational Qualification (OQ), Performance Qualification (PQ), Update Documentation (SOP, PFMEA, Process Map) and Packaging Excellence (PEx) form
- Available for 1st shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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Last updated on Dec 10, 2024