Senior Manufacturing Engineer

hace 2 meses


Juncos, Puerto Rico Quality Consulting Group A tiempo completo

Job Title: Senior Manufacturing Engineer

About the Job:
At Quality Consulting Group, we are seeking a highly motivated and experienced Senior Manufacturing Engineer to join our team. As a Senior Manufacturing Engineer, you will be responsible for providing and/or directing the characterization of process optimization strategies and/or troubleshooting of operational issues in the manufacturing environment.

Responsibilities:

  • Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the manufacturing environment.
  • Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects.
  • Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.
  • Complete complex or novel assignments requiring development of new and/or improved engineering techniques and procedures.
  • Develop engineering policies and procedures that affect multiple organizational units.
  • Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians on an ongoing basis as well as on a project basis.
  • Employ advanced engineering techniques and/or modifications of advanced techniques within area of engineering expertise.
  • Apply knowledge of engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields.
  • Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining methodologies in that area.
  • Application of mature engineering knowledge in planning and conducting projects.

Qualifications:
  • Bachelor Degree in Engineering (Mechanical or Chemical Engineering)
  • Experience Writing technical documents
  • Knowledge of Filling and Process Validation
  • Five (5) years of Previous experience in Engineering
  • Knowledge of pharmaceutical/biotech processes
  • Familiarity with documentation in a highly regulated environment
  • Ability to operate specialized laboratory equipment and computers as appropriate
  • Ability to interpret and apply GLPs and GMPs.
  • Ability to apply engineering science to production.

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