JT938 - ENGINEER

Quality Consulting Group • Other US Location

Company

Quality Consulting Group

Location

Other US Location

Type

Full Time

Job Description

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:

  • Provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
  • Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects.
  • Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity
  • Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems.
  • Initiate and complete routine technical tasks.
  • Function as a technical expert to equipment or systems regarding troubleshooting operations.
  • Routinely monitor manufacturing processes for performance indicators and operations. Suggest problem resolution and provide troubleshooting guidance.
  • Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of significant complexity.
  • Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications.

Qualifications:

  • Bachelor’s degree in chemical engineering and Mechanical Engineering fields are preferable.
  • 2 years of Engineering experience
  • Working knowledge of pharmaceutical/biotech processes
  • Ability to operate specialized laboratory equipment and computers as appropriate
  • Ability to apply engineering science to production.
  • GMP experience
  • Knowledge in validation activities, preferable process validation.
  • Must be fluent in English
  • Administrative shift but must be available to work in shifts including weekend and night shift when required
Apply Now

Date Posted

02/03/2025

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