JT938 - ENGINEER
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
Date Posted
02/03/2025
Views
0
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