
location_onGulf, 00666, United States
Quality Consulting Group is a leader in the pharmaceutical, biotech, medical devices, and manufacturing industries. We are dedicated to delivering world-class solutions across our operations in Puerto Rico and the USA.
We are seeking a talented, highly motivated, and enthusiastic professional to join our team. In this role, you will contribute to a dynamic environment where you independently direct process optimization strategies and troubleshoot operational issues within manufacturing, pilot plant, or capital project settings. You will serve as a peer-recognized engineering technology specialist, determining methodologies and applying advanced engineering techniques to complex system and facility modifications.
This position requires close collaboration with research, manufacturing, process development, utilities, facilities, quality assurance, and validation departments. You will work alongside project managers to ensure design and engineering projects are completed within schedule, budget, and quality constraints, while also supervising and reviewing the work of engineers, associates, and technicians.
Please note that this role operates on an administrative shift. However, flexibility is essential, as support may be required for non-standard shifts based on manufacturing line production demands.
Quality Consulting Group, LLC is an equal opportunity employer. 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.
Work model: On-site
Gulf, 00666, United States
Experience with C&Q process, Validation and Packaging equipment.
Skills: C&Q Process, Validation, Packaging Equipment.
Education: Bachelor's degree in Engineering Required.
Quality Consulting Group, LLC operates as a specialized consulting firm based in San Juan, PR, focusing on the outsourcing and offshoring consulting industry. The organization serves the manufacturing sector, specifically within the pharmaceutical, biotechnology, food, and medical device markets. Since its inception in 2002, the firm has delivered services across regulatory compliance, quality operations, validation, manufacturing, training, and technical support.
The company assists clients in implementing current standards, including Validation Guidance, ICH Guidelines, and Process Excellence and Risk Management tools. Its expertise covers business, operational, quality, regulatory, and manufacturing strategies, alongside organizational structures and management controls. The team provides guidance on manufacturing and quality systems methodologies, compliance programs, accuracy reviews, and regulatory matters involving the FDA, EMEA, and other global authorities. This approach supports organizations in optimizing their operational frameworks while maintaining adherence to strict industry regulations.
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Experience
4+ yrs (Senior)
Education
Bachelor's degree in Engineering Required
Job Type
Full-Time
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