JT255-PROJECT ENGINEER
Juncos, Puerto Rico
Contracted
Biopharmaceutical
Experienced
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.
We are seeking a Project Engineer to lead capital projects at a biotechnology manufacturing facility. This role involves managing the full project lifecycle—from requirements definition through implementation and close-out—ensuring projects are delivered on time, within scope, and in compliance with technical and quality standards.
Responsibilities:
Qualifications:
We are seeking a Project Engineer to lead capital projects at a biotechnology manufacturing facility. This role involves managing the full project lifecycle—from requirements definition through implementation and close-out—ensuring projects are delivered on time, within scope, and in compliance with technical and quality standards.
Responsibilities:
- Collaborate with the Manufacturing department to develop User Requirement Specifications (URS) for capital projects.
- Develop the project schedule, including installation and qualification (C&Q) activities.
- Work directly with construction and commissioning/qualification contractors to ensure delivery of project deliverables.
- Manage the implementation and close-out of projects.
- Communicate and report project status to site management.
- Monitor and assess the physical progress of engineers and contractors.
- Address claims related to progress and delays from contractors.
- Review and approve change orders and expense reports submitted by engineers.
- Prepare monthly project status reports for site senior management.
- Develop and track project schedules.
Qualifications:
- Bachelor’s degree in engineering.
- 2 years of Engineering experience.
- Experience with Process & Industrial equipment in the Pharmaceutical or Biotech industry.
- Experience in change control.
- Strong technical experience working on small projects supporting industrial process equipment and biotechnology manufacturing facilities including C&Q & start up activities for Manufacturing facilities.
- Familiarity with validation processes.
- Familiarity with documentation in a highly regulated environment.
- Ability to interpret and apply GLPs and GMPs.
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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