JT953 - SR. ENGINEER

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. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.

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:

• Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects 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’s degree in Engineering (Chemical, Mechanical, Electrical, Industrial, Biomedical, or related field).

• Experience in manufacturing operations within a regulated GxP/GMP environment.

• Knowledge of manufacturing processes, equipment, packaging, and process operations.

• Experience with manufacturing systems and processes, including DME, PLM, Change Control, MMP/MPP, and Continuous Process Verification (CPV).

• Experience managing controlled documentation, GMP records, process changes, and system configuration.

• Ability to analyze manufacturing and process data, identify trends, monitor process performance, and support investigations and continuous improvement.

• Experience preparing CPV reports, presentations, and manufacturing performance reports.

• Strong proficiency in Microsoft Excel; experience with JMP, Power BI, Power Query, and SQL is a plus.

• Ability to support system configuration, testing, troubleshooting, and process improvements.

• Familiarity with Microsoft 365, Smartsheet, and automation tools is desirable.

• General Skills

• Strong analytical, engineering, and problem-solving skills.

• Excellent written and verbal communication skills.

• Fully bilingual in English and Spanish.
• Administrative Shift 

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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