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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, analyses and presents interpretation of results for operational issues or engineering projects of minor scope and complexity.

+ Provides solutions to a variety of technical problems of moderate scope and complexity.

+ Evaluate, select and apply standard engineering techniques and procedures.

+ Assistance given for unusual problems.

+ Perform assignments that have clear and specific objectives and require investigation of limited number of variables.

+ Function as a technical expert to equipment or systems regarding troubleshooting operations.

+ Frequently become actively involved in daily operations when required to meet schedules or to resolve complex problems.

+ 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.

+ Work under the direct supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints.

+ Work with consultants, architects and engineering firms on development of standard design documents.

+ Obtain and critique quotes for equipment modifications or installations.

+ Generate rudimentary project cost estimates and schedules.

Qualifications:

+ Bachelor’s degree in Engineering, preferably in Chemical or Industrial Engineering, Biotechnology, or a related technical discipline.

+ 2 years of Engineering experience.

+ Hands-on experience in process engineering, manufacturing support, or production systems within a regulated environment (biotech, pharmaceutical, or similar).

+ Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean Six Sigma, Kaizen, root cause analysis).

+ Demonstrated ability to troubleshoot manufacturing issues, implement corrective/preventive actions (CAPA), and drive process optimization.

+ Proven experience working with operations, quality, and maintenance teams to deliver results in a fast-paced environment.

+ Understanding of cGMP, compliance, and documentation practices for regulated industries.

+ Strong communication, adaptability to change.

+ 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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