A Master's degree, or a Bachelor's degree in Engineering plus two years of engineering experience.
Bilingual English and Spanish communication.
Experience in statistical analysis.
Experience in biotech or pharmaceutical companies.
Experience in drug substance manufacturing or technical support.
Familiarity with validation processes and validation protocol execution and writing.
Ability to interpret and apply Good Manufacturing Practices and Good Laboratory Practices, and document work in a highly regulated environment.
Ability to perform analytical problem solving and applied engineering.
Ability to write technical reports and deliver basic technical presentations.
Personal organization and ability to manage change.
Computer literacy.
Responsibilities
Provide solutions to technical problems of moderate scope and complexity using standard engineering techniques and procedures.
Act as a technical expert for equipment and systems during troubleshooting; support daily operations to meet schedules and resolve complex problems.
Audit the operational performance and regulatory compliance of equipment and systems.
Work with Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance, and Validation to develop requirements and recommendations for system modifications.
Support design, engineering, and construction projects within schedule and budget; obtain and critique equipment quotes and prepare cost estimates and schedules.
Organize, analyze, and present results for operational issues and engineering projects.
Desired Qualifications
Chemical Engineering background.
Engineer - Commercial Engineering Support
BioPharma Consulting JAD Group · Juncos, Puerto Rico · Contract · Posted 2026-10-19
Workplace: on_site
Description
We are seeking an Engineer to provide engineering support to commercial operations at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. Under general supervision, this role characterizes process optimization strategies, troubleshoots operational issues and applies engineering principles to system modifications, experiments and capital projects.
Key Responsibilities
Provide solutions to technical problems of moderate scope and complexity using standard engineering techniques and procedures.
Act as technical expert for equipment and systems during troubleshooting; support daily operations to meet schedules and resolve complex problems.
Audit the operational performance and regulatory compliance of equipment and systems.
Work with Manufacturing, Maintenance, Process Development, Utilities, Facilities, QA and Validation to develop requirements and recommendations for system modifications.
Support design, engineering and construction projects within schedule and budget; obtain and critique equipment quotes and prepare cost estimates and schedules.
Organize, analyze and present results for operational issues and engineering projects.
Requirements
Education
Master's degree; OR Bachelor's degree in Engineering + 2 years of engineering experience
Preferred background: Chemical Engineering
Preferred Qualifications
Statistical analysis experience
Experience in biotech/pharmaceutical companies
Drug substance manufacturing or technical support experience
Familiarity with validation processes and validation protocol execution and writing
Ability to interpret and apply GMPs and GLPs; documentation in a highly regulated environment
Key Skills
Analytical problem solving and applied engineering
Technical report writing and basic technical presentations
Personal organization and managing change
Computer literacy; bilingual English/Spanish communication
Benefits
Contract position: approximately 24 months (November 2026 – November 2028), with possible extension
Shift: 1st shift / Administrative shift
Days: Monday to Friday, 8 hours/day (40 hours/week)