Job Title: Engineer (Biotechnology Industry)

Location: East Region, Puerto Rico

Positions Available: 2

Shift: 12-Hour Shifts (Non-Standard)

Duration: Approximately 6 Months

Summary

Our client is seeking two Engineers to support operations in a biotechnology manufacturing environment. Under general supervision, the selected candidates will contribute to process optimization, troubleshoot operational and equipment issues, and support design or capital project activities. The role involves applying core engineering principles to analyze systems, perform system modifications, execute experiments, and interpret results related to routine technical problems.

Key Responsibilities

General Engineering Functions

• Solve a variety of technical problems of moderate scope and complexity.
• Apply standard engineering techniques and procedures with general supervision.
• Perform assignments with clear and specific objectives involving limited variable investigation.
• Initiate and complete routine technical tasks with accuracy and efficiency.

Operations Engineering

• Act as a technical expert on equipment and systems by supporting troubleshooting and root cause analysis.
• Engage in daily operations to meet production schedules or resolve complex issues as needed.
• Audit and ensure operational performance and regulatory compliance for moderate-to-complex systems.
• Collaborate with cross-functional teams, including manufacturing, maintenance, facilities, QA, validation, utilities, and R&D, to define and recommend system modifications or improvements.

Design Engineering

• Assist project managers in delivering design, engineering, and construction projects within scope, schedule, and budget.
• Work with consultants, architects, and engineering firms to develop standard design documentation.
• Obtain and evaluate vendor quotes for equipment installations or modifications.
• Prepare basic cost estimates and project timelines.

Education and Experience Requirements

• Bachelors Degree in Engineering with a minimum of 2 years of engineering experience, or
• Masters Degree in Engineering.

Preferred Qualifications

• Chemical Engineering, Mechanical Engineering, and Electrical engineering fields are preferable.
• Hands-on experience in GMP-regulated environments (e.g., pharmaceutical or biotech manufacturing).
• Working knowledge of drug substance/API operations, control systems (input/output/control), and manufacturing equipment (e.g., pumps, valves, utility systems).
• Experience in equipment startup, troubleshooting, and working with PLC systems.
• Strong analytical and technical problem-solving skills.
• Excellent self-learning abilities and proficiency in leveraging technology for continuous improvement.
• Familiarity with validation processes and protocol execution in regulated settings.
• Comfortable interpreting and applying GLPs and GMPs.
• Proficient in using laboratory equipment and manufacturing systems.

Skills and Competencies

• Technical report writing
• Verbal and written communication
• Validation protocol writing and execution
• Basic technical presentations
• Personal organization and time management
• Change management
• Computer literacy
• Equipment-specific troubleshooting
• Analytical thinking

Apply Now

Interested candidates are encouraged to apply with an updated resume inside the job description link to be considered for this opportunity with our client: