Engineer (Biotechnology Industry) 3371549
Job Title: Engineer (Biotechnology Industry)
Location: East Region, Puerto Rico
Positions Available: 3
Shift: 12-Hour Shifts (Non-Standard)
Duration: Approximately 6 Months
Summary
Our client is seeking two Engineers to support operations within a biotechnology manufacturing environment. Under general supervision, the selected candidates will contribute to process optimization, process and equipment troubleshooting, and the resolution of operational issues, as well as support design and capital project activities. This role requires applying core engineering principles to analyze systems, perform modifications, execute experiments, and interpret results to address routine technical challenges. Candidates will collaborate with cross-functional teams to ensure efficient, compliant, and reliable manufacturing operations.
Key Responsibilities
General Engineering Functions
- Solve a variety of technical problems of moderate scope and complexity.
- Apply standard engineering techniques and procedures under 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.
- Participate in daily operations to meet production schedules and 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
- Bachelor’s Degree in Engineering with a minimum of 2 years of engineering experience, or
- Master’s Degree in Engineering.
Preferred Qualifications
- Degree in Chemical Engineering, Mechanical Engineering, or Electrical Engineering is preferred.
- Hands-on experience in GMP-regulated environments (e.g., pharmaceutical or biotechnology manufacturing).
- Working knowledge of drug substance/API operations, control systems (input/output/control), and manufacturing equipment (e.g., pumps, valves, utility systems).
- Proficiency in using laboratory equipment and manufacturing systems.
- Experience in equipment startup, process and equipment 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.
- Ability to interpret and apply GLPs and GMPs.
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 using the job description link to be considered for this opportunity with our client.