Engineer
BioPharma Consulting JAD Group Ver todas las vacantes
- Juncos, PR
- Autónomo
- Tiempo completo
- Provide solutions to technical problems of moderate scope and complexity
- Evaluate, select, and apply standard engineering techniques and procedures
- Execute assignments with defined objectives requiring analysis of limited variables
- Initiate and complete routine technical and engineering tasks
- Organize, analyze, and present data to support decision-making and improvements
- Serve as a technical resource for troubleshooting equipment and system issues
- Support daily manufacturing operations to meet production schedules and resolve issues
- Audit operational performance and ensure regulatory compliance of equipment and systems
- Collaborate cross-functionally with Manufacturing, Maintenance, Quality, Validation, Facilities, and Process Development teams
- Develop recommendations and requirements for system improvements and modifications
- Support project managers in design, engineering, and execution of capital projects
- Assist in completing projects within scope, schedule, and budget constraints
- Collaborate with external consultants, architects, and engineering firms
- Review and evaluate vendor quotes for equipment and system modifications
- Develop basic project cost estimates and timelines
- Analytical problem-solving and troubleshooting
- Applied engineering and technical decision-making
- Basic technical report writing and documentation
- Effective verbal and written communication
- Validation protocol execution and documentation
- Organizational and time management skills
- Adaptability and change management
- Technical presentations and cross-functional collaboration
- Equipment-specific technical knowledge
- Computer literacy (e.g., MS Office, data analysis tools)
- Master's degree in Engineering, OR
- Bachelor's degree in Engineering + 2 years of relevant experience
- Knowledge of pharmaceutical or biotechnology manufacturing processes
- Familiarity with validation processes (IQ/OQ/PQ)
- Experience working in a highly regulated environment (GMP/GLP)
- Ability to operate laboratory equipment and computerized systems
- Understanding of documentation practices in regulated industries
- Ability to apply engineering principles to production environments
- Administrative Shift
- 1-year contract