Engineer

BioPharma Consulting JAD Group Ver todas las vacantes

  • Juncos, PR
  • Autónomo
  • Tiempo completo
  • Hace 3 días
Job Description:Under general supervision, the Process / Operations Engineer supports process optimization, troubleshooting, and engineering projects within manufacturing, operations, pilot plant, or capital project environments. This role applies fundamental engineering principles to design system modifications, execute experiments, and improve operational performance. The engineer analyzes data, interprets results, and provides solutions to technical challenges of moderate scope and complexity.Key Responsibilities
  • 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
Core Competencies
  • 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)
Requirements:Education & Experience
  • Master's degree in Engineering, OR
  • Bachelor's degree in Engineering + 2 years of relevant experience
Preferred Qualifications
  • 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
Benefits:
  • Administrative Shift
  • 1-year contract

BioPharma Consulting JAD Group

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