Inteldot has over 14 years of experience in the life sciences industry, with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.

Job Description

Under general supervision, provide technical support to equipment related problems and perform troubleshooting. Actively involved in daily operations when required to meet schedules or to resolve complex problems.

Non-Standard Shift

Requirements:

  • Experience in drug substance/API operations.
  • Experience in GMP-related field (manufacturing operations, engineering operations) (preferred)
  • Ability to resolve equipment-related problems by; using technical skills to analyze conditions.
  • Understanding variables that impact the process.
  • Proposing and implementing solutions.
  • Understanding of control systems (input, output, control). Programmable Logic Controllers (PLC).
  • Experience in equipment start-up and troubleshooting.
  • Strong knowledge of manufacturing equipment, failure modes, and troubleshooting for: valves, pumps, utilities systems
  • Excellent self-learning skills and ability to leverage technology effectively.

  • Functions:

    • Provide solutions to technical problems of moderate scope and complexity.
    • Evaluate, select, and apply standard engineering techniques and procedures under general supervision.
    • Routinely audit operational performance and regulatory compliance of moderate-to-complex equipment or systems.
    • Collaborate with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance, and validation teams to develop requirements and system modification recommendations.
    • Collaborate with consultants, architects, and engineering firms to develop standard design documents.

    Education:

    Bachelor’s degree in engineering & 2 years of engineering experience (Chemical Engineering, Mechanical Engineering, and Electrical engineering fields are preferable)