Sr Engineer - Equipment Technical Assessments

BioPharma Consulting JAD Group

Juncos (PR)

On-site

USD 100,000 - 140,000

Full time

3 days ago
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Job summary

BioPharma Consulting JAD Group is seeking a Senior Engineer to support Drug Substance Facilities and Engineering at a biopharmaceutical site in Juncos, Puerto Rico. You will independently assess manufacturing equipment and systems, applying advanced engineering principles to optimize processes, troubleshoot, and modify systems of significant scope.

Responsibilities include preparing technical reports, evaluating equipment issues, supporting deviations and change controls, and reviewing drawings

Qualifications

  • Experience in regulated pharmaceutical or biotechnology manufacturing environments.
  • Experience with purification, fermentation, process equipment, utilities or pharmaceutical manufacturing systems.
  • Strong knowledge of cGMP and validation requirements; inspection-ready documentation.
  • Strong field presence and willingness to inspect equipment in manufacturing areas.

Responsibilities

  • Prepare, review and approve technical reports, engineering assessments, equipment evaluations and technical justifications.
  • Evaluate equipment failures, performance issues, maintenance history and operating conditions, and their potential impact on product, process, quality and qualified state.
  • Provide technical support for deviations, investigations, CAPAs, change controls, risk assessments and regulatory commitments.
  • Assess equipment design, reliability, lifecycle documentation and maintenance strategies for continued fitness for use.
  • Review engineering drawings, specifications, vendor documentation, work orders, calibration records and historical performance data.
  • Collaborate with Manufacturing, Maintenance, Automation, Validation, Quality, Process Development and vendors.
  • Develop technical solutions to complex problems and coordinate the work of engineers, consultants and vendors as needed.

Skills

Technical writing
Problem solving
Communication
Project management
Vendor management
Team collaboration

Education

Doctorate degree
Master's degree + 2 years of engineering experience
Bachelor's degree in Engineering + 4 years of engineering experience

Job description

We are seeking a Senior Engineer to support Drug Substance Facilities and Engineering at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. This role independently performs technical assessments of manufacturing equipment and systems, and applies advanced engineering principles to process optimization, troubleshooting and system modifications of significant scope and complexity.

Key Responsibilities
  • Prepare, review and approve technical reports, engineering assessments, equipment evaluations and technical justifications.
  • Evaluate equipment failures, performance issues, maintenance history and operating conditions, and their potential impact on product, process, quality and qualified state.
  • Provide technical support for deviations, investigations, CAPAs, change controls, risk assessments and regulatory commitments.
  • Assess equipment design, reliability, lifecycle documentation and maintenance strategies for continued fitness for use.
  • Review engineering drawings, specifications, vendor documentation, work orders, calibration records and historical performance data.
  • Collaborate with Manufacturing, Maintenance, Automation, Validation, Quality, Process Development and vendors.
  • Develop technical solutions to complex problems and coordinate the work of engineers, consultants and vendors as needed.
Education (one of the following)
  • Doctorate degree; OR
  • Master's degree + 2 years of engineering experience; OR
  • Bachelor's degree in Engineering + 4 years of engineering experience
Preferred Qualifications
  • Experience performing technical assessments of equipment in a regulated pharmaceutical or biotechnology manufacturing environment
  • Experience with purification, fermentation, process equipment, utilities or pharmaceutical manufacturing systems
  • Strong knowledge of cGMP and validation requirements; inspection-ready documentation
  • Strong field presence and willingness to inspect equipment in manufacturing areas
Key Skills
  • Strong technical writing, problem-solving and communication skills
  • Ability to independently manage multiple assessments and deliverables
  • Collaboration, facilitation and basic project management
  • Management of contractors and vendors
  • Contract position: approximately 12 months (through September 2027), with possible extension
  • Shift: Administrative shift
  • Days: Monday to Friday, 8 hours/day (40 hours/week)
  • On-site in Juncos, Puerto Rico
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