Process Engineer: GMP, Process Optimization & Capital Projects

ProQuality Network

Juncos (PR)

On-site

USD 55,000 - 83,000

Part time

3 days ago
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Job summary

ProQuality Network is seeking an Engineer to support process characterization, optimization, troubleshooting, and capital projects at their Juncos, PR site. The role involves applying engineering principles to design and implement system modifications, analyzing results, and presenting findings to cross-functional teams.

The ideal candidate has a Master’s or Bachelor’s in Engineering with 2+ years in GMP-regulated environments (pharma/biotech).

Qualifications

  • Master’s degree in Engineering, or a Bachelor’s with 2+ years of engineering experience.
  • Experience in GMP-regulated environments (pharma/medical device/biotech).
  • Familiarity with validation, packaging equipment, and process characterization.
  • Ability to apply engineering principles to production environments.
  • Strong analytical and problem-solving skills.

Responsibilities

  • Characterize processes and optimize production to reduce variability.
  • Troubleshoot operations and support capital projects.
  • Prepare technical reports and present findings.
  • Validate protocols and support DOE studies.
  • Collaborate with QA, Validation, Facilities and Manufacturing teams.

Skills

Analytical & problem-solving
Technical presentations
Statistical analysis & DOE
Documentation skills
Time management
Cross-functional collaboration

Education

Master’s degree in Engineering
Bachelor’s degree in Engineering + 2+ yrs experience

Tools

Specialized laboratory equipment
Computer systems

Job description

ProQuality Network is seeking an Engineer to support process characterization, optimization, troubleshooting, and capital projects at their Juncos, PR site. The role involves applying engineering principles to design and implement system modifications, analyzing results, and presenting findings to cross-functional teams.

The ideal candidate has a Master’s or Bachelor’s in Engineering with 2+ years in GMP-regulated environments (pharma/biotech).

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