Senior Process Engineer – Pharma/Biotech, Onsite

Cis-International-LLC

Juncos (PR)

On-site

USD 120,000 - 180,000

Full time

5 days ago
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Job summary

Cis-International-LLC in Juncos, PR seeks a senior design/process engineer to direct and implement major system modifications in pharma/medical device settings. You will apply advanced engineering principles to solve operational challenges and lead cross-functional teams to deliver complex projects.

Responsibilities include developing new engineering techniques, coordinating with manufacturing, utilities, QA, and validation, and creating policies and procedures that affect multiple units.

Qualifications

  • Experience in medical device or pharma environments.
  • Bilingual English/Spanish.
  • Knowledge of packaging equipment.
  • Experience with validation protocols.
  • Experience leading engineers and coordinating vendors.
  • Ability to work on on-site, multi-disciplinary projects.

Responsibilities

  • Develop technical solutions to complex problems requiring ingenuity.
  • Work with multiple departments to define requirements for major system modifications.
  • Coordinate project schedules, budgets and quality constraints.
  • Lead teams of engineers and technicians.
  • Develop engineering policies and procedures affecting multiple units.
  • Validate and document processes per GLP/GMP.

Skills

Pharma processes
Validation processes
GLP GMP knowledge
Lab equipment operation
Regulated documentation
Engineering principles
Problem solving
Project management
English Spanish bilingual

Education

Doctorate or Masters
Bachelors in Engineering

Job description

Cis-International-LLC in Juncos, PR seeks a senior design/process engineer to direct and implement major system modifications in pharma/medical device settings. You will apply advanced engineering principles to solve operational challenges and lead cross-functional teams to deliver complex projects.

Responsibilities include developing new engineering techniques, coordinating with manufacturing, utilities, QA, and validation, and creating policies and procedures that affect multiple units.

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