Aseptic Fill/Finish Process Engineer – Onsite

Stark Pharma Solutions Inc

Bradley (IL)

On-site

USD 90,000 - 140,000

Full time

14 days+
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Job summary

Stark Pharma Solutions Inc. is seeking an experienced Process Engineer to support aseptic fill/finish operations at our Bradley, IL, site.

The role involves designing, implementing, starting up, and optimizing fill/finish equipment and processes to ensure sterile manufacturing readiness. Responsibilities include commissioning new lines, developing recipes, and collaborating with Validation/CQV teams during IQ/OQ/PQ.

Qualifications

  • Bachelor's degree in Engineering or related technical field.
  • 5–7+ years in pharmaceutical, biologics, or sterile manufacturing environments.
  • Experience with aseptic fill/finish manufacturing processes.
  • Hands-on experience with equipment startup, commissioning, and process optimization.
  • Familiarity with GMP manufacturing requirements and sterile processing.

Responsibilities

  • Support installation, commissioning, and startup of aseptic fill/finish lines.
  • Develop and optimize equipment recipes, operating parameters, and processes.
  • Collaborate with Validation and CQV during IQ/OQ/PQ activities.
  • Drive process improvements to improve equipment performance and product quality.
  • Troubleshoot startup and operations issues with cross-functional teams.
  • Assist with configuration, qualification, and readiness activities.
  • Train manufacturing and maintenance personnel on new systems.
  • Support timelines and compliance across projects.

Skills

Aseptic processing
Equipment startup
Process optimization
Troubleshooting
Cross-functional teamwork

Education

Bachelor's degree in Engineering

Job description

Stark Pharma Solutions Inc. is seeking an experienced Process Engineer to support aseptic fill/finish operations at our Bradley, IL, site.

The role involves designing, implementing, starting up, and optimizing fill/finish equipment and processes to ensure sterile manufacturing readiness. Responsibilities include commissioning new lines, developing recipes, and collaborating with Validation/CQV teams during IQ/OQ/PQ.

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