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Manufacturing Process Engineer

Job in Philadelphia, Philadelphia County, Pennsylvania, 19113, USA
Listing for: Virtue America
Full Time position
Listed on 2026-11-06
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 45000 - 70000 USD Yearly USD 45000.00 70000.00 YEAR
Job Description & How to Apply Below

job

Title:

Manufacturing Process Engineer – Entry Level

Location: Remote

Employment Type: Full-time

Experience: 0–2 Years

Job Summary

We are seeking an Entry-Level Manufacturing Process Engineer to support manufacturing operations, process optimization, production efficiency, and continuous improvement initiatives within a pharmaceutical or life sciences environment. The ideal candidate will assist with improving manufacturing processes, troubleshooting production issues, analyzing process data, and supporting process validation activities while ensuring compliance with GMP/cGMP, FDA regulations, and quality standards
.

This opportunity is suitable for recent graduates with a background in Chemical Engineering, Mechanical Engineering, Industrial Engineering, Biomedical Engineering, or a related field.

Key Responsibilities
  • Support the development, implementation, and optimization of manufacturing processes.
  • Monitor production activities and identify opportunities to improve efficiency, productivity, and product quality.
  • Assist with process troubleshooting and investigation of manufacturing issues.
  • Collect and analyze production data, cycle times, yield, and process performance metrics.
  • Support process validation, qualification, and process improvement activities.
  • Assist with IQ/OQ/PQ documentation and process performance qualification (PPQ), as applicable.
  • Participate in root cause analysis and corrective and preventive action (CAPA) activities.
  • Prepare and maintain process flow diagrams, SOPs, work instructions, and technical reports.
  • Support equipment installation, process scale-up, and manufacturing line improvements.
  • Collaborate with Manufacturing, Quality Assurance, Quality Control, Engineering, and Validation teams.
  • Ensure manufacturing processes comply with GMP/cGMP, FDA requirements, and Good Documentation Practices.
  • Participate in Lean Manufacturing and continuous improvement initiatives.
Required Qualifications
  • Bachelor's degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, Biomedical Engineering, Biotechnology
    , or a related field.
  • 0–2 years of experience in manufacturing, process engineering, production, or pharmaceutical operations.
  • Recent graduates and candidates with relevant internships or academic projects are encouraged to apply.
  • Basic understanding of manufacturing processes, process optimization, and troubleshooting.
  • Familiarity with GMP/cGMP, SOPs, and manufacturing documentation.
  • Strong analytical, problem-solving, communication, and organizational skills.
  • Proficiency in Microsoft Excel, Word, and PowerPoint.
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