Aseptic Validation Engineer - PPQ & Process

Sterling Engineering; Greenville (NC); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Paid Time Off

Paid Holidays

Medical plans (3)

Dental & Vision plans

401(k) with match

ESOP

Job summary

Sterling Engineering is seeking a qualified Validation or Process Engineer for an onsite, long-term contract-to-hire role in Greenville, NC. The ideal candidate will have 5+ years of experience in aseptic processing, media fills, IQ/OQ/PQ, and sterile manufacturing within pharmaceutical settings.

You will perform hands-on process validation, PPQ, CPV, qualification, investigations, and GMP documentation. A Bachelor's degree in Engineering or a related technical field is required.

Qualifications

• Bachelor's degree in Engineering or a related technical field is required.
• Minimum 5 years of experience in aseptic processing, media fills, IQ/OQ/PQ, commercial manufacturing or regulatory inspections.
• Hands-on experience with process validation, PPQ, CPV, qualification, validation protocols, investigations and GMP documentation.
• Experience in sterile/aseptic pharmaceutical manufacturing.

Responsibilities

• Hands-on experience with process validation, PPQ, CPV, qualification, validation protocols, investigations and GMP documentation.

Skills

Aseptic processing

Media fills

IQ/OQ/PQ

Sterile manufacturing

Process validation

GMP documentation

Education

Bachelor's degree in Engineering or a related technical field

Job description

Sterling Engineering is seeking a qualified Validation or Process Engineer for an onsite, long-term contract-to-hire role in Greenville, NC. The ideal candidate will have 5+ years of experience in aseptic processing, media fills, IQ/OQ/PQ, and sterile manufacturing within pharmaceutical settings.

You will perform hands-on process validation, PPQ, CPV, qualification, investigations, and GMP documentation. A Bachelor's degree in Engineering or a related technical field is required.