On-Site Validation Engineer – Aseptic Fill Finish Expert

Piper Companies; Clayton (NC); On-site; USD 114,000 - 128,000; Full time

Benefits offered by this job

Sick leave if required by law

Medical, dental, vision insurance

401K

Job summary

A globally recognized biologics company is seeking a Validation Engineer for an on-site position in Clayton, NC. The role involves executing validation protocols, preparing documentation, and ensuring compliance in aseptic pharmaceutical manufacturing. Candidates should have 2–5 years of validation experience and knowledge of GMP. A competitive salary range of $114,000‑128,000/year and comprehensive benefits are included.

Qualifications

• 2–5 years of hands‑on validation experience in aseptic pharmaceutical manufacturing.
• Experience with filling isolator equipment highly preferred.
• Must be able to work on‑site five days a week.

Responsibilities

• Execute validation protocols on aseptic fill finish lines.
• Draft, review, and execute IQ/OQ/PQ protocols.
• Prepare and maintain validation documentation in TIMS.

Skills

Validation in aseptic pharmaceutical manufacturing

GMP understanding

Proficiency in TIMS

Job description

A globally recognized biologics company is seeking a Validation Engineer for an on-site position in Clayton, NC. The role involves executing validation protocols, preparing documentation, and ensuring compliance in aseptic pharmaceutical manufacturing. Candidates should have 2–5 years of validation experience and knowledge of GMP. A competitive salary range of $114,000‑128,000/year and comprehensive benefits are included.