Description of the job
Job Title: Cleaning Validation Engineer (CIP & Execution Specialist)
Location: RTP, NC
Shift: Primarily Day Shift; potential for Night Shift
Job Summary:
Seeking an experienced Cleaning Validation SME to lead CIP processes, execute cleaning validation protocols, and manage large equipment cleaning in a biopharmaceutical environment. Expertise in MACO calculations, method validation, and compliance with regulatory standards is essential.
Key Responsibilities:
- Lead CIP cycle development and cleaning validation for bioreactors, tanks, and ancillary systems.
- Perform MACO assessments and execute validation protocols (IOQ/PQ).
- Collaborate with cross-functional teams on cleaning strategies and troubleshooting.
- Conduct method validation (e.g., swab and rinse sampling).
- Ensure cGMP compliance and support regulatory audits.
Qualifications:
- Bachelor's degree in Engineering, Biotechnology, or Chemistry.
- 5+ years of cleaning validation experience with CIP and large-scale equipment.
- Expertise in MACO calculations and validation documentation.
- Knowledge of biopharmaceutical manufacturing and regulatory standards.
- Strong problem-solving and technical writing skills.
Preferred:
- Experience with automated cleaning systems and process validation.
- Familiarity with cross-contamination control strategies.