Cleaning Validation Engineer

Accentuate Staffing; Morrisville (NC); On-site; USD 80,000 - 100,000; Full time

Job summary

Accentuate Staffing is seeking a Cleaning Validation Engineer for a pharmaceutical organization in Morrisville, NC. This role focuses on ensuring compliance through cleaning validation activities and requires strong experience in GMP environments.

The ideal candidate will lead validation processes, support regulatory inspections, and play a key role in developing SOPs and validation documents. Competitive compensation and on-site work are offered.

Qualifications

• Experience in Cleaning Validation within pharmaceutical or other regulated GMP manufacturing environments.
• Strong understanding of FDA, EU, and global cGMP regulatory requirements.
• Experience supporting regulatory inspections and audits.

Responsibilities

• Develop, maintain, and approve cleaning validation requirements.
• Own cleaning validation lifecycle activities including protocols and documentation.
• Provide leadership, mentoring, and training to site personnel.

Skills

Cleaning validation experience

GMP manufacturing exposure

Technical writing

Cross-functional communication

Education

Bachelor’s Degree in Engineering, Chemistry, Life Sciences, or related field

Job description

Accentuate Staffing is partnering with a pharmaceutical organization in the Raleigh, NC area who is hiring for a Cleaning Validation Engineer. This is a contract-to-hire or C2C opportunity offering competitive compensation while working onsite. The ideal candidate has strong cleaning validation experience, hands‑on GMP manufacturing exposure, and the ability to lead validation activities across the product lifecycle.

Responsibilities

1. Develop, maintain, and approve cleaning validation requirements ensuring compliance with regulatory and business standards
2. Own cleaning validation lifecycle activities including protocols, procedures, sampling strategies, and validation documentation
3. Review and approve cleaning procedures, inspection methods, and cleaning verification processes
4. Define testing strategies and ensure execution and documentation of cleaning validation programs
5. Support regulatory inspections, audits, and investigation activities related to cleaning validation
6. Conduct periodic reviews to ensure cleaning processes remain in a validated state
7. Revise and approve SOPs, work instructions, and cleaning‑related documentation used in manufacturing operations
8. Lead development of swab sampling strategies and testing approaches for new and existing equipment
9. Support optimization and continuous improvement initiatives for cleaning processes and compliance effectiveness
10. Provide leadership, mentoring, and training to site personnel and Cleaning Validation team members on procedures and expectations

Requirements

1. Bachelor’s Degree in Engineering, Chemistry, Life Sciences, or related field
2. Experience in Cleaning Validation within pharmaceutical or other regulated GMP manufacturing environments
3. Strong understanding of FDA, EU, and global cGMP regulatory requirements
4. Experience developing validation protocols, reports, and cleaning procedures across lifecycle phases
5. Experience supporting regulatory inspections, audits, and compliance investigations
6. Strong technical writing, documentation, and cross‑functional communication skills
7. Experience with manufacturing equipment, cleaning systems, or validation lifecycle programs preferred