Cleaning Validation Engineer (Pharma) Position Available In Wake, North Carolina

Tallo's Job Summary: The Cleaning Validation Engineer position at Piper Companies involves developing and executing cleaning validation protocols, conducting risk assessments, collaborating with cross-functional teams, performing studies, and maintaining detailed documentation. The role requires a Bachelor's degree, 5+ years of experience in biopharmaceutical cleaning validation, strong GMP knowledge, and proficiency in statistical analysis. Compensation ranges from $60-$80/hr with benefits included.

Company:
Zachary Piper Solutions
Salary:
$145600
JobFull-timeOnsite

Job Description

Cleaning Validation Engineer (Pharma)
Piper Companies is looking for a Cleaning Validation Engineer that will play a critical role in the development, implementation, and maintenance of cleaning validation processes for a brand new manufacturing facility. This position requires a thorough understanding of cleaning validation principles, regulatory requirements, and industry best practices. The successful candidate will ensure that all cleaning procedures are validated and compliant with GMP standards.
This is an on-site position in the greater Raleigh, NC area.
Responsibilities of the Cleaning Validation Engineer
: Develop and execute cleaning validation protocols and reports for new equipment and facilities. Perform risk assessments to identify potential contamination sources and establish appropriate cleaning procedures. Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to ensure cleaning validation activities are integrated into the overall project plan. Conduct cleaning validation studies, including sampling, testing, and data analysis. Investigate and resolve deviations and discrepancies related to cleaning validation. Maintain accurate and detailed documentation of all cleaning validation activities. Train personnel on cleaning validation procedures and best practices. Stay current with industry trends, regulatory changes, and advancements in cleaning validation technologies. Qualifications of the Cleaning Validation Engineer
: Bachelor’s degree in Engineering, Microbiology, Chemistry, or a related field. Minimum of 5+ years of experience in cleaning validation within the biopharmaceutical industry (more than 5 years preferred). Strong knowledge of GMP regulations and cleaning validation guidelines. Experience with greenfield projects and new facility build-outs is highly desirable. Excellent analytical, problem-solving, and communication skills. Ability to work independently and as part of a team in a fast-paced environment. Proficiency in statistical analysis and data interpretation. Compensation of the

Cleaning Validation Engineer:
Pay Range:

$60-$80/hr depending on experience

Benefits:

Health, dental, vision, PTO, and sick leave as required by law. Also, you’ll be part of a team working on what will be the largest CDMO of its kind.
This job opens for applications on 5/22/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
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Dice Id:

10430981

Position Id:

142312

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