Commissioning Qualification Validation Engineer Position Available In Durham, North Carolina

Tallo's Job Summary: The Commissioning Qualification Validation Engineer (CQV) position in Raritan, NJ, offered by an innovative pharmaceutical manufacturer, involves leading commissioning, qualification, and validation activities for laboratory equipment and systems to ensure compliance with GMP standards. Candidates need a Bachelor's degree in engineering or Life Sciences, 3-5 years of CQV experience, and a strong understanding of regulatory guidelines. The salary ranges from $110,000 to $140,000 with comprehensive benefits.

Company:
Zachary Piper Solutions
Salary:
JobFull-timeOnsite

Job Description

Commissioning Qualification Validation Engineer
Piper Companies is currently looking for an experienced Commissioning Qualification Validation Engineer (CQV) in Raritan, New Jersey (NJ) to work for an innovative and growing pharmaceutical manufacturer.
Responsibilities for the Commissioning Qualification Validation Engineer (CQV)
include:

Commissioning:

Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended.

Qualification:

Develop, execute, and document qualification protocols (IQ/OQ/PQ) for laboratory equipment, analytical instruments, and systems to ensure compliance with GMP and regulatory standards.

Validation:

Lead validation efforts for laboratory processes, methods, and equipment, ensuring the reliability, consistency, and reproducibility of results. Support the validation lifecycle of laboratory systems, from planning through execution and reporting.

Documentation:

Prepare, review, and approve CQV documentation, including protocols, reports, and deviation investigations, ensuring compliance with all internal and external quality requirements.
Qualifications for the Commissioning Qualification Validation Engineer (CQV)
include: Bachelor’s degree in engineering, Life Sciences, or a related field (e.g., Biomedical, Chemical, Mechanical Engineering, etc.). Minimum of 3-5 years of experience in Commissioning, Qualification, and Validation (CQV) within a GMP regulated environment, preferably in the biotechnology, pharmaceutical, or cell therapy industry. Strong understanding of GMP, FDA, EMA, and ICH guidelines related to pharmaceutical/biotech operations.
Compensation for the Commissioning Qualification Validation Engineer (CQV)
include: Salary Range 110,000 – $140,000 dependent upon experience. Comprehensive benefits package
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:

140734

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