QC Document Review - Pharma

• Understand common data integrity violations in the Quality Control Laboratory. This knowledge is critical to be successful in this role.
• Stay current on publications released by USP EU FDA and other pertinent organizations including publications associated with ISO 17025:2017 accreditation to ensure the Quality Control Department complies in the areas of analytical applications release specifications and documentation practices.
• Review Quality Control Department inhouse generated data reports Contract Laboratory reports and Quality Control Certificates of Analysts using electronic signature in a timely manner. This may also include data packets associated with Method Validation or Method Development and review Certificates of Analysis produced after data review.
• Assist with the review and writeup of OutofSpecification and OutofTrend investigations generated in the QC laboratory this includes Contract Laboratory investigations. Ensure the responsible personnel/contract lab initiate investigations in a timely manner and ensure the review of data is performed in a timely manner for all stages of the investigation.
• Assist with the initiation of investigation discussions with laboratory personnel and be involved with all diagnostic discussions occurring before investigation retesting begins.
• Will receive training on test methods pertinent and prior to reviewing data reports.
• Review data associated with Special Request samples.

Minimum Requirements:

Must have 1 3 years working in a cGMP environment. Effective interpersonal selfmotivation skills and the ability to interact with all levels of personnel are required. Communicate effectively with other departments within the organization and function within a team environment. Knowledge of data integrity violations in the Quality Control Laboratory is preferred.

Education and Experience:

A Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) degree in a sciencerelated field such as Chemistry Biochemistry or Biology.

• ABachelor of Science (B.S.) orBachelor of Arts (B.A.) degree
• 1 3 years working in a cGMP environment. Effective interpersonal selfmotivation skills and the ability to interact with all levels of personnel are required. Communicate effectively with other departments within the organization and function within a team environment. Knowledge of data integrity violations in the Quality Control Laboratory is preferred.

Use your experience to make a difference! Excellent benefits.