CSV Quality Assurance Analyst II (Onsite)

Charles River Laboratories, Inc.; Pennsylvania, United States, Northern America, Americas; Híbrido; USD 90.000 - 100.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Bonus incentives

401K

Paid time off

Stock purchase program

Health coverage

Wellbeing support programs

Work life balance

Descripción de la vacante

Charles River Laboratories, Inc. is seeking a Quality Assurance CSV Specialist II for an onsite role in Wayne, PA. The position focuses on QA monitoring of regulated computer systems, ensuring regulatory compliance and supporting validation deliverables.

Ideal candidates have a scientific background and 2–4 years in pharma/biotech/IT with CSV knowledge, plus auditing experience. Strong communication across departments is essential.

Formación

• Bachelor's degree in a scientific discipline and/or computer-related field.
• 2–4 years related experience in pharma/biotech/IT with knowledge of computer validation.
• 1–2 years auditing or quality assurance preferred.
• Equivalent combination of education and experience accepted.

Responsabilidades

• Provide QA monitoring and audits of regulated computer systems to assure compliance.
• Communicate identified compliance and quality risks to supervisor.
• Develop and review validation deliverables and support continuous improvement.
• Assist in periodic assessments of IT regulated activities.
• Prepare audit reports and coordinate responses to deficiencies before use.

Conocimientos

QA monitoring

Auditing

Regulatory compliance

Computer systems validation

Documentation

Communication

Educación

Bachelor's degree in a scientific discipline or related field

Descripción del empleo

Charles River Laboratories, Inc. is seeking a Quality Assurance CSV Specialist II for an onsite role in Wayne, PA. The position focuses on QA monitoring of regulated computer systems, ensuring regulatory compliance and supporting validation deliverables.

Ideal candidates have a scientific background and 2–4 years in pharma/biotech/IT with CSV knowledge, plus auditing experience. Strong communication across departments is essential.