QA Specialist — CGMP Compliance (Night Shift)

Cardinal Health; San Antonio (TX); Sur place; USD 69 000 - 88 000; Plein temps

Avantages offerts par ce poste

Medical, dental and vision coverage

Paid time off plan

401k savings plan

myFlexPay access to wages before pay

FSAs

Short- and long-term disability

Work-Life resources

Paid parental leave

Healthy lifestyle programs

Résumé du poste

Cardinal Health PET Manufacturing Services is seeking a Quality Assurance professional to support CGMP documentation review and product release processes. You will work with operations to uphold CGMP standards and drive continuous improvement in quality systems.

The role requires a Bachelor’s degree in Science, strong English communication, and familiarity with regulated environments; pharma or medical device experience is a plus. This position is on-site with comprehensive benefits.

Qualifications

• Effective written and verbal English communication skills required.
• 0-2 years' experience in a regulated environment preferred.
• Pharmaceutical or medical device experience a plus.
• ISO experience a plus.
• Quality Assurance background preferred.

Responsabilités

• CGMP documentation review related to product release, facilities and equipment, material controls, laboratory controls, packaging and labeling, and production & process controls.
• Establish and report metrics related to products and processes as deemed necessary by the RQM.
• Ensure the site manufactures products to meet CGMP requirements.

Connaissances

English communication

Regulated environment experience

Pharma/medical device experience

ISO experience

Quality Assurance background

Formation

Bachelor's degree in Science

Description du poste

Cardinal Health PET Manufacturing Services is seeking a Quality Assurance professional to support CGMP documentation review and product release processes. You will work with operations to uphold CGMP standards and drive continuous improvement in quality systems.

The role requires a Bachelor’s degree in Science, strong English communication, and familiarity with regulated environments; pharma or medical device experience is a plus. This position is on-site with comprehensive benefits.