Night-Shift QA Specialist | cGMP Product Release

Cardinal Health, Inc.; Fort Lauderdale (FL); On-site; USD 69,000 - 88,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Paid time off plan

Health savings account

401k savings plan

FlexPay access to wages

FSAs

Disability coverage

Work-Life resources

Paid parental leave

Healthy lifestyle programs

Job summary

Cardinal Health, Inc. seeks a Quality Assurance professional to support cGMP manufacturing in Fort Lauderdale, FL. This onsite night-shift role requires review of cGMP documentation, product releases, and collaboration with operations to maintain quality systems.

Ideal candidates have 2+ years in a related science field and 1–2 years in QA/cGMP environments, with pharma/medical device experience a plus. Travel up to 25% may be required.

Qualifications

• Bachelor’s degree in science preferred, or equivalent work experience.
• 2+ years experience in related science field preferred.
• 1-2 years experience in Quality Assurance and/or cGMP environment highly preferred.
• Pharmaceutical or medical device experience a plus.
• Effective written and verbal English communication skills.
• ISO experience a plus.
• Ability to lift up to 30-45 lbs.

Responsibilities

• Reviews cGMP documentation for product release, facilities, materials, labs, packaging, labeling, and production controls.
• Establishes and reports metrics for products and processes as required by the RQM.
• Ensures site manufactures products to meet 21 CFR 212 (cGMP) requirements.
• Manages documentation quality including control, retention, and archival for cGMP activities.
• Collaborates with operations to drive quality system and cGMP requirements.
• Performs product release activities per cGMP requirements.
• Reports quality system issues to the RQM and others with timely escalation of discrepancies.

Skills

2+ years experience in science field

Quality Assurance / cGMP experience

English communication skills

ISO experience

Pharma/medical device exposure

Ability to lift 30-45 lbs

Education

Bachelor’s degree in science field

Job description

Cardinal Health, Inc. seeks a Quality Assurance professional to support cGMP manufacturing in Fort Lauderdale, FL. This onsite night-shift role requires review of cGMP documentation, product releases, and collaboration with operations to maintain quality systems.

Ideal candidates have 2+ years in a related science field and 1–2 years in QA/cGMP environments, with pharma/medical device experience a plus. Travel up to 25% may be required.