Night QA Specialist, cGMP & PET Manufacturing

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

Benefits offered by this job

Medical, dental, vision

401k

PTO

HSA

Job summary

Cardinal Health in Fort Lauderdale, FL is seeking a Sr. Specialist, Quality Assurance for an onsite night shift. The role focuses on cGMP documentation review, product release, and collaboration with operations to uphold quality systems.

The position requires a science background with 2+ years in QA/cGMP and strong written/verbal English skills, with potential travel up to 25% and a shift from 1:00 am to 9:30 am. Internal growth and comprehensive benefits are offered.

Qualifications

• Bachelor's degree in related field (science) preferred, or equivalent work experience.
• 2+ years of experience in related science field preferred
• 1-2 years of experience in Quality Assurance and/or cGMP regulated 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

• Handles cGMP documentation review related to product release, facilities and equipment, material controls, laboratory controls, packaging and labeling, and production & process controls.
• Establishes and reports metrics related products and processes as deemed necessary by the Regional Quality Manager (RQM).
• Ensures the site manufactures products to meet the requirements of 21 CFR 212 (cGMP).
• Handles and ensures quality of documentation (control, retention, and archival) to support cGMP activities.
• Engages and collaborates with operations department to drive quality system and cGMP requirements.
• Performs product release activities per cGMP requirements.
• Reports quality system issues to the RQM and others as necessary.

Skills

Quality Assurance

cGMP

English communication

Education

Bachelor's degree in science

Job description

Cardinal Health in Fort Lauderdale, FL is seeking a Sr. Specialist, Quality Assurance for an onsite night shift. The role focuses on cGMP documentation review, product release, and collaboration with operations to uphold quality systems.

The position requires a science background with 2+ years in QA/cGMP and strong written/verbal English skills, with potential travel up to 25% and a shift from 1:00 am to 9:30 am. Internal growth and comprehensive benefits are offered.