SonicJobs Logo
Left arrow iconBack to search

Audit Supervisor

THE RITEDOSE CORPORATION
Posted 8 days ago, valid for 24 days
Location

Columbia, SC 29206, US

Salary

$65,000 - $75,000 per year

Contract type

Full Time

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • The Ritedose Corporation in Columbia, SC is seeking an Audit Supervisor with a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related field.
  • The position requires 3-5 years of experience in the pharmaceutical manufacturing industry with a focus on quality control.
  • The salary range for this role is between $65,000.00 and $75,000.00 per year.
  • Key responsibilities include overseeing internal audits, supplier quality management, and ensuring compliance with regulations.
  • Candidates should also have knowledge of cGMP/21CFR regulations and experience supporting FDA or regulatory audits.

Job DetailsJob Location: The Ritedose Corporation - Columbia, SC 29203Education Level: 4 Year DegreeSalary Range: $65,000.00 - $75,000.00 Salary/yearJob Category: QA - Quality ControlJob Description: The Audit Supervisor supports the internal audit program, supplier quality management activities and coordination/execution of customer and regulatory audits. This role is responsible for overseeing day-to-day audit activities, ensuring compliance, and guiding audit team members.   Responsibilities: Support execution of internal audits according to the Internal Audit Master Plan Monitor and follow up on corrective action implementation related to audit findings Assist in the oversight of the supplier quality management process Conduct supplier audits, including on-site inspections when required Maintain records of audits performed and assist in scheduling repeat audits Support coordination and tracking supplier quality alerts Participate in regulatory and customer audits and assist with audit readiness activities Perform trending of audit findings and report opportunities for improvement to management Maintain current knowledge of applicable regulations and guidance documents Provide guidance and day-to-day direction to audit team members QualificationsQualifications: Bachelors’ degree in Pharmacy, Chemistry, Biology or related field 3-5 years’ experience in the pharmaceutical manufacturing industry with a quality background Working knowledge of cGMP/ 21CFR regulations ASQ Certified Quality Auditor (CQA), or ability to obtain certification within 12 months of hire Experience supporting FDA or regulatory audits Proficient with word processing and database software




Learn more about this Employer on their Career Site

Apply now in a few quick clicks

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.