The Role
Oversee and execute internal, supplier, customer, and regulatory audits for pharmaceutical manufacturing. Manage corrective actions, supplier quality processes, audit records, trending of findings, and provide day-to-day guidance to the audit team to ensure cGMP compliance and audit readiness.
Summary Generated by Built In
Job 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
Qualifications:
- 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
Skills Required
- Bachelor's 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/21 CFR 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
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The Company
What We Do
The Ritedose Corporation is a leading pharmaceutical contract development and manufacturing organization (CDMO) specializing in sterile Blow-Fill-Seal (BFS) technology for branded and generic medications.








