Pharma QA Specialist: Doc Release & Compliance

Dexian; Myerstown (PA); On-site; USD 41,328 - 48,216; Part time

Job summary

A leading staffing provider is seeking a Quality Assurance professional to perform document reviews and audits in a pharmaceutical setting. Responsibilities include ensuring compliance with GMP standards, coordinating with QA teams, and maintaining quality databases. Candidates should have at least 5 years of experience in a relevant role, possess strong interpersonal skills, and be able to lift up to 50 pounds. This role offers a contract position with competitive pay.

Qualifications

• 5+ years in a cGMP document review/auditing role.
• Strong PC skills, preferably with Microsoft software.
• Ability to physically lift up to 50 pounds.

Responsibilities

• Audit documentation for compliance with GMP.
• Coordinate with QA and contractors for timely work.
• Prepare and maintain essential QA databases.

Skills

Document review/auditing

SAP

Microsoft applications

Interpersonal skills

Communication skills

Mathematical calculation

Education

High School degree or GED

Tools

SAP

MES

Job description

A leading staffing provider is seeking a Quality Assurance professional to perform document reviews and audits in a pharmaceutical setting. Responsibilities include ensuring compliance with GMP standards, coordinating with QA teams, and maintaining quality databases. Candidates should have at least 5 years of experience in a relevant role, possess strong interpersonal skills, and be able to lift up to 50 pounds. This role offers a contract position with competitive pay.