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Record Reviewer

Express EmploymentBirmingham, AL
Job Category

Manufacturing & Production Line

Job Type

Hourly

Employment Type

Temp to Hire

Work Hours

Full-time

Compensation

$23$27per hour

Hiring Manager
Katie DaySenior Recruiter
Recruiter
Katie DaySenior Recruiter

This job was last updated on January 6, 2026 10:44 AM.

Job Title: Record Reviewer

About the Company

Our client is a pharmaceutical company in the Birmingham area that operates as an outsourcing compounding facility specializing in hormone and therapeutic wellness. They partner with healthcare providers to deliver high-quality, customized medications while maintaining strict quality, safety, and regulatory standards.

Position Overview

The Record Reviewer plays a key role in maintaining compliance and documentation accuracy within a regulated pharmaceutical manufacturing environment. This position requires a coaching-focused mindset, strong regulatory awareness, and the ability to proactively identify and resolve issues in real time. The role is hands-on and production-facing, supporting QA activities directly on the floor rather than solely through desk-based review.

Schedule & Pay

  • Monday–Friday, 8:00 AM–5:00 PM

  • On-site, full-time

  • Temp-to-perm opportunity

  • Pay range: $23–$27/hour (flexible for the right candidate; higher consideration for strong experience)

Key Responsibilities

  • Perform real-time batch record review during manufacturing operations

  • Review production and quality records for accuracy, completeness, and GMP compliance

  • Conduct GMP compliance walkthroughs in production suites

  • Identify documentation errors, trends, and gaps; proactively investigate and resolve issues

  • Coach operators and team members on SOP adherence and proper documentation practices

  • Collaborate with operators and cross-functional teams to ensure compliance throughout production

  • Provide on-the-floor QA support, not limited to desk-based record review

  • Ensure alignment with SOPs, regulatory requirements, and internal quality standards

Qualifications & Experience

  • Strong understanding of SOPs and regulated manufacturing environments

  • Working knowledge of GMPs and regulatory expectations

  • Pharmaceutical or regulated industry background preferred

  • High attention to detail with the ability to independently “hunt down” discrepancies

  • Teacher or coaching mindset focused on education and continuous improvement

  • Competent, proactive, and confident professional with a dynamic personality

  • Ability to communicate effectively across production and quality teams

Company Size

251-1000

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  2. What is the minimum hourly pay rate you're open to, and what is your target hourly rate?

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  4. Which shifts are you available to work and which do you prefer?

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  5. Have you ever performed real-time batch record reviews or quality audits on the production floor? (Yes/No)

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  6. Can you briefly describe your approach to coaching team members on SOP adherence?

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