About the Role

We’re looking for a detail-oriented and process-focused Entry-Level Batch Record Reviewer to join our pharmaceutical manufacturing team. This role is ideal for someone with strong organizational skills and technical writing ability, or a junior chemical engineering background looking to build experience in a regulated industry.

Key Responsibilities

• Review completed batch production records for accuracy, completeness, and compliance with Good Manufacturing Practices (cGMP).
• Identify and document discrepancies, deviations, or incomplete information in batch records.
• Work cross-functionally with manufacturing, quality, and document control teams to ensure timely resolution of issues.
• Support efforts to streamline and improve batch documentation processes.
• Ensure proper filing and archival of reviewed records in compliance with company procedures.
• Follow standard operating procedures (SOPs) and work instructions related to batch record review.

Qualifications

• Bachelor’s degree in a technical field (e.g., Chemical Engineering, Life Sciences, Technical Writing) is preferred but not required.
• Strong attention to detail and ability to spot inconsistencies in technical documents.
• Effective written and verbal communication skills.
• Comfortable working in a fast-paced, team-oriented environment.
• Basic proficiency in Microsoft Office applications (Word, Excel, Outlook).

Bonus Skills (Not Required)

• Exposure to GMP environments or production documentation.
• Experience with batch records, SOPs, or compliance-related work.