GMP Quality Technician – Batch Records

PeopleShare by PROMAN; Moorestown Township (NJ); On-site; USD 25,000 - 36,000; Full time

Job summary

PeopleShare is seeking a detail-oriented Quality Technician - Batch Records to join a growing pharmaceutical organization in Moorestown, NJ. This position plays a critical role in ensuring compliance with GMP (Good Manufacturing Practices) and supporting the preparation of clinical supplies through the review, approval, and auditing of batch record documentation.

If you have experience working in a GMP-regulated environment, strong documentation skills, and an exceptional eye for detail, we want

Qualifications

• Experience in GMP-regulated environments or pharmaceutical manufacturing is preferred.
• Strong documentation and record-keeping abilities.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office Suite (Excel, Word, Outlook, Access).
• Ability to work in a fast-paced, detail-oriented setting and manage multiple priorities.

Responsibilities

• Maintain work areas in GMP-compliant condition.
• Review and approve batch-record related documentation (unexecuted batch records, packaging samples, material specs, label batch records, change controls).
• Verify client approval of reviewed documentation.
• Audit and release Executed Batch Records (EBRs).
• Collaborate with Packaging and Quality Control teams to resolve discrepancies.
• Provide guidance to packaging staff to improve documentation quality and compliance.
• Maintain document control procedures and records; assist with SOPs and data collection forms.
• Enter and verify data in the Inventory Control System (ICS) and create/revise controlled documents in ZenQMS.
• Support client and regulatory audits as required.

Skills

Attention to detail

Communication skills

Interpersonal skills

Multitasking

Analytical skills

Education

Bachelor's degree or equivalent combination of education and experience

Tools

Microsoft Office

Job description

PeopleShare is seeking a detail-oriented Quality Technician - Batch Records to join a growing pharmaceutical organization in Moorestown, NJ. This position plays a critical role in ensuring compliance with GMP (Good Manufacturing Practices) and supporting the preparation of clinical supplies through the review, approval, and auditing of batch record documentation.

If you have experience working in a GMP-regulated environment, strong documentation skills, and an exceptional eye for detail, we want