Amneal Pharmaceuticals logo

Batch Record Reviewer I - 1st Shift

Amneal Pharmaceuticals

Piscataway, NJJobSeen 1 day agoSeen in employer's feed 1 day ago

Most applications go out cold — see where you stand first. No sign-up to start.

Watch jobs like this.

At a glance

Compensation
No compensation found
Location
Piscataway, NJ
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The Batch Record Reviewer I reviews manufacturing documentation for completeness, accuracy, and compliance with cGMP, internal quality standards, and regulatory requirements before product release. The role identifies and escalates discrepancies, supports lot status updates and audits, and partners with Production, Quality Assurance, Compliance, and Investigation groups to support product release, data integrity, and quality initiatives.

Skills & qualifications

RequiredNice to have

Skills

Batch Record ReviewCGMP ComplianceSOP ComplianceRegulatory ComplianceData VerificationDiscrepancy ResolutionDeviation DocumentationAudit SupportProduction Room ReleaseIn-Process ChecksE-Log Book ReviewPreventive Maintenance CoordinationProduction Operations

Full job description

Description:

The Batch Record Reviewer I is responsible for the accurate and timely review of batch records to ensure compliance with cGMP, internal quality standards, and regulatory requirements. This role involves verifying data entries, calculations, and documentation for completeness and accuracy, identifying and resolving discrepancies, and ensuring that all deviations, investigations, and change controls are properly documented and addressed. The reviewer works closely with Production, Quality Assurance, and other cross-functional teams to support product release, maintain data integrity, and uphold product quality and patient safety.

Essential Functions:

  • Perform final review of manufacturing documentation for completeness and compliance with cGMP, SOPs, and regulatory requirements before release.

  • Deliver requested lot status updates to support production and quality activities.

  • Ensure that deviations, discrepancies, and non-conformances are properly documented and escalated for investigation.

  • Document and report identified documentation errors to management, ensuring proper tracking for trend analysis and use in training and continuous improvement initiatives

  • Support compliance and quality initiatives by partnering with QA–Manufacturing, Compliance, and Investigation groups during real-time reviews, and providing record retrieval and filing assistance across departments.

  • Provide support during internal/external audits, as requested.

Additional Responsibilities:

  • Perform additional duties as requested.

  • Participate in and support continuous improvement activities, maintain a clean and organized work space area to ensure compliance.

  • Release of production rooms, along with in-process checks and review/audit of E-log books

  • Entry of engineering work orders, including coordination and tracking of preventive maintenance activities

  • Performing operator-level job responsibilities in production areas as part of cross-functional activities, if needed

Similar jobs, posted recently

Open roles like this one, listed in the last 30 days.

You've read the whole posting — now see how you match it.