QA Lab Documentation Specialist - Quality Records & Release

ACTalent; Irving (TX); In loco; USD 28.000 - 33.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Time Off / PTO

HSA

Descrizione del lavoro

ACTalent is seeking a QA Lab Documentation Specialist to support laboratory documentation and quality operations in a manufacturing environment. The role emphasizes maintaining accurate quality records, reviewing manufacturing documentation, and supporting product release.

You will review and update QA/lab documents, document lab results, and track quality records using management systems. Strong attention to detail and communication skills are essential for success in this contract role based

Competenze

• High school diploma or equivalent.
• 1+ year QA, QC, laboratory, manufacturing, or documentation experience preferred.
• Strong attention to detail and documentation accuracy.
• Comfortable working with computerized document/records management systems.
• Experience in pharmaceutical, medical, or FDA-regulated manufacturing is a plus.
• Strong written and verbal communication skills.

Mansioni

• Maintain and update controlled QA/laboratory documents.
• Review manufacturing records for accuracy and completeness.
• Document laboratory test results according to QA procedures.
• Prepare testing and product release documentation.
• Use document and records management systems to track quality records.
• Identify documentation errors or quality issues and escalation when needed.
• Follow established QA procedures and FDA-related requirements.
• Support general laboratory testing and quality activities as needed.

Conoscenze

Attention to detail

Documentation accuracy

Written communication

Verbal communication

Detail-oriented

Formazione

High school diploma or equivalent

Descrizione del lavoro

ACTalent is seeking a QA Lab Documentation Specialist to support laboratory documentation and quality operations in a manufacturing environment. The role emphasizes maintaining accurate quality records, reviewing manufacturing documentation, and supporting product release.

You will review and update QA/lab documents, document lab results, and track quality records using management systems. Strong attention to detail and communication skills are essential for success in this contract role based