GMP Data Integrity & Compliance Specialist

Insight Global

Raritan (NJ)

On-site

USD 65,000 - 90,000

Full time

2 days ago

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Job summary

Insight Global is seeking a Documentation & Data Compliance Specialist for our global pharmaceutical client to support ongoing manufacturing and quality systems initiatives. You will review, reconcile, and validate data across multiple documentation sources and electronic systems to support process improvement and compliance efforts.

Responsibilities include detailed data reviews, verifying information against source documentation, updating controlled documents, and collaborating with Quality,

Qualifications

Bachelor's or associate's degree in scientific field.
1+ years experience in GMP or Pharmaceutical lab environment.
Strong Excel experience.
Electronic batch record experience.
MES system experience as an end user.

Responsibilities

Review, reconcile, and validate data across documentation sources and electronic systems to support process improvement and compliance efforts.
Perform detailed data reviews, verify information against source documentation, and support controlled document updates.
Collaborate with Quality, Manufacturing, and Operations during digital transformation projects.
Handle large volumes of data accurately in a fast-paced manufacturing environment and cross-functional teamwork.

Skills

Excel

Electronic batch records

MES system

GMP environment

Documentation management

Education

Bachelor's or Associate's degree in scientific field

Tools

MES system

Job description

Responsibilities include detailed data reviews, verifying information against source documentation, updating controlled documents, and collaborating with Quality,

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