Data Specialist

Insight Global; Raritan (NJ); On-site; USD 65,000 - 90,000; Full time

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

• Bachelor's or associates Degree in scientific field
• 1+ years experience working in a GMP or Pharmaceutical lab environment
• Strong excel experience
• Electronic batch record experience
• MES system experience as an end user

Job Description

Our global pharmaceutical client is seeking a Documentation & Data Compliance Specialist to support ongoing manufacturing and quality systems initiatives. This individual will play a key role in reviewing, reconciling, and validating data across multiple documentation sources and electronic systems to support process improvement and compliance efforts.

Responsibilities include performing detailed data reviews, verifying information against source documentation, supporting controlled document updates, and collaborating with Quality, Manufacturing, and Operations teams during ongoing digital transformation projects. The ideal candidate has experience working in a regulated environment, strong attention to detail, and exposure to GMP documentation, batch records, electronic systems, or quality management platforms.

This position requires strong Excel skills, the ability to manage large volumes of data with accuracy, and comfort working cross-functionally in a fast-paced manufacturing environment. This is an onsite role requiring 5 days per week on site.