Data Specialist

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.

• 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, 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.