GMP Batch & QC Operations Specialist

Corestaff Services

Durham (NC)

On-site

USD 24,796 - 38,572

Full time

14 days+

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Job summary

Corestaff Services is seeking a GMP manufacturing support professional to assist daily production activities, including batch creation, labeling, and documentation in GLIMS. The role involves coordinating sampling with QC and ensuring data integrity for batch releases.

The ideal candidate will have an Associate's degree, 2–3 years in an admin role in pharma, and familiarity with LIMS/PAS-X and MS Office. Strong communication and organizational skills are essential for successful cross-functional

Qualifications

  • Associate's degree or equivalent combination of education and experience.
  • 2-3 years of experience in an administrative field, preferably in a pharmaceutical environment.
  • Minimum of one year of manufacturing experience in a pharmaceutical environment preferred.
  • Proficient in MS Office (Word, Excel, PowerPoint, Outlook).
  • Experience using LIMS and PAS-X systems preferred.
  • Strong interpersonal, oral and written communication skills required.

Responsibilities

  • Create production batches and print labels in GLIMS to support daily manufacturing operations.
  • Print and review paper batch records to ensure GMP compliance.
  • Enter GMP production data into GLIMS to support batch release activities.
  • Aliquot production samples and deliver to QC lab on time with right-first-time execution.
  • Coordinate daily sampling schedules with stakeholders using the sample tracker.

Skills

Problem solving
Communication
Organizational skills
Team collaboration
Attention to detail

Education

Associate's degree

Tools

Microsoft Office
LIMS
PAS-X

Job description

Corestaff Services is seeking a GMP manufacturing support professional to assist daily production activities, including batch creation, labeling, and documentation in GLIMS. The role involves coordinating sampling with QC and ensuring data integrity for batch releases.

The ideal candidate will have an Associate's degree, 2–3 years in an admin role in pharma, and familiarity with LIMS/PAS-X and MS Office. Strong communication and organizational skills are essential for successful cross-functional

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