Pharma Documentation & Quality Control Specialist

ARUP Laboratories; Salt Lake City, Northern (UT, KY); Hybrid; USD 50,000 - 70,000; Full time

Job summary

ARUP Laboratories is seeking a detail‑oriented Document Control Specialist to manage the update, review, and storage of PharmaDx department controlled documents in MasterControl. You will coordinate workflows, ensure current revisions, and support audits and inspections.

You will train others, maintain compliance with ISO, FDA, IVDR, CAP/CLIA, and GMP standards, and contribute to continuous improvement within the PharmaDx team in Salt Lake City.

Qualifications

• High School Diploma or equivalent required.
• Associates Degree or better preferred.
• Basic skills with Microsoft Office Suite required.

Responsibilities

• Maintains and updates controlled documents in MasterControl for PharmaDx.
• Provides training in MasterControl within PharmaDx.
• Manages document workflows and approvals to ensure prompt completion.
• Ensures regulatory standards are maintained in PharmaDx document control.
• Assists Audit/Inspection preparation for PharmaDx.
• Prints, prepares, and stores PharmaDx batch records for manufacturing use.
• Trains and mentors other PharmaDx Document Control Specialists.
• Participates in PharmaDx project/improvement teams and presents updates.

Skills

Basic Microsoft Office

Education

High School Diploma or equivalent

Associates Degree or better

Job description

ARUP Laboratories is seeking a detail‑oriented Document Control Specialist to manage the update, review, and storage of PharmaDx department controlled documents in MasterControl. You will coordinate workflows, ensure current revisions, and support audits and inspections.

You will train others, maintain compliance with ISO, FDA, IVDR, CAP/CLIA, and GMP standards, and contribute to continuous improvement within the PharmaDx team in Salt Lake City.