MedTech QA Compliance Specialist

globusmedical

Lower Providence Township (PA)

On-site

USD 42,000 - 64,000

Full time

3 days ago
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Job summary

Globus Medical, Inc. is seeking a Quality Assurance Reviewer to join the QA Operations team in Pennsylvania. The role is responsible for reviewing batch records, release decisions, and ensuring documents are properly scanned and logged in the electronic record system.

The successful candidate will generate Excel tracking sheets, verify certificates of compliance and test reports, and adhere to GMP, SOPs, and regulatory requirements while supporting production schedules and quality objectives.

Qualifications

  • Experience with document review and GMP/SOP awareness preferred.
  • High School Diploma or equivalent required.
  • Self-motivated with ability to take initiative and learn continuously.
  • Strong organizational, problem-solving and follow-up skills in a fast-paced environment.

Responsibilities

  • Performs batch record review and release functions.
  • Reviews certificates of compliance or test reports.
  • Reviews receiving inspection documentation.
  • Reports non-conformances and discrepancies.
  • Generates Excel spreadsheets to record review activities.
  • Ensures that completed batch records and other quality documents are scanned and logged in the electronic system.
  • Supports meeting production schedules and adheres to safety SOPs.
  • Maintains compliance with applicable laws, regulations, and company policies.

Skills

Document review
MS Excel
Self-motivated
Attention to detail
Time management

Education

High School Diploma or equivalent

Job description

Globus Medical, Inc. is seeking a Quality Assurance Reviewer to join the QA Operations team in Pennsylvania. The role is responsible for reviewing batch records, release decisions, and ensuring documents are properly scanned and logged in the electronic record system.

The successful candidate will generate Excel tracking sheets, verify certificates of compliance and test reports, and adhere to GMP, SOPs, and regulatory requirements while supporting production schedules and quality objectives.

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