Quality Control Sampling & Incoming Inspection Manager

GE HealthCare Technologies

Base: $95,040.00-$142,560.00 annual; bonus/equity:...
Not specified (assumed to be onsite due to the nature of the role).
Gmp regulatory compliance (21 cfr 210/211)
Raw material sampling and inspection
Alcoa+ data integrity principles
The Quality Control Sampling & Incoming Inspection Manager position at GE HealthCare Technologies involves overseeing the inspection and sampling of raw materials in a GMP-regulated pharmaceutical manufacturing environment. The role requires strong leadership, compliance knowledge, and the ability to collaborate across various functions to ensure material quality and regulatory adherence

Job Summary

  • The manager oversees all activities related to the sampling and inspection of raw materials, components, and packaging materials in a GMP regulated pharmaceutical manufacturing facility.
  • This role ensures timely material release, maintains data integrity, and partners closely with Production, QC Analytical Chemistry, QC Microbiology, QA, and Warehouse Operations.
  • GE HealthCare offers a competitive benefits package including medical, dental, vision, paid time off, a 401(k) plan, and tuition reimbursement.

Matching Summary

Match Score: 85

The Quality Control Sampling & Incoming Inspection Manager position at GE HealthCare Technologies involves overseeing the inspection and sampling of raw materials in a GMP-regulated pharmaceutical manufacturing environment. The role requires strong leadership, compliance knowledge, and the ability to collaborate across various functions to ensure material quality and regulatory adherence.

Salary

Base: $95,040.00-$142,560.00 Annual; Bonus/Equity: Performance based incentive compensation available; Benefits: Medical, dental, vision, 401(k), PTO, tuition reimbursement

Skills & Requirements

Must-have

  • GMP regulatory compliance (21 CFR 210/211)
  • Raw material sampling and inspection
  • ALCOA+ data integrity principles
  • SOP authoring and review
  • Deviation and OOS investigation leadership
  • LIMS and SAP system proficiency

Nice-to-have

  • Continuous improvement initiatives
  • New sampling technology evaluation
  • Cross-functional team collaboration
  • Risk reduction strategies
  • Supplier qualification support

Key Requirements

  • Bachelor's degree preferred or Associate degree with experience
  • 5-8+ years in pharmaceutical/biotech QC or materials testing
  • 2+ years of supervisory or management experience
  • Strong working knowledge of FDA, EMA, ICH guidelines
  • Authorized to work in the United States (no sponsorship)

Work Rights

Must be legally authorized to work in the US

Tailored Resume

Cover Letter