3rd Shift Microarray Manufacturing Supervisor

DiaSorin S.p.A.

Illinois

On-site

USD 65,000 - 87,000

Full time

14 days+

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Benefits offered by this job

Health benefits
Retirement plan
Time off program

Job summary

Luminex Corporation seeks a Diagnostics Supervisor for 3rd shift manufacturing, overseeing microarray production, personnel, and equipment to ensure compliant, efficient operations per cGMP and QSR. The role includes validation, CAPAs, and investigations to improve quality and throughput.

Responsibilities cover SOP adherence, DMRs/DPRs, DHR approvals, and cross-functional collaboration with Engineering, R&D, QA, and Manufacturing. Requires strong project management and regulatory knowledge.

Qualifications

  • Associate degree or equivalent in Engineering Tech, Industrial Tech, Chemistry or Business.
  • 5+ years related manufacturing experience and/or training.
  • 3+ years of supervisory experience required.
  • Knowledge of cGMP (21 CFR 820, CMDR, ISO 13485) and their impact on manufacturing.
  • Strong computer skills for ERP and manufacturing software.

Responsibilities

  • Supervise the microarray manufacturing team and ensure quality and throughput.
  • Ensure work complies with SOPs and quality systems (DMRs, BPRs, DHRs).
  • Approve lots and related documentation in a timely manner.
  • Assist in equipment validation and calibration.
  • Plan preventive maintenance and calibration of equipment.
  • Lead process improvements and cross-functional collaboration across Engineering, R&D, QA and Production Control.

Skills

Project Management
Quality Assurance
Leadership
Regulatory Compliance
Process Improvement
ERP Systems
MFG Software

Education

Associate's Degree in Engineering Technology
Industrial Technology
Chemistry
Business

Tools

ERP Systems
MFG Software

Job description

Luminex Corporation seeks a Diagnostics Supervisor for 3rd shift manufacturing, overseeing microarray production, personnel, and equipment to ensure compliant, efficient operations per cGMP and QSR. The role includes validation, CAPAs, and investigations to improve quality and throughput.

Responsibilities cover SOP adherence, DMRs/DPRs, DHR approvals, and cross-functional collaboration with Engineering, R&D, QA, and Manufacturing. Requires strong project management and regulatory knowledge.

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