Lead QA Inspector - Cleanroom Medical Devices

ADP, Inc.

Plymouth (MN)

On-site

USD 52,000 - 72,000

Full time

14 days+

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Benefits offered by this job

401k match
Profit sharing
Medical insurance
HSA/FSA
Vision insurance
Life insurance
Paid leave
Disability insurance
Pet insurance

Job summary

ProMed seeks a Quality Assurance Inspector to ensure manufactured parts meet strict standards and to support the supply chain with documentation and process control. The role emphasizes ALCOA++ data integrity, batch record reviews, and QA releases, within a cleanroom environment.

Candidates should have 2–3 years of quality experience, proficiency with SOPs, and the ability to train new inspectors while collaborating across teams.

Qualifications

  • Minimum of 2-3 years of quality experience preferred.
  • ALCOA++ principles knowledge.
  • Experience with eQMS and ERP systems.
  • Ability to read, analyze, and interpret SOPs and work instructions.
  • Ability to train new Inspectors.
  • Experience working in a cleanroom environment.
  • Knowledge of quality events (deviations, investigations, CAPAs).
  • Excellent communication and interpersonal skills.

Responsibilities

  • Performs microscopic, visual and dimensional inspection of manufactured parts using related measuring equipment.
  • Performs line clearance and QA checks as needed.
  • Assist with QA operations such as inspection, issuing deviations, processing non-conforming materials (NCMRs).
  • Assists research and development projects as needed.
  • Assist with batch record review according to procedures.
  • Assist with QA product release tasks.
  • Reviews incoming receipt for all materials.
  • Monitors production line adherence to standards and procedures.

Skills

Quality experience
ALCOA++
eQMS/ERP
SOP reading
Train Inspectors
Cleanroom
Quality events
Communication

Job description

ProMed seeks a Quality Assurance Inspector to ensure manufactured parts meet strict standards and to support the supply chain with documentation and process control. The role emphasizes ALCOA++ data integrity, batch record reviews, and QA releases, within a cleanroom environment.

Candidates should have 2–3 years of quality experience, proficiency with SOPs, and the ability to train new inspectors while collaborating across teams.

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