Hybrid Quality Manager: Lead QMS, Audits & CI

Equilibar Llc

Fletcher (NC)

Hybrid

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Equilibar is seeking a Quality Manager to maintain and continuously improve the company’s QMS, ensuring products, processes, and customer solutions meet requirements. You will collaborate across Engineering, Production, and Customer Support, driving root-cause analysis, corrective actions, and preventive measures.

The role emphasizes hands-on problem solving, audit excellence, and development of the quality team, with a focus on regulated industries such as biopharmaceutical manufacturing.

Qualifications

  • Bachelor’s degree in engineering, business, or related field; advanced degree preferred.
  • Experience leading or developing quality personnel.
  • Experience with ISO-based QMS in engineering/manufacturing.
  • Experience with root-cause analysis, corrective actions and nonconformances.
  • Experience conducting internal and external quality audits.

Responsibilities

  • Maintain and support Equilibar’s QMS and ensure quality processes are followed.
  • Coordinate quality activities, audits, CAPA, risk management and training.
  • Lead investigations using structured root-cause analysis and corrective actions.
  • Support process owners in addressing audit observations and customer quality reviews.
  • Work with customers and suppliers to ensure quality expectations.

Skills

Quality leadership
Root cause analysis
Cross-functional collaboration
Audit management
Documentation & records
Problem solving

Education

Bachelor’s degree in engineering, business, or related field
Advanced degree preferred

Job description

Equilibar is seeking a Quality Manager to maintain and continuously improve the company’s QMS, ensuring products, processes, and customer solutions meet requirements. You will collaborate across Engineering, Production, and Customer Support, driving root-cause analysis, corrective actions, and preventive measures.

The role emphasizes hands-on problem solving, audit excellence, and development of the quality team, with a focus on regulated industries such as biopharmaceutical manufacturing.

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