Quality/QMS Engineer- Maumelle, AR - Georgia IT Inc.
Maumelle, AR
About the Job
Job Title: Quality/QMS Engineer
Location: Maumelle, AR
Position Type: Contract
Work Status: US Citizen/Green Card
Rate: $45/hr W2 only (DOE)
Candidates must be Certified Internal auditor and have experience in cosmetic/medical device industry.
Ensure compliance to quality procedures / processes. Conduct product quality tests, compliance and process audits. Evaluate quality performance. Investigate quality issues and implement corrective actions. Expert position that requires a Bachelors or Masters degree and 8-10 years of experience.
A Quality/QMS Engineer Must have thorough knowledge of QMS systems including CAPA and QNC, Internal Audits, Calibration, Change Management, Validation, Good Manufacturing Practices (GMP), and must have experience with QMS improvement programs. They will be expected to drive improvements in the mill QMS. They may assist with completing validations, as well as help review/ write procedures and work instructions. They will be expected to help provide training on new procedures to a variety of people including operators, quality team members, engineers and leadership team members. They must have internal auditor certifications (such as ASQ or equivalent), Experience with FDA inspections and response plans is highly desirable. Open to candidates with less than 10 years of experience if they have a solid background.
Location: Maumelle, AR
Position Type: Contract
Work Status: US Citizen/Green Card
Rate: $45/hr W2 only (DOE)
Candidates must be Certified Internal auditor and have experience in cosmetic/medical device industry.
Ensure compliance to quality procedures / processes. Conduct product quality tests, compliance and process audits. Evaluate quality performance. Investigate quality issues and implement corrective actions. Expert position that requires a Bachelors or Masters degree and 8-10 years of experience.
A Quality/QMS Engineer Must have thorough knowledge of QMS systems including CAPA and QNC, Internal Audits, Calibration, Change Management, Validation, Good Manufacturing Practices (GMP), and must have experience with QMS improvement programs. They will be expected to drive improvements in the mill QMS. They may assist with completing validations, as well as help review/ write procedures and work instructions. They will be expected to help provide training on new procedures to a variety of people including operators, quality team members, engineers and leadership team members. They must have internal auditor certifications (such as ASQ or equivalent), Experience with FDA inspections and response plans is highly desirable. Open to candidates with less than 10 years of experience if they have a solid background.
Source : Georgia IT Inc.