VetJobs - The Leading Military Job Board

qa specialist - dhr reviewer.

• latham , new york

• posted april 26, 2024

job details

summary

• $25 - $30 per hour

• temporary

• high school

• category office and administrative support occupations

• referenceAB_4523202

job details

Quality Assurance Specialist - Device History Record (DHR) Are you a self-starter but also great in a team setting with superb attention to detail? The QA Specialist – DHR Reviewer is a member of the Manufacturing Quality team within the Philips MRI magnet manufacturing facility in Latham, NY. This is an onsite role which ensures compliance with legal, regulatory and international standards as they to Latham's Quality Management System. This individual ensures Device History Records meet regulatory and internal requirements and provide adequate verification of compliance to the product's engineering specifications.

salary: $25 - $30 per hour

shift: First

work hours: 8 AM - 4 PM

education: High School

Responsibilities

In this role you are responsible for:

• Reviewing and approving of executed DHR packages (electronic & paper record) and ensuring the data is in compliance with relevant specifications, parameters and tolerances in accordance with local procedures, regulatory requirements and international standards.

• Reviewing data recorded in the Manufacturing Execution System (MES) to ensure compliance with relevant specifications, parameters and tolerances in accordance with local procedures, regulatory requirements, and international standards.

• Identifying areas for improvement within DHR process and data collection to optimize execution and efficiency.

• Executing in-line DHR reviews to proactively identify risks or nonconformances.

• Identifying non-conformances and taking appropriate actions to correct issues through Non-conforming Process.

• Reviewing proposed or revised DHR data collects to ensure compliance with relevant specifications, local procedures, regulatory requirements and international standards.

• Supporting nonconformance investigations, as required, to drive root cause and corrective actions in Operations.

• Providing Quality Engineers with support and data, as needed, to improve Quality on manufactured products.

Skills

• Quality Control (1 year of experience is required)

• Medical Device Manufacturing (1 year of experience is preferred)

• GMP/GCP (1 year of experience is preferred)

Qualifications

• Years of experience: 1 year

• Experience level: Experienced

Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

Applications accepted on ongoing basis until filled.

get in touch

we are here to help you with your questions.

JN

jesse nagler

• jesse.nagler@randstadusa.com