Skills

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Education/Persona
Degree Type Major/Certification Required Preferred Bachelor's Degree Science
Job Description & Requirements
Job Type: Recruited Resource - General Temp Number of Positions: 1 System Location: QO - 1001 Created Date: 6/4/2024 Job Title: Quality Analyst I CWR Type: W-2 Reason: Resignation/Open Position
Responsibilities:

QuidelOrtho serves the transfusion medicine community and laboratories around the world. We're a leading provider of total solutions for screening, diagnosing, monitoring, and confirming diseases early, before they put lives at risk. Our single focus is to help hospitals, laboratories and blood centers worldwide deliver results that help patients experience a better quality of life.

Working in a laboratory environment supporting manufacturing operations, this individual will be responsible for executing release testing and data analysis for release of product. The individual will run, maintain, and troubleshoot Vitros 350, FS 5,1, 3400XT, and 4600 analyzers. This position works in partnership with manufacturing Operations, Product Support, and other technical support groups to ensure Quality and customer expectations are met prior to final release of the product. The individual will routinely interact with Document Management Systems (Windchill).

Candidate must be willing to learn to operate, maintain, and troubleshoot Vitros 350, FS 5,1, 3400XT, and 4600 analyzers. Careful attention to detail and accuracy of work are required. As an FDA-regulated facility, documentation is key to this position in order to meet regulatory requirements; therefore, the candidate must have experience in or an understanding of cGMPs and documentation in a regulated industry. Candidate must have a proven track record of planning and organization of daily workload, high affinity toward teamwork, and demonstrated problem-solving using innovative solutions. Having a working knowledge of computers and Windows software is desired. A full understanding of quality control is expected. This position requires an individual who can multi-task, adapt to changes in daily workload and priorities, and operate in a cross-functional team setting. This position requires working in a BL2 lab environment which includes standing for long periods of time, wearing personal protective equipment (PPE), and handling human samples.
Qualifications:

BA/BS degree or equivalent is required; a degree with a science concentration is preferred. Previous laboratory or similar experience is preferred.

QuidelOrtho is recruiting for a Quality Analyst 1 located in our Quality Release Laboratories in Rochester, NY. This position requires flexibility between A-shift (~7:00am -3:30pm) and B-shift (1:30pm -10:00pm) Monday-Friday.
Requestor & Work Location
Requested by: N/ lternate: N/ Report To: N/ Phone: N/ Ext.:N/ Travel Required: How Much Travel? Report To Manager's Office Address 513 Technology Boulevard USRO2, Rochester, NY 14626 United States Start Date: 6/17/2024 Work Days: Sun Mon Tue Wed Thu Fri Sat End Date: 6/17/2025 Start Time: 3:00 PM Total Reg Hours: 40.00 End Time: 11:30 PM Overtime Required: Lunch Time: 30 Minutes Exempt: Open Bid:

Attachment:

QA Analyst I (Contract) Release Lab - A/B Shift

QuidelOrtho is recruiting for a Quality Analyst 1 located in our Quality Release Laboratories in Rochester, NY. This position requires flexibility between A-shift (~7:00am -3:30pm) and B-shift (1:30pm -10:00pm) Monday-Friday.

QuidelOrtho serves the transfusion medicine community and laboratories around the world. We're a leading provider of total solutions for screening, diagnosing, monitoring, and confirming diseases early, before they put lives at risk. Our single focus is to help hospitals, laboratories and blood centers worldwide deliver results that help patients experience a better quality of life.

Working in a laboratory environment supporting manufacturing operations, this individual will be responsible for executing release testing and data analysis for release of product. The individual will run, maintain, and troubleshoot Vitros 350, FS 5,1, 3400XT, and 4600 analyzers. This position works in partnership with manufacturing Operations, Product Support, and other technical support groups to ensure Quality and customer expectations are met prior to final release of the product. The individual will routinely interact with Document Management Systems (Windchill).
Qualifications:
BA/BS degree or equivalent is required; a degree with a science concentration is preferred. Previous laboratory or similar experience is preferred.

Candidate must be willing to learn to operate, maintain, and troubleshoot Vitros 350, FS 5,1, 3400XT, and 4600 analyzers. Careful attention to detail and accuracy of work are required. As an FDA-regulated facility, documentation is key to this position in order to meet regulatory requirements; therefore, the candidate must have experience in or an understanding of cGMPs and documentation in a regulated industry. Candidate must have a proven track record of planning and organization of daily workload, high affinity toward teamwork, and demonstrated problem-solving using innovative solutions. Having a working knowledge of computers and Windows software is desired. A full understanding of quality control is expected. This position requires an individual who can multi-task, adapt to changes in daily workload and priorities, and operate in a cross-functional team setting. This position requires working in a BL2 lab environment which includes standing for long periods of time, wearing personal protective equipment (PPE), and handling human samples.

This position is located in Rochester, NY.