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Job Requirements of Quality Analyst I:
-
Employment Type:
Contractor
-
Location:
Rochester, NY (Onsite)
Do you meet the requirements for this job?
Quality Analyst I
Careers Integrated Resources Inc
Rochester, NY (Onsite)
Contractor
Job Title: Quality Analyst I
Location: Rochester, NY
Duration:12 months+ (Possibilities of Extension)
Shift details M-F, 40 hrs/week, 2-week rotations between A shift (7 am - 3:30 pm) and B shift (1:30 pm – 10 pm).
Pay Rate: $25/hr. on w2
Responsibilities:
Qualifications:
#sczr2
Location: Rochester, NY
Duration:12 months+ (Possibilities of Extension)
Shift details M-F, 40 hrs/week, 2-week rotations between A shift (7 am - 3:30 pm) and B shift (1:30 pm – 10 pm).
Pay Rate: $25/hr. on w2
Responsibilities:
- Working in a laboratory environment supporting the manufacturing operations, this person will be responsible for executing release testing and data analysis for release of product.
- Individual will run, maintain, and troubleshoot, FS 5,1, 4600, and 3400XT 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 execute testing following Test Designs and analyze data for the release of product.
- Routinely interacts with data management systems such as LIMS, SAP, Document Management Systems (Windchill), and Non-Conformance & CAPAs (QERTS).
Qualifications:
- A BA/BS Degree or equivalent is required.
- A Degree in science concentration is preferred.
- 1-2 years experience.
- Previous laboratory or similar experience is required.
- Candidate must be willing to learn to operate, maintain and troubleshoot, FS 5,1, 3400, and 4600 analyzers.
- Candidate must have analytical knowledge required for production releases.
- Experience in QO LIMS or SAP is preferred.
- 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, candidate must have an understanding of cGMPs and documentation in a regulated industry.
- Experience in documentation protocols and procedures are a plus.
- 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.
- 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.
#sczr2
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