Quality Technician III
Quality Technician III
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Job Description
The Opportunity
QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing clinical chemistry and transfusion medicine. We are more than 6000 strong and do business in over 130 countries providing answers with fast accurate and consistent testing where and when they are needed most home to hospital lab to clinic.
Our culture puts our team members first and prioritizes actions that support happiness inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.
The Role
As the company continues to grow we are seeking a Quality Technician III for Device History Record (DHR) review and Incoming Inspection. This position is located in Rochester NY supporting the three (3) full-time position will be 40 hours per week (5 x 8-hour shifts) from 07:00am -03:30pm (A shift). The potential scheduled workdays are Monday to Friday with occasional Saturday and Sunday coverage as needed.
The Responsibilities
Reviews raw material Certificates of Analysis and Certificates of Conformance for acceptance.
Inspects raw materials for compliance against specifications.
Reviews Device History Records (DHRs) and Incoming Inspection documentation for accuracy completeness and compliance per applicable departmental procedures.
Responsible for maintaining Incoming Inspection and DHR records and documentation filing storage and logging for shipment to storage facility.
Ability to learn and execute Change Control to document and implement revisions of documents associated with the role.
Ability to observe and participate in cross-functional discussions meetings and product reviews to learn and support nonconformances and corrective actions.
Maintains a record of Incoming Inspections and DHR metrics to be presented at quality forums.
Generates nonconformances respective to work area when required and accountable to escalate quality concerns or issues to management.
Work 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.
Perform other work-related duties as assigned.
The Individual
Minimum of BA/BS degree or 3 years experience is required.
Knowledge and application using Microsoft Office (Excel Word Outlook Teams PowerPoint).
Must be detail oriented having the ability to work both independently and as part of a dynamic team.
Ability to communicate effectively at all levels across the business; effective verbal and written communication.
Must work well in an environment with defined production deadlines and changing business needs.
Travel between the three Rochester facilities (within a 2 mile radius from each other).
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 good documentation practices in a regulated industry.
This position is not currently eligible for visa sponsorship.
The Key Working Relationships
Internal Partners: Quality Product Support PP&L/Materials Management Operations
External: Suppliers
The Work Environment
Manufacturing laboratory or warehouse setting.
Exposure to viral and bacterial hazards hazardous chemicals and potentially infectious materials.
Flexible work hours to meet project deadlines.
The Physical Demands
Light
Sitting standing walking.
Computer
Salary Transparency
The salary range for this position takes into account a wide range of factors including education experience knowledge skills geography and abilities of the candidate in addition to internal equity and alignment with market data. The salary range for this position is $25/hour to $30/hour. QuidelOrtho offers a comprehensive benefits package including medical dental vision life and disability insurance along with a 401(k) plan employee assistance program Employee Stock Purchase Plan paid time off (including sick time) and paid Holidays. All benefits are non-contractual and QuidelOrtho may amend terminate or enhance the benefits provided as it deems appropriate.
Equal Opportunity
QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals including individuals with disabilities have an opportunity to apply for those positions that they are interested in and qualify for without regard to race religion color national origin citizenship sex sexual orientation gender identity age veteran status disability genetic information or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability please contact us at .
#LI-AC1
Required Experience:
IC
Employment Type
Full-Time
