Operator, Film Coating

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 we continue to grow as QuidelOrtho we are seeking an Operator II Film Coating to perform operations as described by our Standard Operating Procedures (SOPs) under Good Manufacturing Practices (GMPs) in our Film manufacturing Department located in Rochester NY. You will prepare sets-up and assemble components needed for production visually inspect components for defects operate and troubleshoot equipment issues while strictly following all regulations and requirements including cGMPs OSHA FDA and ISO regulations.

This opportunity is located in Rochester NY.

Work Schedule: Ability to work a varying schedule of shifts (combination A-B-C) is required.

The Responsibilities

• Responsible for using equipment for the assembly and processing tasks to produce finished products according to established specifications.

• Accountable for adhering to all quality and safety guidelines.

• Effectively communicates verbally and in writing.

• Demonstrates a sense of urgency to complete production schedule on time.

• Accepts personal responsibility for the quality and timeliness of work.

• Accurately and timely completes all required reporting functions.

• Uses computer based documentation system to find view and print specifications and procedures.

• Disposes of scrap/rejected material in appropriate manner and according to safety regulations.

• Clean and assemble equipment while following safety procedures and practices and maintaining a clean orderly work environment.

• Disposes of hazardous materials appropriately operates machinery and interacts with computer controlled equipment and processes.

• Conducts basic quality inspection of work in accordance with statistical process or other control procedures.

• Participates in projects focused on process development and/or improvement cost controls and new product manufacturing.

• Ability to work in a team environment.

The Individual

• A High School Diploma or GED is required.

• Strong mechanical aptitude troubleshooting of equipment is required.

• The ability to read and write in English is required.

• A minimum of 3 months experience in operations/manufacturing environment (prefer a regulated industry).

• Must have basic computer skills i.e. Microsoft Office (Word Excel outlook).

• Experience with quality information systems (i.e. SAP) is preferred.

• Knowledge and experience with GMP/ISO regulations is preferred.

Key Working Relationships

Internal Partners: Maintenance Engineering Quality

External Partners: Suppliers

Work Environment

The work environment characteristics are representative of a manufacturing laboratory or warehouse environment and include handling of viral and bacterial hazards potentially hazardous chemicals as well as infectious or potentially infectious bodily fluids tissues and samples. Up to 75% of the time you will be standing walking or sitting bending and stooping for extended periods of time. Ability to lift up to 35 lbs. Manual dexterity for manipulating parts and repetitive motions are required. Flexible work hours to meet project deadlines.

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. At QuidelOrtho it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range is $48000.00 to $62000.00 and is bonus eligible. 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 Employment 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 their 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

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