Operator II

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 6,000 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 cGMP's, 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.

• 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.

Required:

• High School Diploma, GED, or equivalent work experience 3+ years.

• 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).

• The ability to read and write in English.

• Strong mechanical aptitude, troubleshooting of equipment.

• Physical work condition demands for the position include standing, bending and stooping -some lifting not to exceed 35 pounds.

• Manual dexterity for manipulating parts and repetitive motions.

• Ability to work a varying schedule of shifts (combination A-B-C).

Preferred:

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

• Knowledge and experience with GMP/ISO regulations.

Key Working Relationships

Internal Partners: Maintenance, Engineering, Quality

External Partners: Suppliers

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.

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 for this position is $36,000 to $62,000 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.

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 recruiting@quidelortho.com.

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