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 a Film Electrical Manufacturing Engineer III. The Film Electrical Manufacturing Engineer III will provide engineering oversight of film coating equipment and supporting systems to effectively and efficiently maintain and reliably operate the manufacturing equipment on site. Strong focus will be on troubleshooting and managing electrical systems and components throughout their lifecycle including repairs, replacements, and upgrades. This position involves collaboration with various departments to ensure product compliance and continuity, to manage supply chain risks, and to validate components all while upholding the companies core values in interactions with team members and reporting to the Engineering Manager. A successful candidate will play a vital role in the overall success of operations.
This position also requires system and process assessment, control of operating and maintenance documentation including performance metrics, attainment of productivity and cost objectives in daily operation, and assisting in maintenance of all equipment as needed in assigned areas and field. This position will continuously assess the general condition and validated readiness of critical assets required to deliver high quality, safe, compliant, cost effective equipment processes without interruption.
This position is in Rochester, NY.
The Responsibilities
Support Maintenance and Operations with troubleshooting and resolving electrical issues on current automated equipment.
Lead or support large capital projects for equipment upgrades or replacements as required.
Identify and develop improvements to maximize uptime while reducing maintenance costs and improving reliability, quality, productivity, and safety.
Author and revise controlled manufacturing documentation such as preventative maintenance and standard operatizing procedure documents per ISO9000 standards.
Develop and maintain effective lines of communication across departments to achieve plant maintenance and reliability goals.
The Individual
Required:
BS or MS in Electrical Engineering or Electrical Engineering Technology3-5 years of experience in an automated manufacturing support or automation build role, specifically with electrical systems and components.
Strong electrical aptitude with troubleshooting experience.
Strong verbal and written communication.
Ability to plan, analyze, review, and implement assignments without appreciable guidance.
Ability to manage competing priorities in a results-driven environment.
Ability to lead teams and meet project deadlines.
Adept in "Good Manufacturing Practices" (GMP).
Adept in Microsoft Office tools (e.g. Word, Excel, PowerPoint, etc.).
Preferred:
Experience working in an FDA medical device manufacturing facility with associated FDA and ISO regulations.
Experience with motor drive systems, process controls systems, manufacturing equipment and vision systems.
The Work EnvironmentThe work environment characteristics are representative of a laboratory and manufacturing environment and include handling of potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids and/or samples. Manual dexterity to handle instruments, complete repetitive motions, and stand for long periods of time is required. Diligent use of PPEs (Personal Protective Equipment) to limit exposure to bloodborne pathogens is required. Up to 75% of time spent in the lab, standing for extended periods of time. Flexible work hours to meet manufacturing deadlines.
Salary TransparencySalary 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 that facts and circumstances of each case. Salary range for this position is $80,000 to $136,000 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.
Equal Employment OpportunityQuidelOrtho 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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