Senior Process Controls Engineer

The Opportunity

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics creating a worldleading in vitro diagnostics company with awardwinning 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 a Senior Process Controls Engineer. The Senior Process Controls Engineer is an integral member of the Rochester Microwell Mfg. Team. This position will support a high speed automated manufacturing operation and the associated engineering and maintenance functions when required to troubleshoot high level issues when impacting production. Additionally the Senior Process Controls Engineer shall be responsible for conducting thorough testing and validation of control systems to ensure compliance with industry standards safety regulations and performance criteria. Troubleshooting and resolving technical issues related to control systems will be a critical aspect of your role requiring strong analytical and problemsolving skills. Additionally you will provide technical support and training to operations and maintenance personnel ensuring they understand system functionalities and can effectively manage system operations. The successful candidate will stay abreast of emerging technologies and industry trends continuously seeking opportunities to improve existing systems and processes. You will participate in project planning and management activities including budgeting scheduling and resource allocation to ensure timely and costeffective project delivery. Your ability to communicate effectively with stakeholders clients and team members will be essential in facilitating successful project outcomes. Your contributions will directly impact the efficiency safety and sustainability of critical industrial operations.

This position is located in Rochester NY.

The Responsibilities

• Responsible for implementing and maintaining control systems to optimize industrial processes ensuring efficiency safety and reliability.

• Collaborate closely with multidisciplinary teams including production maintenance and quality assurance to identify areas for improvement and implement innovative solutions.

• Play a critical role in analyzing existing processes identifying bottlenecks and developing strategies to enhance productivity and reduce operational costs.

• Keep abreast of new technical developments affecting the organization for an assigned area of responsibility.

• Formulate strategies for the development of programs that bring new and improved engineering technology into the company.

• Initiates leads and supports cost improvement projects and business continuity initiatives.

• Maintains clear communication with internal and external business partners regarding expectations satisfaction and/or quality of results.

• Consults with maintenance to draft maintenance procedures for new designs developing troubleshooting techniques creation of preventative maintenance (PM) schedules and providing recommended spare parts lists.

• Expertise will be essential in troubleshooting complex control system issues performing root cause analysis and recommending corrective actions.

• Ensure compliance with industry standards safety regulations and environmental guidelines.

• Regular interaction with equipment suppliers contractors and internal stakeholders to ensure seamless integration and operation of control systems.

• Provide training and technical support to operations and maintenance personnel ensuring they understand and effectively utilize the control systems.

• Possess strong analytical and problemsolving skills excellent communication abilities and a proactive approach to continuous improvement.

• Comfortable working independently and collaboratively managing multiple projects simultaneously and adapting quickly to changing priorities and challenges.

• Assist in determining objectives and planning schedules of specific task within a given project / activity; apply comprehensive and diverse knowledge of engineering / business principles to a broad range of assignments.

• Coordinates and directs activities of other technical support staff and delegates their assignments as required.

• Performs other workrelated duties as assigned.

The Individual

Required:

• Minimum of 3 years of experience in Process Control Engineering.

• Proficiency in PLC programming SCADA systems and automation technologies.

• Strong electrical & mechanical aptitude with troubleshooting experience.

• Adept with MicroSoft Office tools (e.g. Word Excel Project PowerPoint etc..

• Ability to manage competing priorities in a resultsdriven environment is essential.

• Working knowledge and understanding of pneumatic systems and pneumatic logic is also required to support the operations.

• Executes the validation process including conducting design reviews prevalidation assessments and installation operational and process qualifications.

Preferred:

• Direct experience with motor drive systems process controls systems manufacturing equipment and vision systems.

• Control Networking experience (Ethernet/IP DeviceNet ControlNet) and familiarity with databases.

• Experience working in an FDA Medical Device Manufacturing Facility with associated FDA and ISO regulations.

The Key Working Relationships

Internal: Operations Maintenance Facilities and Environmental Health & Safety Quality and Regulatory

External: Suppliers

The Work Environment

The work environment characteristics are representative of an office environment. Up to 75 of time at desk standing or sitting extended periods of time. No strenuous physical activity though occasional light lifting of files and related materials (up to 10 lbs. is required.10 travel overall (including International) but could require up to 50 travel for short durations during commissioning of new equipment at suppliers.

Salary Transparency

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 that facts and circumstances of each case. Salary range for this position is $94000 to $159000 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 noncontractual 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 .

#LISP1