Staff Engineer

QuidelOrtho
$100,000 - $125,000 annually. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life,
paid time off, paid holidays, sick time, 401(k)
United States, New Jersey, Raritan
1001 U.S. 202 (Show on map)
Mar 26, 2025
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 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 one QuidelOrtho, we are seeking a Manufacturing Engineer IV, responsible for supporting new/existing equipment and processes located at the Raritan, NJ site. This position will be responsible for applying extensive and diversified knowledge of electronic principles and practices in a broad range of assignments and related fields. Makes decisions regarding engineering problems and methods and represents the company in conferences to solve problems and to plan and coordinate work. Responsible for the engineering and quality assurance of part of a major project or for a complete small project. This position is onsite in Raritan, NJ. The Responsibilities Design and selection of new facility and production systems, modifications and upgrades to existing equipment, preparation of capital estimates, generation of capital funding, control of project budgets, timely execution of new installations, equipment commissioning and validation, development and periodic review of standard operating procedures and specifications, maintenance specifications, documentation revision control, and project scheduling and coordination to meet all performance requirements including cost, quality, maintenance, safety and environmental criteria. Work in direct support of the Raritan business operating units to support equipment design and purchases, upgrades, and process improvements. Responsibilities will include developing, coordinating, documenting, and delivering equipment and upgrades with the associated regulatory and change management actions related to projects. Provide the manufacturing team direct support in routine problem solving of a moderate to complex nature and identifying and correcting technical issues for all production shifts, as required. Manage contractors, provide maintenance staff direction on projects, and coach subordinate engineers. cGMP responsibilities will include owning and managing quality events related to process, manufacturing facility equipment issues, corrective/preventive actions, and equipment /process validations. Provide technical support and interact with regulatory agencies during site audits. Must possess strong electrical knowledge and ability to decipher PLC code for troubleshooting The Individual Minimum requirement of a Bachelor's degree in Electrical Engineering and (7- 10) years of medical device and/or pharmaceutical manufacturing process and associated project management experience. Advanced degree preferred. Demonstrated ability to quantify, document, and evaluatefunctional requirements for production and facility systems. Demonstrated skills in development, writing, and executing cGMP-based process and equipment validations. System design knowledge specifically in the following areas is required:Building Automation Systems, PLC programming, vision systems, labeling equipment, servo motors, motion control and automated filling, packaging and assembly equipment. Demonstrated written and verbal communications skills in formulating and communicating technical objectives into viable capital projects as well as interpreting and communicating technical content related to system design, function, and performance to management and auditing agencies. Knowledge of FDA and other regulatory guidance is required (inclusive of participation in commissioning, qualification and validation activities). The candidate is required to be proficient in Microsoft MS Office (Word, Excel, Project, Outlook and PowerPoint), and AutoCAD. Possess the knowledge of Six Sigma methodology for this role. Display a sense of urgency. Share and train on technical information with individuals / groups. Skilled in good documentation practices (cGMP & Maintenance documentation) Available to work on other shifts, if required. Must be able to work independently with minimum supervision, be detail oriented, self-motivated/proactive and work well/interact with other individuals/groups. Must have Ariba purchasing system experience in purchase, receipt, and reconciliation of purchases.. The position will require 5-10% travel and will be located at Raritan, NJ. This position is not currently eligible for visa sponsorship. Key Working Relationships Internal - Operations, Materials Management, Quality, EHS, Facilities, Engineering, Product Support External- Suppliers The Work Environment The work environment characteristics are representative of an office, manufacturing and clean room environment. The Physical Demands Needs to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position. Is frequently required to communicate with coworkers. While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; climb, bend and stoop; and reach with hands and arms. Ability to lift up to 40 lbs. Work with blood, blood products and chemicals. Work in a cGMP area and/or clean room environment. Must pass vision acuity test for inspection of work in process and finished goods. Overtime is required, as necessary. Ability to occasionally work other Shifts may be required, as necessary. 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 for this position is $100,000 - $125,000 annually. 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 recruiting@quidelortho.com. #LI-HF1