Automation Process Engineer

Posted 3 Days Ago
Be an Early Applicant
Pompano Beach, FL
68K-116K Annually
Junior
Healthtech • Biotech
The Role
The Automation Engineer will lead manufacturing automated system installation projects, define and maintain process equipment systems, troubleshoot software issues, and drive continuous improvement programs to enhance operational efficiency while ensuring compliance with quality and regulatory standards.
Summary Generated by Built In

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

The Automation Process Engineer will play a key role in designing, implementing, and optimizing automated systems and processes in a medical device manufacturing or production environment. A strong foundation in industrial automation, control systems, process engineering, and technology-driven improvements is essential. This role involves close collaboration with cross-functional teams to enhance efficiency, reduce costs, improve product quality, and drive overall production performance. Experience with medical device technologies in an FDA-regulated environment is highly relevant to this position.

Location: This position is based onsite in Pompano Beach, FL.

The Responsibilities

  • Evaluate and analyze current manufacturing processes, recommending automation enhancements to boost efficiency, throughput, and cost savings.

  • Lead automation projects from conception to execution, including budget management, scheduling, resource allocation, and adherence to safety regulations.

  • Develop and program PLC (Programmable Logic Controller) and SCADA (Supervisory Control and Data Acquisition) systems to control and monitor production processes.

  • Troubleshoot and resolve issues with automated equipment and processes to minimize downtime and ensure consistent production flow.

  • Monitor and analyze process data to assess the efficiency of automation systems, identifying areas for improvement.

  • Collaborate with production, quality, and maintenance teams to implement integrated solutions that enhance process performance.

  • Provide operational support for manufacturing lines, including root cause investigations, change control documentation, and validation processes to meet business and compliance standards.

  • Review, assess, and incorporate new, compliant technologies to benefit the business.

The Individual

Required

  • Bachelor's degree in Mechanical, Electrical, or Industrial Engineering (or related field).

  • 3-5 years of experience in automation engineering or process engineering within a manufacturing setting.

  • In-depth knowledge of PLCs, SCADA, and other industrial control systems.

  • Proficiency in programming languages such as Ladder Logic or other relevant automation tools.

  • Experience with electronic hardware, robotics, sensor integration, and HMI (Human-Machine Interface) systems.

  • Familiarity with Lean Manufacturing, Six Sigma, or other continuous improvement methodologies.

  • Strong analytical, problem-solving, and troubleshooting skills.

  • Excellent communication and teamwork skills.

  • Ability to travel up to 5%.

Preferred

  • Certification in automation or process control.

  • Experience with Industry 4.0 technologies, such as IoT, AI, and data analytics.

Interactions:

Internal

Collaboration with various internal departments and teams.

External

Liaison with vendors

Work Environment:

The work environment characteristics are representative of an office, laboratory and manufacturing environment. Flexible work hours to meet project deadlines. May work with hazardous materials.

Physical Demands:

Position requires ability to lift up to 30 lbs., work within restricted areas confined by equipment. Up to 50% of time/work within a low humidity environment with potential exposure to biological, toxic and corrosive reagents; and up to 50% is required to work within the confinements of a cubical style office, and also within a laboratory setting. Walking, standing and sitting for longs periods of time are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Must be willing to work 1st or 2nd shift. Position requires use of Personal Protective Equipment as posted.

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 $68,000 - $116,000. 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 [email protected].

#LI-HF1


 

Top Skills

Delphi
Rockwell
SQL
The Company
HQ: Raritan, NJ
4,457 Employees
On-site Workplace

What We Do

Ortho Clinical Diagnostics (Nasdaq: OCDX) is one of the world’s largest pure-play in vitro diagnostics (IVD) companies dedicated to transforming patient care.

More than 800,000 patients across the world are impacted by Ortho’s tests each day. Because Every Test is a Life, Ortho provides hospitals, hospital networks, clinical laboratories and blood banks around the world with innovative technology and tools to ensure test results are fast, accurate, and reliable. Ortho's customized solutions enhance clinical outcomes, improve efficiency, overcome lab staffing challenges and reduce costs.

From launching the first product to determine Rh+ or Rh- blood type, developing the world’s first tests for the detection of antibodies against HIV and hepatitis C, introducing patented dry-slide technology and marketing the first U.S. Food and Drug Administration-authorized high-volume antibody and antigen tests for COVID-19, Ortho has been a pioneering leader in the IVD space for over 80 years.

The company is powered by Ortho Care, an award-winning, holistic service and support program that ensures best-in-class technical, field and remote service and inventory support to laboratories in more than 130 countries and territories around the globe.

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