Associate Operator

Description:

Quidel Ortho, formed by the merger of Quidel Corporation and Ortho Clinical Diagnostics, is a global leader in in vitro diagnostics, delivering reliable and accurate testing solutions across more than 130 countries. With over 6,000 employees worldwide, the company focuses on advancing immunoassay, molecular testing, clinical chemistry, and transfusion medicine to support patient care in hospitals, clinics, labs, and at home.

The Associate Operator role in the Slide Assembly Department is a key position responsible for maintaining production quality and compliance with company policies, procedures, and regulatory standards. The role demands strong adherence to Environmental Health & Safety (EHS) practices and Good Manufacturing Practices (GMP). The position operates on a “Firemen’s Rotation” schedule: two 12-hour day shifts (6:00am–6:00pm) followed by two 12-hour night shifts (6:00pm–6:00am).

Key Responsibilities:

• Operate and meet production metrics on automated production machines with minimal supervision.

• Assist in troubleshooting and basic repairs of equipment.

• Perform data entry in systems such as SAP and SPIDER.

• Conduct basic quality checks and escalate issues when necessary.

• Participate in simple root cause analyses using tools like 5 Whys and Fishbone Diagram.

• Follow and update SOPs, work instructions, and job plans.

• Perform basic machine adjustments under senior operator guidance.

• Support effective communication and foster positive workplace relationships.

• Flexibly perform multiple functions across the Work Center as required.

• Identify EH&S opportunities and participate in implementing solutions.

• Contribute to cross-training initiatives and continuous improvement activities.

Required Skills & Qualifications:

• High School Diploma, GED, or equivalent education/work experience.

• 1–3 years of experience in automated production or related systems.

• Ability to work effectively in a team.

• Basic safety knowledge and application in manufacturing tasks.

• Familiarity with GMP practices in regulated industries.

• Ability to handle multiple pieces of automated equipment.

• Basic problem-solving and documentation accuracy skills.

Additional Skills:

• Intermediate math and communication skills.

• Knowledge of tools, 6S principles, and HMI screen navigation.

• Ability to recognize failure patterns in automated lines.

• Strong accuracy in completing documentation following good practices.

Work Environment:
The role involves working in a manufacturing or laboratory setting with exposure to viral/bacterial hazards, chemicals, and potentially infectious samples. Physical requirements include standing, walking, or sitting for extended periods (up to 75% of the time) and lifting up to 50 lbs. Flexibility in working hours is expected to meet project demands.

Compensation & Benefits:
The hourly pay range is $18.12 – $23.38, with final compensation determined by factors such as skills, experience, and education. QuidelOrtho offers a comprehensive benefits package, including medical, dental, vision, life, and disability insurance, a 401(k) plan, Employee Stock Purchase Plan, paid time off, sick leave, and paid holidays.

Equal Opportunity Commitment:
QuidelOrtho is an equal opportunity employer committed to diversity and inclusion, ensuring that all qualified applicants receive consideration without discrimination. Reasonable accommodations are available for individuals with disabilities throughout the application process.