Manufacturing Operations Supervisor

2 days ago

Raritan, New Jersey, United States QuidelOrtho Full time
The Opportunity

QuidelOrtho, a world-leading in vitro diagnostics company, is seeking a Manufacturing Supervisor to join our team. As a key member of our Operations department, you will be responsible for providing supervision for the Fill/Label team, ensuring flawless execution against our Quality System to maintain regulatory compliance.

The ideal candidate will have a strong background in manufacturing, with a minimum of 5 years of experience and 3 years of experience as a manufacturing supervisor or similar leadership position. Proficiency in Microsoft Office and data entry software is required, as well as the ability to prioritize, lead, and/or support multiple projects at once.

Key Responsibilities:

  • Oversee day-to-day manufacturing schedule activities, including Fill/Label, and participate in cross-functional teams to identify areas for process improvement.
  • Actively manage development, performance assessments, and succession plans for direct reports, and coach and mentor employees to achieve goals and objectives.
  • Direct activities to ensure the manufacturing area remains in a state of compliance and inspection readiness, and ensure proper calibration and maintenance of equipment.
  • Complete on-time investigations of quality events and work with QA to ensure timely lot releases.
  • Achieve organization targets, including MPS attainment, scrap goals, MUV target, and productivity goal.

Requirements:

  • Associate degree with a minimum of 5 years of manufacturing experience.
  • Minimum of 3 years of experience as a manufacturing supervisor or similar leadership position.
  • Proficiency in Microsoft Office and data entry software.
  • Ability to prioritize, lead, and/or support multiple projects at once.

Preferred Qualifications:

  • Bachelor's degree in business, management, engineering, or a related field.
  • Knowledge of Quality Information Systems (SAP, Windchill (PLM), Customer/Failure Investigations, cGMP's).

Work Environment:

  • Must be mobile and able to independently transport themselves between various sites/locations.
  • 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.

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.

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