Manufacturing Supervisor

1 week ago

Raritan, New Jersey, United States Ortho Clinical Diagnostics Full time
Manufacturing Supervisor Opportunity

At Ortho Clinical Diagnostics, we are seeking a skilled Manufacturing Supervisor to join our team. This role will be responsible for overseeing the Fill/Label team and ensuring flawless execution against our Quality System to maintain regulatory compliance.

Key Responsibilities:
  • Supervise Filling and Labeling operators to ensure production schedules are met and quality standards are maintained.
  • Develop short-term tactical goals and objectives, as well as longer-term strategies to drive efficiencies and continuous improvement in manufacturing quality and compliance performance.
  • Collaborate with the Quality Team to identify and standardize best practices, drive efficiency and compliance excellence, and enforce cGMPs and EHS requirements.
  • Manage development, performance assessments, and succession plans for direct reports, and provide coaching and mentoring to achieve goals and objectives.
  • Review documentation of training for completeness and content, and promote cGMPs, proper safety practices, and proper environmental practices.
  • Make hiring and termination decisions, and complete performance appraisals of manufacturing team members.
  • Direct activities to ensure the manufacturing area is in a continued state of compliance and inspection readiness.
  • Ensure proper calibration and maintenance of equipment, and document completion correctly.
  • Complete on-time investigation 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.
  • Identify possible manufacturing constraints and improvement opportunities, and actively participate in Manufacturing daily meetings with cross-functional teams.
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, delegate tasks, and demonstrate effective oral and written communication skills.
  • Strong interpersonal skills, problem-solving skills, and ability to work in a cGMP area and/or clean room environment.
Work Environment:

The Manufacturing Supervisor will be required to work in a fast-paced manufacturing environment, frequently communicating with coworkers, and occasionally working other shifts. The position requires the ability to lift up to 40 lbs, work with blood, blood products, and chemicals, and pass a vision acuity test for inspection of work in process and finished goods.

QuidelOrtho is an equal opportunity employer and is committed to ensuring all individuals have an opportunity to apply for positions 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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