Production Supervisor
Production Supervisor
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Job Description
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 6000 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 Production Supervisor for our Slides Manufacturing facility. This individual leads the Operations staff in a 24hr/day production environment to ensure business objectives are met. They do this by ensuring production work centers are fully staffed standard work is being followed standard times are being met and quality defects are being minimized. They will be expected to create a positive productive and accountable culture within their team. The Supervisor will also be expected to communicate and collaborate with support functions (Quality Materials Management etc.) across shifts as needed.
This position is in Rochester NY.
Schedule: Firemens Rotation: Two 12 hour days (6:00am-6:00pm) followed by two 12 hour nights (6:00pm-6:00am)
The Responsibilities
Lead and supervise the operations personnel and provide regular feedback on performance to KPIs and developing a cross trained team.
Accountable for the Crew adherence to Safety Quality and Compliance policies and when necessary counsel team members who are in violation of these policies. Adheres to policy and procedural guidelines.
Monitor and maintain adequate staffing levels to meet production targets.
Champion safety protocols and create a zero incident workplace through engagement of the team.
Drive continuous improvement using Lean principles OEE and structured problem solving
Identify opportunities for process enhancements and lead improvement projects that align with organizational goals
Performs other duties as assigned.
The Individual
Required:
High School Diploma or GED.
Proven experience in manufacturing supervision or a similar leadership role.
Proficiency in Microsoft Office (Excel Word PowerPoint) and an MRP system such as SAP or Oracle.
Strong commitment to SQDC metrics and operational excellence.
Proven leadership communication and problem-solving skills.
Ability to motivate coach and develop team members driving engagement and performance.
Knowledge of Continuous Improvement principles and methodologies 5S Lean manufacturing Structured Problem Solving
Preferred:
Prior Supervisory experience.
AAS/Bachelors degree in business related field
The Working Relationships
Internal Partners: Quality Engineers HR Safety Peer Supervisors Recruiting Production Planning
External Partners: Contract Staffing Agency
The Work Environment
The work environment characteristics are representative of a manufacturing laboratory and warehouse environment and include handling of viral and bacterial hazards potentially hazardous chemicals as well as infectious or potentially infectious bodily fluids tissues and samples. Up to 75% of the time you will be standing walking or sitting for extended periods of time. Ability to lift up to 50 lbs. Flexible work hours to meet project deadlines.
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 $65000 to $118000 and is bonus eligible. 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 r.
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Required Experience:
Manager
Employment Type
Full-Time
