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Master Scheduler Purchasing Lead

  • ... Rochester, New York, United States
  • ... Full time
  • ... Salary: 114000 per year
  • Posted on: Feb 29, 2024       Expires on: Apr 14, 2024

Master Scheduler Purchasing Lead   

JOB TITLE:

Master Scheduler Purchasing Lead

JOB TYPE:

Full-time

JOB LOCATION:

Rochester New York United States

JOB DESCRIPTION:

Full 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 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

As we continue to grow as one QuidelOrtho we are seeking a Master Scheduler/Purchasing Lead to support diagnostic consumables production in Rochester, NY.
The individual will ensure sufficient WW supply of products by developing optimized production and purchasing plans, monitoring plan execution, and coordinating changes as necessary.
As a key member of the production leadership team, he/she will provide day-to-day direction as well as strategic input for the site.

Primary day shift; may have to occasionally work off-shift or weekends to support production plans.

This position is in Rochester, NY.

The Responsibilities

  • Analyze demand, inventory, lead-times, and production capacity to develop production and purchasing plans to maximize output, minimize cost, and minimize backorders.
    Continuously monitors progress vs plans and adjusts as needed.

  • Leads a team of planning and purchasing professionals.
    Provides team leadership to foster employee growth and development.

  • Escalates product delivery gaps and leads discussions with WW Supply Chain team to proactively address backorder risks.

  • Coordinates priority setting with production leadership and shipping team members as needed.

  • Provides regular performance reports to management (ie: MPS, Inventory vs plan, etc.
    )

  • Comfortable performing ad-hoc analysis of production performance, demand, and inventory and provides recommendations to management.

  • Manages the Sales, Inventory, and Operations Planning (SIOP) reviews for the production site.

  • Accountable for raw material and WIP inventory plans.
    Individual will develop inventory projections, monitor progress to plan, report status to management, and adjust plans as required.

  • Oversees effective use of ERP tools and ensures master data integrity (BOMs, Routings, etc.
    ).

  • Identifies areas for improvement and takes initiative to implement improvements.

  • Interfaces with R&D and Engineering on new product introduction to the production site.

The Individual

Required:

  • Bachelors degree in Business, Supply Chain, Industrial Engineering, or related discipline required or equivalent combination of education and work experience may be considered.
    Advanced degree preferred.

  • Minimum of 6-8 years in relevant experience in supply chain, planning, manufacturing, or inventory management required.

  • Proven ability to prioritize and complete multiple tasks successfully.

  • Experience working with an inventory system (i.
    e.
    SAP, JDE, other) is required.

  • Experience working in a regulated manufacturing environment is highly preferred, (diagnostics, medical device, pharmaceutical).

  • Strong verbal and written communication skills required.

  • Strong influencing and negotiating skills required.

  • 10% domestic travel.

Preferred:

  • Previous experience managing people.

  • Advanced Excel skills.

  • Knowledge of current and applicable GMP and FDA regulations.

  • Experience working in a regulated manufacturing environment, (diagnostics, medical device, pharmaceutical).

The Key Working Relationships

Internal Partners: Manufacturing, Operations, Quality,

External Partners: Suppliers, Carriers

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

$71,000.
00 - 114,000.
00 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 recruiting@quidelortho.
com

#LI-AP1

Position Details

POSTED:

Feb 29, 2024

EMPLOYMENT:

Full-time

SALARY:

114000 per year

SNAPRECRUIT ID:

S-1709421358-442afb531ac16efdb07ecbf5a80e02e5

LOCATION:

New York United States

CITY:

Rochester

Job Origin:

jpick2

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Full 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 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

As we continue to grow as one QuidelOrtho we are seeking a Master Scheduler/Purchasing Lead to support diagnostic consumables production in Rochester, NY. The individual will ensure sufficient WW supply of products by developing optimized production and purchasing plans, monitoring plan execution, and coordinating changes as necessary. As a key member of the production leadership team, he/she will provide day-to-day direction as well as strategic input for the site.

Primary day shift; may have to occasionally work off-shift or weekends to support production plans.

This position is in Rochester, NY.

The Responsibilities

  • Analyze demand, inventory, lead-times, and production capacity to develop production and purchasing plans to maximize output, minimize cost, and minimize backorders. Continuously monitors progress vs plans and adjusts as needed.

  • Leads a team of planning and purchasing professionals. Provides team leadership to foster employee growth and development.

  • Escalates product delivery gaps and leads discussions with WW Supply Chain team to proactively address backorder risks.

  • Coordinates priority setting with production leadership and shipping team members as needed.

  • Provides regular performance reports to management (ie: MPS, Inventory vs plan, etc.)

  • Comfortable performing ad-hoc analysis of production performance, demand, and inventory and provides recommendations to management.

  • Manages the Sales, Inventory, and Operations Planning (SIOP) reviews for the production site.

  • Accountable for raw material and WIP inventory plans. Individual will develop inventory projections, monitor progress to plan, report status to management, and adjust plans as required.

  • Oversees effective use of ERP tools and ensures master data integrity (BOMs, Routings, etc.).

  • Identifies areas for improvement and takes initiative to implement improvements.

  • Interfaces with R&D and Engineering on new product introduction to the production site.

The Individual

Required:

  • Bachelors degree in Business, Supply Chain, Industrial Engineering, or related discipline required or equivalent combination of education and work experience may be considered. Advanced degree preferred.

  • Minimum of 6-8 years in relevant experience in supply chain, planning, manufacturing, or inventory management required.

  • Proven ability to prioritize and complete multiple tasks successfully.

  • Experience working with an inventory system (i.e. SAP, JDE, other) is required.

  • Experience working in a regulated manufacturing environment is highly preferred, (diagnostics, medical device, pharmaceutical).

  • Strong verbal and written communication skills required.

  • Strong influencing and negotiating skills required.

  • 10% domestic travel.

Preferred:

  • Previous experience managing people.

  • Advanced Excel skills.

  • Knowledge of current and applicable GMP and FDA regulations.

  • Experience working in a regulated manufacturing environment, (diagnostics, medical device, pharmaceutical).

The Key Working Relationships

Internal Partners: Manufacturing, Operations, Quality,

External Partners: Suppliers, Carriers

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

$71,000.00 - 114,000.00 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 recruiting@quidelortho.com

#LI-AP1

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