Associate Specialist Production Planning
Bristol-Myers Squibb
Associate Specialist Production Planning
Job Description
Provides manufacturing operations with a plan that maximizes efficiency, resources, and capacity. Work on projects/matters of moderate complexity. Evaluates and develops scheduling tools and provides technical expertise Plans and schedules production schedules to meet product demand at the site. Plan and schedule all associated production and support activities including intermediates, product shipment, facility and equipment maintenance. Work with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing. Build strong relationships and communication with all functions. Provide exceptional customer service. Knowledge of forecasting, capacity planning, and production planning. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturing. Ability to work independently on projects or problems of moderate scope to meet objectives. Troubleshoots and identifies causes and suggests solutions. Attention to detail and ability to perform with a high degree of accuracy. Source of imaginative, thorough, and innovative solutions to a wide range of difficult problems. Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping preferred. Supports an environment that encourages continuous improvement, best practices and appropriate risk taking. Ability to influence key stakeholders of internal and external teams. Excellent communication and presentation skills as well as the ability to effectively communicate across all levels of the company. Strong analytical and problem-solving abilities. Expert in Microsoft Office programs. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities 0-3 years preferred; 1+ years of scheduling experience in cGMP manufacturing environment desired. HS Diploma. Experience in scheduling cell therapy manufacturing preferred. Experience in material planning and/or finite scheduling in a medium to high volume environment, knowledge of scheduling platforms preferred.
Key Responsibilities
- Provide manufacturing operations with a plan that maximizes efficiency, resources, and capacity
- Work on projects/matters of moderate complexity
- Evaluate and develop scheduling tools
- Provide technical expertise
- Plan and schedule production schedules to meet product demand at the site
- Plan and schedule all associated production and support activities including intermediates, product shipment, facility and equipment maintenance
- Work with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing
- Build strong relationships and communication with all functions
- Provide exceptional customer service
- Troubleshoot and identify causes and suggest solutions
- Support an environment that encourages continuous improvement, best practices and appropriate risk taking
Required Qualifications
- High School Diploma
- -3 years of experience preferred
- + years of scheduling experience in cGMP manufacturing environment desired
Preferred Qualifications
- Experience in scheduling cell therapy manufacturing
- Experience in material planning and/or finite scheduling in a medium to high volume environment
- Knowledge of scheduling platforms
- Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping
Skills Required
- Knowledge of forecasting, capacity planning, and production planning
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturing
- Ability to work independently on projects or problems of moderate scope to meet objectives
- Attention to detail and ability to perform with a high degree of accuracy
- Source of imaginative, thorough, and innovative solutions to a wide range of difficult problems
- Ability to influence key stakeholders of internal and external teams
- Excellent communication and presentation skills
- Ability to effectively communicate across all levels of the company
- Strong analytical and problem-solving abilities
- Expert in Microsoft Office programs
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
Locations
- Bothell WA, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
60,000 - 90,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Knowledge of forecasting, capacity planning, and production planningintermediate
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturingintermediate
- Ability to work independently on projects or problems of moderate scope to meet objectivesintermediate
- Attention to detail and ability to perform with a high degree of accuracyintermediate
- Source of imaginative, thorough, and innovative solutions to a wide range of difficult problemsintermediate
- Ability to influence key stakeholders of internal and external teamsintermediate
- Excellent communication and presentation skillsintermediate
- Ability to effectively communicate across all levels of the companyintermediate
- Strong analytical and problem-solving abilitiesintermediate
- Expert in Microsoft Office programsintermediate
Required Qualifications
- High School Diploma (experience)
- -3 years of experience preferred (experience)
- + years of scheduling experience in cGMP manufacturing environment desired (experience)
Preferred Qualifications
- Experience in scheduling cell therapy manufacturing (experience)
- Experience in material planning and/or finite scheduling in a medium to high volume environment (experience)
- Knowledge of scheduling platforms (experience)
- Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping (experience)
Responsibilities
- Provide manufacturing operations with a plan that maximizes efficiency, resources, and capacity
- Work on projects/matters of moderate complexity
- Evaluate and develop scheduling tools
- Provide technical expertise
- Plan and schedule production schedules to meet product demand at the site
- Plan and schedule all associated production and support activities including intermediates, product shipment, facility and equipment maintenance
- Work with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing
- Build strong relationships and communication with all functions
- Provide exceptional customer service
- Troubleshoot and identify causes and suggest solutions
- Support an environment that encourages continuous improvement, best practices and appropriate risk taking
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
Tags & Categories
Associate Specialist Production Planning
Bristol-Myers Squibb
Associate Specialist Production Planning
Job Description
Provides manufacturing operations with a plan that maximizes efficiency, resources, and capacity. Work on projects/matters of moderate complexity. Evaluates and develops scheduling tools and provides technical expertise Plans and schedules production schedules to meet product demand at the site. Plan and schedule all associated production and support activities including intermediates, product shipment, facility and equipment maintenance. Work with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing. Build strong relationships and communication with all functions. Provide exceptional customer service. Knowledge of forecasting, capacity planning, and production planning. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturing. Ability to work independently on projects or problems of moderate scope to meet objectives. Troubleshoots and identifies causes and suggests solutions. Attention to detail and ability to perform with a high degree of accuracy. Source of imaginative, thorough, and innovative solutions to a wide range of difficult problems. Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping preferred. Supports an environment that encourages continuous improvement, best practices and appropriate risk taking. Ability to influence key stakeholders of internal and external teams. Excellent communication and presentation skills as well as the ability to effectively communicate across all levels of the company. Strong analytical and problem-solving abilities. Expert in Microsoft Office programs. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities 0-3 years preferred; 1+ years of scheduling experience in cGMP manufacturing environment desired. HS Diploma. Experience in scheduling cell therapy manufacturing preferred. Experience in material planning and/or finite scheduling in a medium to high volume environment, knowledge of scheduling platforms preferred.
Key Responsibilities
- Provide manufacturing operations with a plan that maximizes efficiency, resources, and capacity
- Work on projects/matters of moderate complexity
- Evaluate and develop scheduling tools
- Provide technical expertise
- Plan and schedule production schedules to meet product demand at the site
- Plan and schedule all associated production and support activities including intermediates, product shipment, facility and equipment maintenance
- Work with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing
- Build strong relationships and communication with all functions
- Provide exceptional customer service
- Troubleshoot and identify causes and suggest solutions
- Support an environment that encourages continuous improvement, best practices and appropriate risk taking
Required Qualifications
- High School Diploma
- -3 years of experience preferred
- + years of scheduling experience in cGMP manufacturing environment desired
Preferred Qualifications
- Experience in scheduling cell therapy manufacturing
- Experience in material planning and/or finite scheduling in a medium to high volume environment
- Knowledge of scheduling platforms
- Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping
Skills Required
- Knowledge of forecasting, capacity planning, and production planning
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturing
- Ability to work independently on projects or problems of moderate scope to meet objectives
- Attention to detail and ability to perform with a high degree of accuracy
- Source of imaginative, thorough, and innovative solutions to a wide range of difficult problems
- Ability to influence key stakeholders of internal and external teams
- Excellent communication and presentation skills
- Ability to effectively communicate across all levels of the company
- Strong analytical and problem-solving abilities
- Expert in Microsoft Office programs
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
Locations
- Bothell WA, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
60,000 - 90,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Knowledge of forecasting, capacity planning, and production planningintermediate
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturingintermediate
- Ability to work independently on projects or problems of moderate scope to meet objectivesintermediate
- Attention to detail and ability to perform with a high degree of accuracyintermediate
- Source of imaginative, thorough, and innovative solutions to a wide range of difficult problemsintermediate
- Ability to influence key stakeholders of internal and external teamsintermediate
- Excellent communication and presentation skillsintermediate
- Ability to effectively communicate across all levels of the companyintermediate
- Strong analytical and problem-solving abilitiesintermediate
- Expert in Microsoft Office programsintermediate
Required Qualifications
- High School Diploma (experience)
- -3 years of experience preferred (experience)
- + years of scheduling experience in cGMP manufacturing environment desired (experience)
Preferred Qualifications
- Experience in scheduling cell therapy manufacturing (experience)
- Experience in material planning and/or finite scheduling in a medium to high volume environment (experience)
- Knowledge of scheduling platforms (experience)
- Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping (experience)
Responsibilities
- Provide manufacturing operations with a plan that maximizes efficiency, resources, and capacity
- Work on projects/matters of moderate complexity
- Evaluate and develop scheduling tools
- Provide technical expertise
- Plan and schedule production schedules to meet product demand at the site
- Plan and schedule all associated production and support activities including intermediates, product shipment, facility and equipment maintenance
- Work with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing
- Build strong relationships and communication with all functions
- Provide exceptional customer service
- Troubleshoot and identify causes and suggest solutions
- Support an environment that encourages continuous improvement, best practices and appropriate risk taking
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
Tags & Categories