Senior Manager, GMP Facilities
Bristol-Myers Squibb
Senior Manager, GMP Facilities
Job Description
Member of the Site Safety Committee. Champions safety and compliance as a leader within the Facilities & Engineering Department. Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products. Ensure that the right support structure is in place to facilitate compliance with those requirements. Supports the development of related procedures and programs, implement and monitor performance. Identifies areas of opportunity and prepares specific action plans to increase awareness and to maintain compliance. Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives. Communicate a clear vision for the team aligned with the Summit West and overall business objectives. Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment. Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output. Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues. In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications. Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability. Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards. Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services. Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe. Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities. Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical products. Develops relationships with diverse groups across the client base at the Summit West site. Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization. Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements Develops and monitors key performance indicators for utility operations. Drives appropriate actions to mitigate performance issues. 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 Experience managing the operations and maintenance of critical utilities supporting a manufacturing operation. Experience with Quality Management Systems, specifically Change Control. Experience interacting with regulatory agencies and local government officials. Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc. Specific knowledge of equipment reliability principles and processes as related to maintenance best practices. Knowledge and experience in supporting cell therapy processes. Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility. Working knowledge and experience with regulatory inspections preferably as an SME lead. Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilities. Experience leading a large team of multi-skilled trades within a regulated manufacturing environment. Experience managing OPEX and/or CAPEX budgets. Ability to manage or be an active team member of cross-functional project teams. Must have a BA degree in Facilities Management, Engineering, OR equivalent experience. Knowledge of BMS business objectives, strategies, and the pharmaceutical industry. Understanding of regulatory, environmental, GMP, GLP and OSHA regulations. Bachelor's degree in a technical field, preferably Engineering. An equivalent amount of education, certifications and experience to be considered. Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations. Minimum of 3 years' experience leading an Engineering and/or Facilities Team.
About the Role/Company
- The company operates within the pharmaceutical industry, specifically in cell therapy at the Summit West site
- The Facilities & Engineering Department is part of a larger organization focused on maintaining compliance and safety in pharmaceutical manufacturing
Key Responsibilities
- Champion safety and compliance as a leader within the Facilities & Engineering Department
- Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products
- Ensure that the right support structure is in place to facilitate compliance with those requirements
- Support the development of related procedures and programs, implement and monitor performance
- Identify areas of opportunity and prepare specific action plans to increase awareness and to maintain compliance
- Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives
- Communicate a clear vision for the team aligned with the Summit West and overall business objectives
- Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment
- Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output
- Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues
- In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications
- Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability
- Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards
- Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services
- Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe
- Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities
- Develops relationships with diverse groups across the client base at the Summit West site
- Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization
- Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements
- Develops and monitors key performance indicators for utility operations
- Drives appropriate actions to mitigate performance issues
Required Qualifications
- Bachelor's degree in a technical field, preferably Engineering
- Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations
- Minimum of 3 years' experience leading an Engineering and/or Facilities Team
- BA degree in Facilities Management, Engineering, OR equivalent experience
Preferred Qualifications
- Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc.
- Specific knowledge of equipment reliability principles and processes as related to maintenance best practices
- Knowledge and experience in supporting cell therapy processes
- Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility
- Working knowledge and experience with regulatory inspections preferably as an SME lead
- Experience managing OPEX and/or CAPEX budgets
Skills Required
- Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical products
- Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilities
- Experience managing the operations and maintenance of critical utilities supporting a manufacturing operation
- Experience with Quality Management Systems, specifically Change Control
- Experience interacting with regulatory agencies and local government officials
- Ability to manage or be an active team member of cross-functional project teams
- Knowledge of BMS business objectives, strategies, and the pharmaceutical industry
- Understanding of regulatory, environmental, GMP, GLP and OSHA regulations
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
Additional Requirements
- Member of the Site Safety Committee
Locations
- Summit West NJ, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
150,000 - 220,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical productsintermediate
- Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilitiesintermediate
- Experience managing the operations and maintenance of critical utilities supporting a manufacturing operationintermediate
- Experience with Quality Management Systems, specifically Change Controlintermediate
- Experience interacting with regulatory agencies and local government officialsintermediate
- Ability to manage or be an active team member of cross-functional project teamsintermediate
- Knowledge of BMS business objectives, strategies, and the pharmaceutical industryintermediate
- Understanding of regulatory, environmental, GMP, GLP and OSHA regulationsintermediate
Required Qualifications
- Bachelor's degree in a technical field, preferably Engineering (experience)
- Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations (experience)
- Minimum of 3 years' experience leading an Engineering and/or Facilities Team (experience)
- BA degree in Facilities Management, Engineering, OR equivalent experience (experience)
Preferred Qualifications
- Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc. (experience)
- Specific knowledge of equipment reliability principles and processes as related to maintenance best practices (experience)
- Knowledge and experience in supporting cell therapy processes (experience)
- Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility (experience)
- Working knowledge and experience with regulatory inspections preferably as an SME lead (experience)
- Experience managing OPEX and/or CAPEX budgets (experience)
Responsibilities
- Champion safety and compliance as a leader within the Facilities & Engineering Department
- Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products
- Ensure that the right support structure is in place to facilitate compliance with those requirements
- Support the development of related procedures and programs, implement and monitor performance
- Identify areas of opportunity and prepare specific action plans to increase awareness and to maintain compliance
- Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives
- Communicate a clear vision for the team aligned with the Summit West and overall business objectives
- Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment
- Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output
- Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues
- In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications
- Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability
- Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards
- Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services
- Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe
- Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities
- Develops relationships with diverse groups across the client base at the Summit West site
- Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization
- Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements
- Develops and monitors key performance indicators for utility operations
- Drives appropriate actions to mitigate performance issues
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
Senior Manager, GMP Facilities
Bristol-Myers Squibb
Senior Manager, GMP Facilities
Job Description
Member of the Site Safety Committee. Champions safety and compliance as a leader within the Facilities & Engineering Department. Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products. Ensure that the right support structure is in place to facilitate compliance with those requirements. Supports the development of related procedures and programs, implement and monitor performance. Identifies areas of opportunity and prepares specific action plans to increase awareness and to maintain compliance. Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives. Communicate a clear vision for the team aligned with the Summit West and overall business objectives. Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment. Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output. Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues. In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications. Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability. Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards. Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services. Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe. Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities. Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical products. Develops relationships with diverse groups across the client base at the Summit West site. Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization. Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements Develops and monitors key performance indicators for utility operations. Drives appropriate actions to mitigate performance issues. 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 Experience managing the operations and maintenance of critical utilities supporting a manufacturing operation. Experience with Quality Management Systems, specifically Change Control. Experience interacting with regulatory agencies and local government officials. Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc. Specific knowledge of equipment reliability principles and processes as related to maintenance best practices. Knowledge and experience in supporting cell therapy processes. Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility. Working knowledge and experience with regulatory inspections preferably as an SME lead. Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilities. Experience leading a large team of multi-skilled trades within a regulated manufacturing environment. Experience managing OPEX and/or CAPEX budgets. Ability to manage or be an active team member of cross-functional project teams. Must have a BA degree in Facilities Management, Engineering, OR equivalent experience. Knowledge of BMS business objectives, strategies, and the pharmaceutical industry. Understanding of regulatory, environmental, GMP, GLP and OSHA regulations. Bachelor's degree in a technical field, preferably Engineering. An equivalent amount of education, certifications and experience to be considered. Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations. Minimum of 3 years' experience leading an Engineering and/or Facilities Team.
About the Role/Company
- The company operates within the pharmaceutical industry, specifically in cell therapy at the Summit West site
- The Facilities & Engineering Department is part of a larger organization focused on maintaining compliance and safety in pharmaceutical manufacturing
Key Responsibilities
- Champion safety and compliance as a leader within the Facilities & Engineering Department
- Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products
- Ensure that the right support structure is in place to facilitate compliance with those requirements
- Support the development of related procedures and programs, implement and monitor performance
- Identify areas of opportunity and prepare specific action plans to increase awareness and to maintain compliance
- Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives
- Communicate a clear vision for the team aligned with the Summit West and overall business objectives
- Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment
- Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output
- Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues
- In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications
- Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability
- Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards
- Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services
- Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe
- Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities
- Develops relationships with diverse groups across the client base at the Summit West site
- Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization
- Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements
- Develops and monitors key performance indicators for utility operations
- Drives appropriate actions to mitigate performance issues
Required Qualifications
- Bachelor's degree in a technical field, preferably Engineering
- Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations
- Minimum of 3 years' experience leading an Engineering and/or Facilities Team
- BA degree in Facilities Management, Engineering, OR equivalent experience
Preferred Qualifications
- Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc.
- Specific knowledge of equipment reliability principles and processes as related to maintenance best practices
- Knowledge and experience in supporting cell therapy processes
- Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility
- Working knowledge and experience with regulatory inspections preferably as an SME lead
- Experience managing OPEX and/or CAPEX budgets
Skills Required
- Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical products
- Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilities
- Experience managing the operations and maintenance of critical utilities supporting a manufacturing operation
- Experience with Quality Management Systems, specifically Change Control
- Experience interacting with regulatory agencies and local government officials
- Ability to manage or be an active team member of cross-functional project teams
- Knowledge of BMS business objectives, strategies, and the pharmaceutical industry
- Understanding of regulatory, environmental, GMP, GLP and OSHA regulations
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
Additional Requirements
- Member of the Site Safety Committee
Locations
- Summit West NJ, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
150,000 - 220,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical productsintermediate
- Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilitiesintermediate
- Experience managing the operations and maintenance of critical utilities supporting a manufacturing operationintermediate
- Experience with Quality Management Systems, specifically Change Controlintermediate
- Experience interacting with regulatory agencies and local government officialsintermediate
- Ability to manage or be an active team member of cross-functional project teamsintermediate
- Knowledge of BMS business objectives, strategies, and the pharmaceutical industryintermediate
- Understanding of regulatory, environmental, GMP, GLP and OSHA regulationsintermediate
Required Qualifications
- Bachelor's degree in a technical field, preferably Engineering (experience)
- Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations (experience)
- Minimum of 3 years' experience leading an Engineering and/or Facilities Team (experience)
- BA degree in Facilities Management, Engineering, OR equivalent experience (experience)
Preferred Qualifications
- Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc. (experience)
- Specific knowledge of equipment reliability principles and processes as related to maintenance best practices (experience)
- Knowledge and experience in supporting cell therapy processes (experience)
- Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility (experience)
- Working knowledge and experience with regulatory inspections preferably as an SME lead (experience)
- Experience managing OPEX and/or CAPEX budgets (experience)
Responsibilities
- Champion safety and compliance as a leader within the Facilities & Engineering Department
- Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products
- Ensure that the right support structure is in place to facilitate compliance with those requirements
- Support the development of related procedures and programs, implement and monitor performance
- Identify areas of opportunity and prepare specific action plans to increase awareness and to maintain compliance
- Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives
- Communicate a clear vision for the team aligned with the Summit West and overall business objectives
- Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment
- Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output
- Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues
- In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications
- Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability
- Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards
- Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services
- Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe
- Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities
- Develops relationships with diverse groups across the client base at the Summit West site
- Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization
- Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements
- Develops and monitors key performance indicators for utility operations
- Drives appropriate actions to mitigate performance issues
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