Patient Planning Manager, Cell Therapy in Devens, MA
Bristol-Myers Squibb
Patient Planning Manager, Cell Therapy in Devens, MA
Job Description
Responsibilities will include, but are not limited to the following: Product Planning & Production Scheduling Act as the point of contact for Supply chain and the finite Scheduling team Manage short term master production scheduling and manufacturing needs Manage and communicate patient schedule changes and impact to approved production plan Manage the in-coming flow following patient apheresis material; partner with Cell Therapy Material Operations, Manufacturing, & Quality to ensure readiness for prompt receipt, inspection, and start of processing Manage secondary packaging of final drug product and return shipment to patients Manage Site Supply Chain Standard Operating procedures Own and manage deviations and corrective/preventive actions Own and manage change controls Foster a culture of compliance and strong environmental, health, and safety performance Participate in and/or lead cross-functional teams to improve systems, processes, or internal/external performance 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. Preferred but not required: Certification in CPIM, CSCP, and/or CLTD Advanced proficiency in Site Scheduling / planning / ERP systems and analytics tools Advanced knowledge of fundamental concepts of materials management, planning, and site production scheduling Ability to effectively communicate problem statements and viable solution options using pro vs. con and cost vs. benefit approaches Ability to present data and analyses in an organized, clear, and concise manner Advanced proficiency in MS Office applications Excellent written and verbal communication skills Ability to work independently for extended periods of time Ability to work as a team and mentor peers and direct reports Ability to understand and solve complicated supply and demand problems Intermediate knowledge of cGMP/Pharmaceutical regulations Bachelor's degree required in Life Sciences, Supply Chain, or similar 5+ years relevant work experience required 3+ years of experience supporting ERP systems (preferably SAP). Experience in a Site Supply Chain Organization Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization Experience with lean six sigma projects and change execution management An equivalent combination of education, experience, and training may substitute.
Key Responsibilities
- Act as the point of contact for Supply chain and the finite Scheduling team
- Manage short term master production scheduling and manufacturing needs
- Manage and communicate patient schedule changes and impact to approved production plan
- Manage the in-coming flow following patient apheresis material
- Partner with Cell Therapy Material Operations, Manufacturing, & Quality to ensure readiness for prompt receipt, inspection, and start of processing
- Manage secondary packaging of final drug product and return shipment to patients
- Manage Site Supply Chain Standard Operating procedures
- Own and manage deviations and corrective/preventive actions
- Own and manage change controls
- Foster a culture of compliance and strong environmental, health, and safety performance
- Participate in and/or lead cross-functional teams to improve systems, processes, or internal/external performance
Required Qualifications
- Bachelor's degree in Life Sciences, Supply Chain, or similar
- + years relevant work experience
- Intermediate knowledge of cGMP/Pharmaceutical regulations
Preferred Qualifications
- Certification in CPIM, CSCP, and/or CLTD
- Advanced proficiency in Site Scheduling / planning / ERP systems and analytics tools
- Advanced knowledge of fundamental concepts of materials management, planning, and site production scheduling
- + years of experience supporting ERP systems (preferably SAP)
- Experience in a Site Supply Chain Organization
- Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization
- Experience with lean six sigma projects and change execution management
Skills Required
- Ability to effectively communicate problem statements and viable solution options using pro vs. con and cost vs. benefit approaches
- Ability to present data and analyses in an organized, clear, and concise manner
- Advanced proficiency in MS Office applications
- Excellent written and verbal communication skills
- Ability to work independently for extended periods of time
- Ability to work as a team and mentor peers and direct reports
- Ability to understand and solve complicated supply and demand problems
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
- Devens MA, United States
Salary
Estimated Salary Rangemedium confidence
120,000 - 180,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to effectively communicate problem statements and viable solution options using pro vs. con and cost vs. benefit approachesintermediate
- Ability to present data and analyses in an organized, clear, and concise mannerintermediate
- Advanced proficiency in MS Office applicationsintermediate
- Excellent written and verbal communication skillsintermediate
- Ability to work independently for extended periods of timeintermediate
- Ability to work as a team and mentor peers and direct reportsintermediate
- Ability to understand and solve complicated supply and demand problemsintermediate
Required Qualifications
- Bachelor's degree in Life Sciences, Supply Chain, or similar (experience)
- + years relevant work experience (experience)
- Intermediate knowledge of cGMP/Pharmaceutical regulations (experience)
Preferred Qualifications
- Certification in CPIM, CSCP, and/or CLTD (experience)
- Advanced proficiency in Site Scheduling / planning / ERP systems and analytics tools (experience)
- Advanced knowledge of fundamental concepts of materials management, planning, and site production scheduling (experience)
- + years of experience supporting ERP systems (preferably SAP) (experience)
- Experience in a Site Supply Chain Organization (experience)
- Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization (experience)
- Experience with lean six sigma projects and change execution management (experience)
Responsibilities
- Act as the point of contact for Supply chain and the finite Scheduling team
- Manage short term master production scheduling and manufacturing needs
- Manage and communicate patient schedule changes and impact to approved production plan
- Manage the in-coming flow following patient apheresis material
- Partner with Cell Therapy Material Operations, Manufacturing, & Quality to ensure readiness for prompt receipt, inspection, and start of processing
- Manage secondary packaging of final drug product and return shipment to patients
- Manage Site Supply Chain Standard Operating procedures
- Own and manage deviations and corrective/preventive actions
- Own and manage change controls
- Foster a culture of compliance and strong environmental, health, and safety performance
- Participate in and/or lead cross-functional teams to improve systems, processes, or internal/external performance
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
Answer 10 quick questions to check your fit for Patient Planning Manager, Cell Therapy in Devens, MA @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs
Patient Planning Manager, Cell Therapy in Devens, MA
Bristol-Myers Squibb
Patient Planning Manager, Cell Therapy in Devens, MA
Job Description
Responsibilities will include, but are not limited to the following: Product Planning & Production Scheduling Act as the point of contact for Supply chain and the finite Scheduling team Manage short term master production scheduling and manufacturing needs Manage and communicate patient schedule changes and impact to approved production plan Manage the in-coming flow following patient apheresis material; partner with Cell Therapy Material Operations, Manufacturing, & Quality to ensure readiness for prompt receipt, inspection, and start of processing Manage secondary packaging of final drug product and return shipment to patients Manage Site Supply Chain Standard Operating procedures Own and manage deviations and corrective/preventive actions Own and manage change controls Foster a culture of compliance and strong environmental, health, and safety performance Participate in and/or lead cross-functional teams to improve systems, processes, or internal/external performance 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. Preferred but not required: Certification in CPIM, CSCP, and/or CLTD Advanced proficiency in Site Scheduling / planning / ERP systems and analytics tools Advanced knowledge of fundamental concepts of materials management, planning, and site production scheduling Ability to effectively communicate problem statements and viable solution options using pro vs. con and cost vs. benefit approaches Ability to present data and analyses in an organized, clear, and concise manner Advanced proficiency in MS Office applications Excellent written and verbal communication skills Ability to work independently for extended periods of time Ability to work as a team and mentor peers and direct reports Ability to understand and solve complicated supply and demand problems Intermediate knowledge of cGMP/Pharmaceutical regulations Bachelor's degree required in Life Sciences, Supply Chain, or similar 5+ years relevant work experience required 3+ years of experience supporting ERP systems (preferably SAP). Experience in a Site Supply Chain Organization Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization Experience with lean six sigma projects and change execution management An equivalent combination of education, experience, and training may substitute.
Key Responsibilities
- Act as the point of contact for Supply chain and the finite Scheduling team
- Manage short term master production scheduling and manufacturing needs
- Manage and communicate patient schedule changes and impact to approved production plan
- Manage the in-coming flow following patient apheresis material
- Partner with Cell Therapy Material Operations, Manufacturing, & Quality to ensure readiness for prompt receipt, inspection, and start of processing
- Manage secondary packaging of final drug product and return shipment to patients
- Manage Site Supply Chain Standard Operating procedures
- Own and manage deviations and corrective/preventive actions
- Own and manage change controls
- Foster a culture of compliance and strong environmental, health, and safety performance
- Participate in and/or lead cross-functional teams to improve systems, processes, or internal/external performance
Required Qualifications
- Bachelor's degree in Life Sciences, Supply Chain, or similar
- + years relevant work experience
- Intermediate knowledge of cGMP/Pharmaceutical regulations
Preferred Qualifications
- Certification in CPIM, CSCP, and/or CLTD
- Advanced proficiency in Site Scheduling / planning / ERP systems and analytics tools
- Advanced knowledge of fundamental concepts of materials management, planning, and site production scheduling
- + years of experience supporting ERP systems (preferably SAP)
- Experience in a Site Supply Chain Organization
- Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization
- Experience with lean six sigma projects and change execution management
Skills Required
- Ability to effectively communicate problem statements and viable solution options using pro vs. con and cost vs. benefit approaches
- Ability to present data and analyses in an organized, clear, and concise manner
- Advanced proficiency in MS Office applications
- Excellent written and verbal communication skills
- Ability to work independently for extended periods of time
- Ability to work as a team and mentor peers and direct reports
- Ability to understand and solve complicated supply and demand problems
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
- Devens MA, United States
Salary
Estimated Salary Rangemedium confidence
120,000 - 180,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to effectively communicate problem statements and viable solution options using pro vs. con and cost vs. benefit approachesintermediate
- Ability to present data and analyses in an organized, clear, and concise mannerintermediate
- Advanced proficiency in MS Office applicationsintermediate
- Excellent written and verbal communication skillsintermediate
- Ability to work independently for extended periods of timeintermediate
- Ability to work as a team and mentor peers and direct reportsintermediate
- Ability to understand and solve complicated supply and demand problemsintermediate
Required Qualifications
- Bachelor's degree in Life Sciences, Supply Chain, or similar (experience)
- + years relevant work experience (experience)
- Intermediate knowledge of cGMP/Pharmaceutical regulations (experience)
Preferred Qualifications
- Certification in CPIM, CSCP, and/or CLTD (experience)
- Advanced proficiency in Site Scheduling / planning / ERP systems and analytics tools (experience)
- Advanced knowledge of fundamental concepts of materials management, planning, and site production scheduling (experience)
- + years of experience supporting ERP systems (preferably SAP) (experience)
- Experience in a Site Supply Chain Organization (experience)
- Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization (experience)
- Experience with lean six sigma projects and change execution management (experience)
Responsibilities
- Act as the point of contact for Supply chain and the finite Scheduling team
- Manage short term master production scheduling and manufacturing needs
- Manage and communicate patient schedule changes and impact to approved production plan
- Manage the in-coming flow following patient apheresis material
- Partner with Cell Therapy Material Operations, Manufacturing, & Quality to ensure readiness for prompt receipt, inspection, and start of processing
- Manage secondary packaging of final drug product and return shipment to patients
- Manage Site Supply Chain Standard Operating procedures
- Own and manage deviations and corrective/preventive actions
- Own and manage change controls
- Foster a culture of compliance and strong environmental, health, and safety performance
- Participate in and/or lead cross-functional teams to improve systems, processes, or internal/external performance
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
Answer 10 quick questions to check your fit for Patient Planning Manager, Cell Therapy in Devens, MA @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs