Training Specialist, Cell Therapy Manufacturing in Devens, MA
Bristol-Myers Squibb
Training Specialist, Cell Therapy Manufacturing in Devens, MA
Job Description
Demonstrates the ability to execute operations as described in standard operating procedures and batch records. Demonstrates strong practical and theoretical knowledge in their work. Completes documentation required by training policies and standard operating procedures. Performs and demonstrates tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Qualifies new employees on assigned curriculum required of their job functions. Executes trainee requalification's as needed. On-time completion of training assignments to ensure technical skills and knowledge are adequate prior to the training of other individuals. Collaborates with support groups on recommendations and solving training gaps between new hire on boarding and the transition to manufacturing operations. Identifies innovative solutions. Supports creation of manufacturing training materials such as On-The-Job-Trainings and Instructor-Led-Trainings. Works independently and escalates issues appropriately, works with Management to resolve. 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. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing preferred. Must be able to gown into a cleanroom environment. Must be able to be near strong magnets. Experience with delivering training to adult learners and groups. Experience and knowledge of Cell Therapy operations preferred. Communicates effectively between peers, trainees, and cross-functional stakeholders. Ability to work collaboratively with all employees at all levels. Demonstrates strong problem solving and critical thinking skills. 4+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience Bachelors in relevant science or engineering discipline, or equivalent in work experience.
Key Responsibilities
- Execute operations as described in standard operating procedures and batch records
- Complete documentation required by training policies and standard operating procedures
- Perform and demonstrate tasks in a manner consistent with safety policies, quality systems, and GMP requirements
- Qualify new employees on assigned curriculum required of their job functions
- Execute trainee requalifications as needed
- Ensure on-time completion of training assignments to ensure technical skills and knowledge are adequate prior to training others
- Collaborate with support groups on recommendations and solving training gaps between new hire onboarding and the transition to manufacturing operations
- Identify innovative solutions
- Support creation of manufacturing training materials such as On-The-Job-Trainings and Instructor-Led-Trainings
- Work independently and escalate issues appropriately, work with Management to resolve
Required Qualifications
- + years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience
- Bachelors in relevant science or engineering discipline, or equivalent in work experience
Preferred Qualifications
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing
- Experience and knowledge of Cell Therapy operations
Skills Required
- Strong practical and theoretical knowledge in their work
- Ability to gown into a cleanroom environment
- Ability to be near strong magnets
- Experience with delivering training to adult learners and groups
- Effective communication between peers, trainees, and cross-functional stakeholders
- Ability to work collaboratively with all employees at all levels
- Strong problem solving and critical thinking skills
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
80,000 - 120,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Strong practical and theoretical knowledge in their workintermediate
- Ability to gown into a cleanroom environmentintermediate
- Ability to be near strong magnetsintermediate
- Experience with delivering training to adult learners and groupsintermediate
- Effective communication between peers, trainees, and cross-functional stakeholdersintermediate
- Ability to work collaboratively with all employees at all levelsintermediate
- Strong problem solving and critical thinking skillsintermediate
Required Qualifications
- + years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience (experience)
- Bachelors in relevant science or engineering discipline, or equivalent in work experience (experience)
Preferred Qualifications
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing (experience)
- Experience and knowledge of Cell Therapy operations (experience)
Responsibilities
- Execute operations as described in standard operating procedures and batch records
- Complete documentation required by training policies and standard operating procedures
- Perform and demonstrate tasks in a manner consistent with safety policies, quality systems, and GMP requirements
- Qualify new employees on assigned curriculum required of their job functions
- Execute trainee requalifications as needed
- Ensure on-time completion of training assignments to ensure technical skills and knowledge are adequate prior to training others
- Collaborate with support groups on recommendations and solving training gaps between new hire onboarding and the transition to manufacturing operations
- Identify innovative solutions
- Support creation of manufacturing training materials such as On-The-Job-Trainings and Instructor-Led-Trainings
- Work independently and escalate issues appropriately, work with Management to resolve
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
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Training Specialist, Cell Therapy Manufacturing in Devens, MA
Bristol-Myers Squibb
Training Specialist, Cell Therapy Manufacturing in Devens, MA
Job Description
Demonstrates the ability to execute operations as described in standard operating procedures and batch records. Demonstrates strong practical and theoretical knowledge in their work. Completes documentation required by training policies and standard operating procedures. Performs and demonstrates tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Qualifies new employees on assigned curriculum required of their job functions. Executes trainee requalification's as needed. On-time completion of training assignments to ensure technical skills and knowledge are adequate prior to the training of other individuals. Collaborates with support groups on recommendations and solving training gaps between new hire on boarding and the transition to manufacturing operations. Identifies innovative solutions. Supports creation of manufacturing training materials such as On-The-Job-Trainings and Instructor-Led-Trainings. Works independently and escalates issues appropriately, works with Management to resolve. 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. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing preferred. Must be able to gown into a cleanroom environment. Must be able to be near strong magnets. Experience with delivering training to adult learners and groups. Experience and knowledge of Cell Therapy operations preferred. Communicates effectively between peers, trainees, and cross-functional stakeholders. Ability to work collaboratively with all employees at all levels. Demonstrates strong problem solving and critical thinking skills. 4+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience Bachelors in relevant science or engineering discipline, or equivalent in work experience.
Key Responsibilities
- Execute operations as described in standard operating procedures and batch records
- Complete documentation required by training policies and standard operating procedures
- Perform and demonstrate tasks in a manner consistent with safety policies, quality systems, and GMP requirements
- Qualify new employees on assigned curriculum required of their job functions
- Execute trainee requalifications as needed
- Ensure on-time completion of training assignments to ensure technical skills and knowledge are adequate prior to training others
- Collaborate with support groups on recommendations and solving training gaps between new hire onboarding and the transition to manufacturing operations
- Identify innovative solutions
- Support creation of manufacturing training materials such as On-The-Job-Trainings and Instructor-Led-Trainings
- Work independently and escalate issues appropriately, work with Management to resolve
Required Qualifications
- + years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience
- Bachelors in relevant science or engineering discipline, or equivalent in work experience
Preferred Qualifications
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing
- Experience and knowledge of Cell Therapy operations
Skills Required
- Strong practical and theoretical knowledge in their work
- Ability to gown into a cleanroom environment
- Ability to be near strong magnets
- Experience with delivering training to adult learners and groups
- Effective communication between peers, trainees, and cross-functional stakeholders
- Ability to work collaboratively with all employees at all levels
- Strong problem solving and critical thinking skills
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
80,000 - 120,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Strong practical and theoretical knowledge in their workintermediate
- Ability to gown into a cleanroom environmentintermediate
- Ability to be near strong magnetsintermediate
- Experience with delivering training to adult learners and groupsintermediate
- Effective communication between peers, trainees, and cross-functional stakeholdersintermediate
- Ability to work collaboratively with all employees at all levelsintermediate
- Strong problem solving and critical thinking skillsintermediate
Required Qualifications
- + years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience (experience)
- Bachelors in relevant science or engineering discipline, or equivalent in work experience (experience)
Preferred Qualifications
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing (experience)
- Experience and knowledge of Cell Therapy operations (experience)
Responsibilities
- Execute operations as described in standard operating procedures and batch records
- Complete documentation required by training policies and standard operating procedures
- Perform and demonstrate tasks in a manner consistent with safety policies, quality systems, and GMP requirements
- Qualify new employees on assigned curriculum required of their job functions
- Execute trainee requalifications as needed
- Ensure on-time completion of training assignments to ensure technical skills and knowledge are adequate prior to training others
- Collaborate with support groups on recommendations and solving training gaps between new hire onboarding and the transition to manufacturing operations
- Identify innovative solutions
- Support creation of manufacturing training materials such as On-The-Job-Trainings and Instructor-Led-Trainings
- Work independently and escalate issues appropriately, work with Management to resolve
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 Training Specialist, Cell Therapy Manufacturing in Devens, MA @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs