Associate II, Shop Floor Quality Assurance Cell Therapy - Bristol Myers Squibb
Devens, MA
About the Job
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
Position: Associate II, Shop Floor Quality Assurance Cell Therapy
Location : Devens, MA facility
12 Hrs. Night Shift position 6:00PM to 6:00AM, Rotating Panama shift schedule.
Key Responsibilities
+ Provide Quality on-the-floor oversight to Manufacturing/ QC/ Warehouse/ Supply Chain operations. Identify departures from approved procedures & responding to minor issues or escalating to senior members.
+ Perform and document operational verification per approved procedures.
+ Observe manufacturing operations and identify departures from clean room behaviors and aseptic techniques.
+ Provide quality oversight to maintenance operations and support of pre-approved return to service plans
+ Perform area walkthroughs to identify quality issues and support remediation to ensure the floor and operations are in adherence with cGMP and approved procedures.
+ Review manufacturing or testing records to ensure compliance with approved procedures. Communicate and resolve discrepancies and escalate as required.
+ Maintain compliance with assigned learning plan.
+ Support internal and external inspections as required.
+ Contribute to the assessment of discrepancies and initiation of quality events.
+ Participate in cross-department and cross-functional meetings, communicate in professional manner, and share data/ knowledge within team. Build relationships within direct team and partner functions.
Qualifications & Experience
+ Bachelor's degree in STEM field preferred.
+ High school diploma/ associate degree with equivalent combination of education and work experience may be considered.
+ 0-2 years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
+ Ability to understand, follow, and apply approved procedures.
+ Possess basic computer skills with knowledge of MS Office.
+ Ability to understand problems and propose practical solutions.
+ Ability to communicate effectively with cross functional peers and direct management through written and verbal skills.
+ Ability to work in a fast-paced team environment with changing priorities.
+ Detail oriented and task focused, with ability to meet deadlines and prioritize assigned work.
+ Ability to recognize the need for escalation of issues.
+ Self-motivated and willingness to learn.
#BMSCART #LI-Onsite #VETERAN
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1584813
Updated: 2024-11-29 07:36:05.555 UTC
Location: Devens-MA
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
Position: Associate II, Shop Floor Quality Assurance Cell Therapy
Location : Devens, MA facility
12 Hrs. Night Shift position 6:00PM to 6:00AM, Rotating Panama shift schedule.
Key Responsibilities
+ Provide Quality on-the-floor oversight to Manufacturing/ QC/ Warehouse/ Supply Chain operations. Identify departures from approved procedures & responding to minor issues or escalating to senior members.
+ Perform and document operational verification per approved procedures.
+ Observe manufacturing operations and identify departures from clean room behaviors and aseptic techniques.
+ Provide quality oversight to maintenance operations and support of pre-approved return to service plans
+ Perform area walkthroughs to identify quality issues and support remediation to ensure the floor and operations are in adherence with cGMP and approved procedures.
+ Review manufacturing or testing records to ensure compliance with approved procedures. Communicate and resolve discrepancies and escalate as required.
+ Maintain compliance with assigned learning plan.
+ Support internal and external inspections as required.
+ Contribute to the assessment of discrepancies and initiation of quality events.
+ Participate in cross-department and cross-functional meetings, communicate in professional manner, and share data/ knowledge within team. Build relationships within direct team and partner functions.
Qualifications & Experience
+ Bachelor's degree in STEM field preferred.
+ High school diploma/ associate degree with equivalent combination of education and work experience may be considered.
+ 0-2 years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
+ Ability to understand, follow, and apply approved procedures.
+ Possess basic computer skills with knowledge of MS Office.
+ Ability to understand problems and propose practical solutions.
+ Ability to communicate effectively with cross functional peers and direct management through written and verbal skills.
+ Ability to work in a fast-paced team environment with changing priorities.
+ Detail oriented and task focused, with ability to meet deadlines and prioritize assigned work.
+ Ability to recognize the need for escalation of issues.
+ Self-motivated and willingness to learn.
#BMSCART #LI-Onsite #VETERAN
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1584813
Updated: 2024-11-29 07:36:05.555 UTC
Location: Devens-MA
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Source : Bristol Myers Squibb