Associate Scientist, Clinical QC Bioanalytical- Cell Therapy
Working with UsChallenging.
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.
Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today.
With therapies only in their infancy and BMS's continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.
The QC Associate Scientist is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products.
This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot.
Additionally, when needed, this position will be able to assist with training and assay transfer.
Responsibilities:
Supports all activities related to the QC Bioanalytical team and laboratory operations including:
GMP release of drug product testing (drug product disposition) Documentation of GMP release activities Reagent and control qualification Method co-qualification and transfer Training new analysts Deviation, CAPA, Change Control management QC form and logbook management Perform peer review of testing data.
Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required Performs other tasks as required.
REQUIRED COMPETENCIES:
Basic knowledge/understanding of cGMP, FDA, USP, JP and EP regulations/guidelines as related to manufacture of cell therapy products.
Hands on experience with ELISA and Potency methods.
Advanced verbal, written communication skills.
Advanced ability to collaborate cross functionally to drive operational and quality excellence Advanced organizational and time management skills Demonstrated critical reasoning, problem solving, troubleshooting, investigation, and decision-making skills Advanced teamwork and collaboration Advanced mentoring and coaching, influencing, negotiating and personal interaction skills Requires strategic thinking and ability to work independently Demonstrated leadership and management skills, including establishing strategic direction and goals, and guiding execution while fostering a team-based environment Advanced knowledge of Quality Systems:
SOPs, Change Controls, Deviations, CAPAs, Complaints and Risk Assessments Ability to interpret/write general, technical, and complex technical documents Advanced knowledge and implementation of data integrity principles Ability to represent the department in audit and inspections Proficiency in standard Office software applications.
EDUCATION AND
Experience:
Bachelor's degree required, preferably in biology, Chemistry, Microbiology, or related science Advanced degree preferred An equivalent combination of education and experience may substitute.
Fluent in speaking/writing in English Minimum of 2-3 years of working experience in a cGMP regulated environment BMSCART#LI-OnsiteIf 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 CareersWith a single vision as inspiring as Transforming patients' lives through science(TM) , 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Recommended Skills Auditing Biology Clinical Works Coaching And Mentoring Communication Critical Thinking Estimated Salary: $20 to $28 per hour based on qualifications.
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.
Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today.
With therapies only in their infancy and BMS's continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.
The QC Associate Scientist is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products.
This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot.
Additionally, when needed, this position will be able to assist with training and assay transfer.
Responsibilities:
Supports all activities related to the QC Bioanalytical team and laboratory operations including:
GMP release of drug product testing (drug product disposition) Documentation of GMP release activities Reagent and control qualification Method co-qualification and transfer Training new analysts Deviation, CAPA, Change Control management QC form and logbook management Perform peer review of testing data.
Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required Performs other tasks as required.
REQUIRED COMPETENCIES:
Basic knowledge/understanding of cGMP, FDA, USP, JP and EP regulations/guidelines as related to manufacture of cell therapy products.
Hands on experience with ELISA and Potency methods.
Advanced verbal, written communication skills.
Advanced ability to collaborate cross functionally to drive operational and quality excellence Advanced organizational and time management skills Demonstrated critical reasoning, problem solving, troubleshooting, investigation, and decision-making skills Advanced teamwork and collaboration Advanced mentoring and coaching, influencing, negotiating and personal interaction skills Requires strategic thinking and ability to work independently Demonstrated leadership and management skills, including establishing strategic direction and goals, and guiding execution while fostering a team-based environment Advanced knowledge of Quality Systems:
SOPs, Change Controls, Deviations, CAPAs, Complaints and Risk Assessments Ability to interpret/write general, technical, and complex technical documents Advanced knowledge and implementation of data integrity principles Ability to represent the department in audit and inspections Proficiency in standard Office software applications.
EDUCATION AND
Experience:
Bachelor's degree required, preferably in biology, Chemistry, Microbiology, or related science Advanced degree preferred An equivalent combination of education and experience may substitute.
Fluent in speaking/writing in English Minimum of 2-3 years of working experience in a cGMP regulated environment BMSCART#LI-OnsiteIf 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 CareersWith a single vision as inspiring as Transforming patients' lives through science(TM) , 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 email protected .
Visit careers.
bms.
com/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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Recommended Skills Auditing Biology Clinical Works Coaching And Mentoring Communication Critical Thinking Estimated Salary: $20 to $28 per hour based on qualifications.
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