Job Description

Working with Us
Challenging. Meaningful. Life-changing. Those aren\xe2\x80\x99t 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\xe2\x80\x99ll 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: .

PURPOSE AND SCOPE OF POSITION:

The QC Specialist is responsible for supporting Quality Control microbiology testing for the release of viral vector samples. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Additionally, the QC Specialist may assist with assay transfer activities. The Specialist, QC Microbiology role is stationed at the Vector Manufacturing Facility and reports to the Manager, QC Microbiology.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities

Knowledge of aseptic technique within a laboratory environment is preferred.

Hands on experience with various microbiology techniques including PCR, endotoxin and sterility testing is preferred.

Ability to accurately and completely understand, follow, interpret, and apply Global Regulatory and cGMP requirements.

Technical writing skills.

Problem-solving ability/mentality, technically adept and logical.

Ability to communicate effectively with peers, department management and cross-functional peers.

Knowledge of LIMS and laboratory data analysis systems preferred.

DUTIES AND RESPONSIBILITIES

Perform compendial verification, method transfer/validation, and routine testing of in-process, final product, and stability samples of cell therapy drug product in accordance with applicable procedures and cGMP requirements.

Perform environmental and clean utilities monitoring within the manufacturing environment.

Use scientific principles to assist with microbiological testing methods and the proper use of laboratory equipment.

Document data GMP accurately and within the proper system.

Anticipate and troubleshoot problems.

Train new analysts in general job duties.

Support document revisions, projects, and investigation/deviation related tasks.

Perform assigned tasks within a CAPA, deviation, or project.

Participate in projects and continuous improvement efforts.

Other duties as assigned.

Support for QC and manufacturing operations requires shift coverage consisting of weekdays, weekends, holidays, and during adverse weather conditions.

EDUCATION AND EXPERIENCE (As Applicable):

Bachelor\xe2\x80\x99s degree required, preferably in science.

2+ years of relevant work experience, preferably in a regulated environment.

An equivalent combination of education and experience may substitute.

Experience working in a GMP laboratory and with biologics/large molecule products preferred.

WORKING CONDITIONS: (US Only):

The incumbent will be required to gown to access classified manufacturing areas. Lighting and temperature are adequate and there are no abnormal conditions caused by noise, dust, etc.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

If you come across a role that intrigues you but doesn\xe2\x80\x99t 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 \xe2\x80\x9cTransforming patients\xe2\x80\x99 lives through science\xe2\x84\xa2 \xe2\x80\x9d, 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
Physical 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 . Visit 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.

Bristol-Myers Squibb