Scientist, CTTO Analytical Testing
Job
Bristol-Myers Squibb
Remote
$111,651 Salary, Full-Time
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Job Description
Scientist, CTTO Analytical Testing Summit, NJ Job Details Full-time $100,960
- $122,343 a year 1 day ago Benefits Paid holidays Disability insurance Health insurance Dental insurance 401(k) Paid time off Employee assistance program Vision insurance Life insurance Paid sick time Qualifications Quality control corrective actions Stability testing Immunoassays Technical documentation Immunological laboratory techniques Pharmaceutical regulatory compliance Bachelor of Science Data analysis skills Corrective and preventive actions (CAPA) GMP Technical report writing Molecular biology techniques Laboratory staff training Bachelor's degree Continuous improvement Doctor of Philosophy Team management Scientific protocols Master of Science Pharmaceutical analysis Laboratory compliance Laboratory staff supervision Technical skills instruction 1 year Senior level Cross-functional collaboration Project leadership Project stakeholder communication Cross-functional communication Stakeholder management Full Job Description Working with Us Challenging.
Read more:
careers.bms.com/working-with-us .PURPOSE AND SCOPE OF POSITION
The Cell Therapy Technical Operation (CTTO) Scientist is responsible for supporting the analytical testing at Analytical Testing group within CTTO during commercial phase. This group is responsible for flow-cytometry and molecular based sample testing for process robustness, stability, comparability, validation, training , technical transfer and other critical support as needed. This includes the ability to interface with multiple cross-functional stakeholders, the ability to independently perform tasks, interpret results, and troubleshoot.DUTIES AND RESPONSIBILITIES
Perform cell based in-vitro flow instrument, ELISA, qPCR assays. Perform testing on process characterization, comparability, stability and investigational samples. Perform peer review of testing data. Review all data in accordance with applicable procedures and cGMP requirements. Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. Complete all reviews in accordance with required release timelines of reagents. Utilize scientific principles to lead and support troubleshoot analytical testing methods and the proper use of laboratory equipment. Lead, manage, and support moderately complex projects, analytical technology transfer activities, and continuous improvement efforts. Comprehensive understanding of regulatory guidelines and can independently develop, write, and execute methods, protocols, reports and other related technical documents, such as SOPs. Lead, manage, and support document writing, revision, project, CAPA, and investigation/deviation tasks. Effectively train new analysts on analytical methods, instrument operation, and general job duties. Complete necessary training to become a qualified trainer. Manage and oversee junior scientist. Communicate effectively with peers, and demonstrate teamwork, with regards to review of results and corrections required. Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles. Communicate effectively with management regarding project updates, task completion, roadblocks, and needs. Capable of handling complex issues and solving problems with only general guidance. Complete all work in a timely manner.EDUCATION AND EXPERIENCE
Bachelor's degree required, preferably in science, advanced d egree preferred. BS degree with minimum of 5 years of relevant experience, or MS degree with minimum 2 years of relevant experience, or PhD degree with minimum of 1 years of relevant experience in analytical development, analytical testing, and/or analytical method technical transfer, preferably in a regulated environment. Demonstrated experience working with polychromatic flow-cytometry panels, flow-cytometry data analysis, ELISA and qPCR preferred. The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required. The incumbent must analyze numerical values on a daily basis. The incumbent will be working a laboratory setting up to six (6) hours per day. The incumbent will be working around biohazardous materials, including chemical agents up to six (6) hours per day.REQUIRED COMPETENCIES
(Knowledge, Skills, and Abilities): Advanced hands-on experience with various analytical techniques including flow-cytometry, molecular techniques and scientific knowledge in the characterization and transfer of pharmaceutical products. Advanced ability to accurately understand, follow, interpret, and apply global regulatory and cGMP requirements. Advanced technical writing skills, problem-solving ability/mentality, technically adept and logical thinking. Ability to represent the interests of the group on cross-functional teams. Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects. Ability to work with management locally and globally. Advanced ability to communicate effectively with peers, department management and cross-functional peers. 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.Compensation Overview:
Summit West- NJ•
US:
$100,960- $122,343 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis.
Our benefits include:
Health Coverage:
Medical, pharmacy, dental, and vision care.Wellbeing Support:
Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).Financial Well-being and Protection:
401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off US Exempt Employees:
flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees:
160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility- , additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Eligibility Disclosure:
T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. 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 a supportive culture, promoting global participation 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 an 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. Supporting People with Disabilities 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 careers.bms.com/ eeo- accessibility to access our complete Equal Employment Opportunity statement.
R1600726
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