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Bristol Myers Squibb Senior Manager - Analytical Development in Summit, New Jersey

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 .

Title: Senior Manager - Analytical Development

Location: Summit, NJ

At Bristol Myers Squibb we are reimagining the future of cell therapy . With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team.

The Senior Manager, Analytical Development will be managing analytical technical team and develop and report KPIs for analytical Lab Operations performance and oversee commercial programs testing. Maintain high team performance and drive continuous improvement initiatives using operational excellence tools. Collaborate with managers across the analytical and QC network to harmonize best practices.

Key Responsibilities:

  • Oversee analytical team/s to ensure effective, timely and efficient operations and compliance with GLP/cGMP requirements.

  • Lead by example to foster a culture of teamwork and operational excellence and embed BMS values within operational activities.

  • Develop and report KPIs for Lab Operations performance. Maintain high team performance and drive continuous improvement initiatives using operational excellence tools.

  • Hire, mentor and develop team members to support business operations. Provide developmental feedback, coaching, and create a collaborative environment to enhance team performance and integration across site departments.

  • Approve investigations and creation of meaningful CAPA for improved lab performance.

  • Foster collaboration and communication across shifts and also between Technical Operations team members

  • Perform other tasks as required to support the analytical laboratories

  • Advanced ability to work collaboratively in a high-paced team environment, meet deadlines, and prioritize work from multiple teams.

  • Demonstrated leadership and management skills, including establishing strategic direction and goals, and guiding execution while fostering a team based environment.

  • Ability to work in a highly regulated environment and follow regulatory requirements and GLP/GMPs.

Qualifications & Experience:

  • Bachelor's degree or equivalent required, preferably in science. Advanced Degree preferred.

  • 10+ years of relevant laboratory work experience, preferably in a regulated environment. An equivalent combination of education and experience may substitute.

  • Experience with various bioanalytical techniques (cell-based assays, ELISA, qPCR, flow cytometry) and associated equipment preferred.

  • Minimum of 4 years of leadership experience required including management of direct reports.

  • Demonstrated success working in a high-performing and results driven environment.

  • Knowledge of LIMS, ELN and laboratory data analysis systems preferred.

  • Strong analytical, problem-solving, and critical thinking skills.

  • Sound experience of data handling and applied statistics.

  • Experience with Quality Management System (e.g. Deviations, CAPAs, Change Management)

  • Previous experience in manufacturing and quality testing of cell therapies, or product life cycle management is highly desirable

  • Previous experience in managing direct technical staff is preferred.

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BMSCART

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 scienceā„¢ , 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/ 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.

Company: Bristol-Myers Squibb

Req Number: R1583546

Updated: 2024-08-22 04:49:29.819 UTC

Location: Summit West-NJ

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.

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