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Senior Scientist, Manager REF STDS

Employer
Bristol Myers Squibb Company
Location
New Brunswick, NJ, United States
Start date
Aug 9, 2019

View more

Discipline
Science/R&D, Biotechnology
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Pharm Country, Best Places to Work

Job Details

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

This mission critical position is responsible for the support of pharmaceutical operational activities for the Reference Standard and Critical Reagent (RSCR) Group within the Global Quality Analytical Science & Technology (GQAST) organization. Primary role will be to support project / product interactions and operational needs within the RSCR Operations group including ownership and facilitation of key aspects for the small molecule side of the business.

Responsibilities:

Manage small molecule pharmaceutical standards portfolio resources and scheduling to attain project deliverables and coordinate project communication for all stakeholders. Ensure problem solving and decision making addressing major risks and issues by identifying, documenting, resolving, communicating or escalating to senior leadership when appropriate. Collaborate with key stakeholders to manage expectations. Develops and drives detailed plans, identifying critical path and timing while meeting strategic intent and achieving key milestones. Influence key stakeholders, develop communications strategy, approach and plan. Lead project-related activities including meetings, recurring status meetings, reporting, risk tracking, and conflict resolution as needed. Closely monitor key aspects of the business such as inventory and burn rate analysis, and actively participate in investigations and providing filing support. Foster diverse/inclusive high performance teams and maintain strong relationships with operational and functional leadership.

QUALIFICATIONS

Specific Knowledge, Skills, Abilities, etc:

  • Must have industry experience working with or managing the testing of pharmaceutical reference standards and/or working within or managing complex pharmaceutical operational programs (reference standards, stability, etc.)
  • Must be capable of working in a highly energized and matrixed work environment.
  • Must have prior leadership experience within a technical field, preferably within the biotech or pharmaceutical industry.
  • Must demonstrate teamwork, project planning, strong organizational skills, computer competency, and effective written and verbal communications within both structural and matrix organizations.
  • To be successful in this role, the candidate must embrace collaboration with partners, customers, and team members, while operating with integrity, as well as seeking and participating in the continuous improvement of systems and culture.
  • Prior experience in the pharma industry, specifically in the area of sample and data management for pharmaceutical programs is desirable.


Education/Experience/ Licenses/Certifications:

A BS, MS, or PhD in biological sciences, chemistry or related scientific disciplines with at least 5 to 8 years of experience in the biotech or pharmaceutical industry. Preferably, the ideal candidate will also have experience either managing or supporting clinical or commercial pharmaceutical programs.

Physical Demands / Work Environment:

- This is a leadership role for commercial and clinical programs, including lab work, office work, teleconferencing, computer work, and running meetings. Including ...
  • Sitting / standing
  • Walking-Level Surfaces
  • Repetitive (Use of arms, hands, wrists)
  • Inside Work
  • Working in a Team
  • Working with/around others


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 the resources to pursue their goals, both at work and in their personal lives.

Company

Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

At Bristol Myers Squibb, we believe in the power of science to address some of the most challenging diseases of our time. Our focus on these unmet needs comes during a remarkable time, when unprecedented scientific breakthroughs are advancing the treatment of disease as never before in human history.

We work every day to transform patients’ lives through science. Each day, our employees around the world work together for patients – they are at the center of everything we do. They inspire us. They are the reason we come to work each day.

We combine the agility of a biotech with the reach and resources of an established pharmaceutical company to create a global leading biopharma company powered by talented individuals who drive scientific innovation.

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Company info
Website
Phone
+1-800-332-2056
Location
430 E. 29th St
14th Floor
New York
New York
10016
United States

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