Bristol-Myers Squibb Company

Quality and Business Projects Lead

Location
Princeton, NJ, US
Posted
Oct 18, 2018
Ref
R1510713
Required Education
Bachelors Degree
Position Type
Full time
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.

One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support. 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.

Quality and Business Projects Lead reports into the head of GSRP and works closely with GSRP functional-area Leads to support quality, compliance and business objectives for the department.

The Quality and Business Projects Lead will:

• Establish a quality program that focuses on activities critical to achieving business goals and maintaining global compliance.

• Maintain a tracking process for critical quality attributes of GSRP work and periodically analyze the attributes against agreed Departmental standards.

• Assure that any CAPA responsibilities in the department are addressed in accordance with timelines, and assure follow through on CAPA requirements.

• Advise the business on operating process such as SOPs and related documents and will drive the maintenance of process and training activities with the functional area Leads and subject matter experts.

• Assist the head of GSRP with designing and delivering business projects that meet the strategic objectives of the Department

Position Requirements include (but are not limited to)
  • Experience in working with quality assessment and compliance in Pharma industry or closely related environment
  • Demonstrated abilities in risk identification, analysis, prevention and remediation
  • Takes initiative, demonstrates commitment and follow-through
  • Familiarity with regulatory operations processes and requirements
  • Ability to lead cross functional teams to deliver work activities
  • Ability to interact and negotiate with outside vendors when needed to deliver business projects
  • Strong organizational, communication, and influencing skills.
  • Needs to be able to effectively adjust plans to deal with constant change and the challenges that come with it.
  • Associate Director : A B.A. or B.S. in a relevant scientific, quality or business field with 6 years of pharmaceutical industry experience, or experience in a closely related field (such as medical device industry, health care quality, etc.)
  • Master's degree or additional training/certification in quality systems is desirable.