Operations Senior Analyst Supply Chain

Profile

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.

Operation Analyst/Senior Analyst - External Manufacturing & Strategic Sourcing - Cell Therapy Development Operations (CTDO)

Position Summary:

The Operation Analyst will be a member of External Manufacturing (EM) Project and Operations Management team. He/She will be a key resource in managing Change Controls and deviations for BMS Cell Therapy Contract Manufacturing sites around the globe. In addition to this responsibility, we are looking for an individual who can support external manufacturing other operational and project management functions. This role requires the ability to develop and maintain cooperative working relationships with team members to effectively close compliance related activities on time.

Job Responsibilities:

Initiate and manage Change Controls (CC) for EM and Strategic Sourcing Teams, ensure the CC are closely tracked till they are fully closed.

Initiate CMO notified deviations in BMS system. Follow up on CAPAs, work with team members, and QA to track and close them off.

Work closely with QA team to close internal CC & Deviation impacting CMOs.

Assist EM teams in other operational and project management functions as needed.

Assist in preparation of monthly dashboards and tracking KPIs for EM and Sourcing teams.

Create and maintain reports that are utilized by EM and Sourcing team to drive decisions and advance projects.

Leadership, Values and Behaviors:

Deliver business results through timely and quality decision making

Create an environment of teamwork, open communication, and sense of urgency

Drive strong collaboration across the company and amongst external partners

Build trust and effective relationships with peers, suppliers and stakeholders

Foster a culture of high ethics and compliance

Promote a mindset of continuous improvement, problem solving, and prevention

Education:

Bachelor's Degree, preferably in Engineering or Science

Requirements:

3-5 years of pharmaceutical GMP manufacturing clinical or commercial area

Experience in Quality or technical writing function is a plus

Experience working with compliance systems e.g. EQRM, Trackwise

Strong analytical, problem-solving, and critical thinking skills

Project management skills is a plus

Excellent organizational and time management skills

Excellent verbal and written communication skills

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

Req Number: R1526027_EN

Updated: 2020-06-12 00:00:00.000 UTC

Location: Summit,New Jersey

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.

Company info

Bristol-Myers Squibb Company
Website : http://www.bms.com