Molecule Quality Lead

Profile

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Summary:

Key responsibilities of the Associate Director, Molecule Quality include: 1) Design and implement end-to-end quality strategy for assigned Molecule; 2) Ensure successful Health Authority (HA) engagement; 3) Manage for cause, critical and/or complex quality issues as well as serious breaches for the assigned molecule; 4) Engage in appropriate activities to support product submissions; 5)Establish strong partnership with business stakeholder.

Responsibilities:


Design and implement the quality strategy for the molecule
Assess specific risk areas - brings ideas and strategies to the forefront and propose modifications to the Quality Assurance Program where necessary
Identify and drive continuous quality process improvements as a consequences of audits, assessments, inspections, trends/metrics and root cause analysis
Lead implementation of Quality by Design principles for the molecule
Develop, implements and maintain the molecule quality plan summarizing the quality strategy by summarizing the result of evidence of quality activities
Integrate end -to end quality principles and review project milestones with R&ED/GDD
Establish strong partnership with business stakeholder
Seek to understand and evaluate their priorities
Actively participate in and make meaningful contributions
Deliver independent expert support and propose solutions
Present key data (compliance, conformance, issues and risks) to drive decision making
Manage for cause, critical and/or complex quality issues as well as serious breaches for the assigned molecule
Engage in appropriate activities to support product submissions
Ensure successful Health Authority engagement
Demonstrate implementation of quality strategy to Health Authorities
Create quality plan to be shared with Health Authorities
Prepare for inspections and support inspections
Provide guidance and training on relevant GxP regulations and guidelines to cross-functional business partners.


Degree/Certification/Licensure


B.S. and/or M.S. in Chemistry, Biology, or Health or Quality related field or equivalent combination of education, training and experience


Experience - Responsibility and minimum number of years


Mnimum 8 years QA experience or relevant experience in medical quality management, biomedical science, clinical development, or regulatory compliance


Competencies - knowledge, skills, abilities, other


Demonstrated strong knowledge of ICH/GCP, regulatory guidelines/directives, clinical research processes and principles of Quality Assurance
Understanding of BMS's therapeutic areas (Oncology, Cardiovascular, Hematology, Cell Therapy and Immunology and Fibrosis)
Demonstrated applied knowledge of clinical/pharmacovigilance and regulatory requirements, as well as analytical, organizational and planning skills
Broad knowledge of applied risk-management including risk assessment, risk analysis, risk evaluation, risk reporting and communication, risk treatment and the review of continuous risk management
Experience in regulatory inspection preparation, management, and related follow-up
Proven problem-solving skills to prevent and overcome complex process and quality related issues during clinical program implementation and execution
Proficiency in utilizing data to generate insight and to formulate clear business questions that can be answered with data
Communication Skills: Communicates professionally, clearly, concisely and consistently both verbally and in writing to internal and external customers; excellent presentation skills for compelling peer and Senior Management communication
Project Management: Must be able to manage projects and deliver all expected deliverables in a timely manner and proactively communicate changes in pre-established goals and deadlines
Responds resourcefully to changing business conditions and opportunities, proactively looking for ways the organization can adapt its plans, tactics, or strategies


Software that must be used independently and without assistance (e.g., Microsoft Suite )


Microsoft Suite, Veeva Vault QMS, SharePoint, other systems as assigned/applicable


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Company: Bristol-Myers Squibb

Req Number: R1527930_EN

Updated: 2020-07-24 00:00:00.000 UTC

Location: Princeton,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.

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