Supervisor QC Microbiology

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.

This is a Wed - Sat PM Shift (1:30p - midnight)

GENERAL SUMMARY

The QC Microbiology Supervisor is a full-time position. This role is responsible for the day to day operations associated with the in-process and release testing of clinical and commercial autologous cell therapy product. The QC Supervisor will be a key leader responsible for GMP operations and meeting critical business goals.

MINIMUM REQUIREMENTS

Education:

BS in a scientific discipline.

Experience

8 year of regulated industry experience

Knowledge, Skills, and Abilities

Strong working knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.

Demonstrated experience building and leading exceptional teams

Ability to apply Lean, Six Sigma and Risk Management concepts and tools is preferred.

Ability to work in a high paced team environment, meet deadlines, and prioritize work from multiple projects.

Strong analytical and communication skills as well as sound judgment, with the ability to work effectively with others.

Demonstrated success working in a high-performing, business results-driven environment.

ESSENTIAL DUTIES

Key Responsibilities

Provide supervision of Quality Control (QC) associates and oversees the day to day activities related to in-process, final release and stability testing of drug product.

Develops and manages a daily work plan for QC associates.

Hire, mentor and develop exceptional QC personnel.

Identifies and mitigates risks in QC labs that could negatively impact the safety, identity, strength purity or quality of the product.

Assists in the design, implementation and continuous improvement of Quality Control systems that are technically sound, promote effective and efficient operations, and comply with cGMP requirements.

Provides leadership support during trouble shooting of assay performance and equipment as it relates to ensuring the quality and compliance of the product.

Ensures deviations, CAPA, change controls, process transfers, and other business drivers are supported in a compliant manner.

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.

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, disability or protected veteran status.

Company info

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