Übersicht

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.

Just as Cell Therapy is redefining personalized medicine, we are creating the industry defining Cell Therapy Operations, for our patients, caregivers, providers and partners. Our global Cell Therapy Development and Operations team’s mission is to define and deliver the world’s most trusted cell therapy manufacturing and distribution network and to install and maintain the highest quality standards. This position will support in providing Quality oversight of Contract Manufacturing Organizations (CMOs) performing key manufacturing steps for CAR T products in Europe. The role will partner with the responsible Quality Manager and other internal stakeholders to maintain and improve the performance of our CMOs with focus on highest quality standards and GMP compliance. This professional will take responsibility for review of batch records for clinical and commercial CAR T intermediate products and internal release for further processing. Furthermore the candidate will partner with the Quality manager, the patient Operations group and our external European distribution hub to ensure timely delivery of the cell therapy products to the treatment sites.
She/He will be a part in the process of building a team and governance model for our external European partners in order to ensure successful commercialization and highest quality of our CAR T products for the benefit of our patients.

Key responsibilities

Support Senior Quality manager in providing Quality oversight of routine operations at CMOs in support of cell therapy (CAR T) intermediate product manufacturing
Responsible for batch record review of intermediate product (Make 1) and preparation of system release
Closing and remediation of detected gaps in collaboration with CMO
Partner with CMO Quality to ensure a robust batch release process in accordance with agreed processes and defined timelines
Oversee batch disposition status for European patients and ensuring availability and completeness of documentation required for final drug product release (QP release)
Support in review and approval of CMO deviation investigations, CAPA, controlled documents (Master records)
Support in review and approval of internal investigations and CAPA affecting the CMO
Partner with stakeholders across different operational functions and participate in projects in order to improve processes
Support and act in quality related improvement projects in collaboration with affected CMO functions
Support Senior Quality manager in providing quality oversight of routine operations for EU distribution center responsible for import, disposition and distribution of finished cell therapy product (CAR-T) in EU
Support in review and approval of deviation investigations, CAPA, change control, controlled documents linked to the European distribution center
Partner with patient operations group for resolution of real time issues during last mile delivery to treatment sites
Required Qualifications

Strong organizational skills, including ability to follow assignments through to completion.
Bachelor’s degree in biochemistry, biology, microbiology, chemistry, engineering, pharmacy or closely related areas or comparable education with experience in GMP industry.
First experience in EU GMP regulated industry within in quality assurance, quality control, or manufacturing
Knowledge of relevant regulations and guidance.
Able to work independently and reliable with regards to quality and timeframes
Very good verbal and written communication skills.
Ability to work in cross functional teams
Fluent in English and German

Preferred Qualifications

Experience within the Cellular Therapeutics environment.
Experience with biological manufacturing and related documentation
Ability to prioritize and successfully manage complex and competing tasks
Detail-oriented with expertise in problem solving and solid decision-making abilities.
Ability to work in a fast-paced environment