Celgene

Specialist, Master Data

Posted on: 8 Mar 2021

Summit, NJ

Job Description

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.

PURPOSE AND SCOPE OF POSITION:

The Specialist, Master Data is responsible for the master data design and entry, on-site technical support, troubleshooting and problem resolution, end user training, and change management for the site manufacturing execution system (MES) and Enterprise Resource Planning (ERP) system. Specialists work with IT, manufacturing, engineering, quality assurance, and quality control to deliver master data changes in MES and the ERP. The position occasionally supports peers with recipe development in MES. The position requires strong project management skills and coordination with various other functional areas. The position works under the guidance of lead team members. recipe development, implementation, and support model. This position is key to the continued progression of our global MES strategy which includes a centralized recipe development, implementation, and support

The Process & Technology department supports manufacturing systems at the Summit S12 and Warren sites for cellular therapy manufacturing at Bristol Myers Squibb. This position is key to the continued progression of our global MES strategy which includes a centralized recipe development, implementation, and support model.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:

* Advanced time management skills, including ability to prioritize and manage expectations
* Advanced proficiency in Microsoft Excel & Visio
* Intermediate knowledge of manufacturing execution systems and ERP systems
* Intermediate knowledge of qualification and validation requirements in a regulated environment
* Intermediate knowledge of GMP manufacturing
* Intermediate technical writing skills
* Basic presentation development and delivery skills
* Basic knowledge of cGMP regulations
* Ability to provide accurate estimates and effectively communicate status of deliverables
* Ability to gown into Grade C and D classified environments
* Ability to provide on-call support in case of emergent issues
* Ability to travel < 10% of time
* Ability to work independently for extended periods of time
* Ability to work in a collaborative environment

Education and Experience:

* Bachelors degree in a related field from an accredited college or university required.
* Minimum of 5 years relevant work experience required, preferably in a pharmaceutical manufacturing environment.
* 1 year of experience supporting an MES and/or ERP system, preferably Syncade MES and Oracle ERP.
* An equivalent combination of education, experience and training may substitute.

WORKING CONDITIONS (US Only):

The incumbent will be required to gown to access classified manufacturing areas.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

BMSCART

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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Celgene

Summit, NJ

Celgene Corporation, a biopharmaceutical company, discovers, develops, and commercializes therapies for the treatment of cancer and inflammatory diseases worldwide. It offers REVLIMID, an oral immunomodulatory drug for multiple myeloma (MM), myelodysplastic syndromes (MDS), and mantle cell lymphoma; POMALYST/IMNOVID to treat multiple myeloma; OTEZLA, a small-molecule inhibitor of phosphodiesterase 4 for psoriatic arthritis and psoriasis; and ABRAXANE to treat breast, non-small cell lung, pancreatic, and gastric cancers.

The company’s products also include IDHIFA for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (rrAML) with an isocitrate dehydrogenase-2 mutation; VIDAZA, a pyrimidine nucleoside analog for intermediate-2 and high-risk MDS, chronic myelomonocytic leukemia, and AML; THALOMID to treat patients with MM; and ISTODAX, an epigenetic modifier. Its preclinical and clinical-stage product candidates include small molecules, biologics, and cell therapies for immune-inflammatory diseases, myeloid diseases, epigenetics, protein homeostasis, and immuno-oncology.

The company has agreements with BeiGene, Ltd; Acceleron Pharma, Inc.; Agios Pharmaceuticals, Inc.; bluebird bio, Inc.; Lycera Corp.; Juno Therapeutics, Inc.; EXSCIENTIA LTD.; and IMIDomics SL, as well as immuno-oncology collaboration with Sutro Biopharma. Celgene Corporation was founded in 1980 and is headquartered in Summit, New Jersey.