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QC Scientist, Sample Management CAR-T

Req #: 1801336
Location: Summit, NJ US
Job Category: Quality
Work Location: 556 Morris Avenue CELSUMWEST 07901
Organization: Celgene Corporation
Schedule: 40
Shift:
Employee Status: Full time
Job Type: Regular
Job Level:
Travel:
Other Locations:US- NJ- Summit West

Description

Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, ​quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.

Scientist - Sample Management, QC Systems and Services CAR-T

Summit, New Jersey

1.      Purpose and Scope of Position

The QC Scientist for Sample Management is responsible for the management of QC samples and materials in support of the analytical and microbiology CAR-T QC laboratories. This includes, but is not limited to, materials inventory management, retains management and sample tracking and delivery.

2.      Required Competencies: Knowledge, Skills, and Abilities

  • Proficient in the use of LIMS and sample tracking software
  • Working knowledge of Lean Labs
  • Proficient with enterprise applications
  • Experience with cold chain sample storage and transfers
  • Advanced ability to work in a collaborative team environment
  • Advanced ability to accurately and completely understand, follow, interpret and apply Global

Regulatory and cGMP requirements

  • Ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines
  • Ability to set priorities of the sample management group and manage timelines

3.      Duties and Responsibilities

      Manage Test Samples and Retains

  • Responsible for the management of test samples including receipt, storage, distribution and transfer and disposal
  • Responsible for the management and long-term storage of retains and reference samples
  • Maintain sample tracking and chain of custody records in accordance with cGMP requirements and written procedures
  • Ensure that obsolete/expired samples/materials are destroyed/disposed according to written procedures
  • Perform sample queries and periodic storage reports as required
  • Assist management with investigations and deviations related to sample management
  • Collaborate with other departments to identify and implement process efficiencies
  • Train laboratory and production personnel on the sample management process

Manage Lab Inventory

  • Responsible for inventory management of lab supplies including reagents, media, consumables, etc.
  • Responsible for reference standard inventory and distribution 
  • Ensure that materials are appropriately labelled and traceable as per appropriate cGMP, regulatory requirements, and written procedures
  • Assist management with investigations and deviations related to lab inventory
  • Implement 5S principles as appropriate
  • Implement FIFO as appropriate

           

QC Materials Support

  • Maintain sample management metrics
  • Facilitate Cold chain transfers as required
  • Liaise with supply chain, warehouse and lab service to ensure supply stocks
  • Performs other tasks as assigned

4.      Education and Experience

  • Bachelor’s Degree required, preferable in Science
  • Advanced Degree preferred
  • 5 - 8 years of relevant work experience, preferable in a regulated environment
  • An equivalent combination of education and experience may substitute

5.      Working Conditions

  • The incumbent should be able to distinguish colors and possess correctable vision to 20/20
  • The incumbent will be doing light to moderate lifting and carrying (or otherwise moves) objects under 15-20lbs
  • The incumbent will be working a laboratory setting up to six (6) hours per day.
  • The incumbent will be working around biohazardous materials, including chemical agents, up to six (6) hours per day.
  • The incumbent may be exposed to fluctuating and/or extreme temperature on occasions

This job description is intended to describe the general nature and level of work being performed by the person assigned to this positionThe 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 positionThere are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this jobEmployees holding this position will be required to perform any other job-related duties as requested by management.

#LI-POST

Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.
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About Celgene

Celgene is a global biopharmaceutical company committed to improving the lives of patients worldwide. At Celgene, we seek to deliver truly innovative and life-changing treatments for our patients.

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