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Scientist, Quality Control Cell Therapy Bioanalytics

Posted on Jun 23, 2019 by Celgene

Warren, NJ 07059
Health Care
Immediate Start
Annual Salary
Req #:
Location: Warren, New Jersey, United States
Job Category: Quality
Work Location: 7 Powder Horn Drive 07059
Organization: Quality Control
Employee Status: Full-time
Job Type: Regular
QC Scientist, Cell Therapy Bioanalytics Summit, NJ
The QC Scientist is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Additionally, when needed, this position will be able to assist with training and assay transfer.

Required Competencies: Knowledge, Skills, and Abilities
  • Advanced hands-on experience with various analytical techniques including ELISA, qPCR, FACS and scientific knowledge in the characterization and transfer of pharmaceutical products.
  • Advanced ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements .
  • Advanced technical writing skill s .
  • Advanced problem - solving ability/mentality, technically adept and logical.
  • Ability to represent the interests of the gro u p on cross - functional team s .
  • Ability to set priorities of the group and manage timelines.
  • Ability to work with management locally and globall y .
  • Advanced a bi li t y to communicate effectively with peers, department management and cros s -functional peer s .
Duties and Responsibilities

Perform testing of in-process, final product, and stability samples.
  • Utilize scientific principles to assist in anal y tical testing methods and the proper use of laborato r y equipment.
  • Capable of handling complex issues and solving problems with only general guidance.
  • Prepare and present continuous improvement projects to management.
  • Comprehensive understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents.
  • Complete all work in a timely manner.
Perform peer review of testing data.
  • Review all data in accordance with applicable procedures and cGMP requirements.
  • Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
  • Complete all reviews in accordance with required release timelines.
  • Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required.
Train new analysts to general job duties.
  • Complete necessary training to become a qualified trainer.
  • Perform training effectively.
  • Document training per procedural and cGMP requirements.
Support document revision, project, CAPA, and investigation/deviation tasks.
  • Perform assigned tasks within a CAPA, deviation, or project
  • Participate in complex projects and continuous improvement efforts.
  • Take a leadership role, as required, for projects.
  • Draft and review technical documents, such as SOPs and protocols/reports.
  • Communicate effectively with management regarding task completion, roadblocks, and needs.
  • Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles.
  • Performs other tasks as a s signed.
Education and Experience
  • Bachelor s degree required, preferably in Science.
  • Advanced Degree preferred.
  • 5-8 y e ars o f relevant work experience, preferably in a regulated environment.
  • An equivalent combination of education and experience may substitut e.
Working Conditions
  • The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required.
  • The incumbent must analyze numerical values on a daily basis.
  • The incumbent will be working a laboratory setting, up to six ( 6) hours per day.
  • The incumbent will be working around bio hazardous materials, including chemical agents up to six ( 6) hours per day.
This job description is intended to describe the general nature and level of work being performed b y th e perso n assigne d t o thi s position . Th e primar y 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 seconda r y 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.

About Us


At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Our vision as a company is to build a major global biopharmaceutical corporation while focusing on the discovery, the development, and the commercialization of products for the treatment of cancer and other severe, immune, inflammatory conditions.

\"At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients.\"

There are more than 300 clinical trials at major medical centers using compounds from Celgene. Investigational compounds are being studied for patients with incurable hematological and solid tumor cancers, including multiple myeloma, myelodysplastic syndromes, chronic lymphocytic leukemia (CLL), non-Hodgkin s lymphoma (NHL), triple-negative breast cancer and pancreatic cancer. As committed as we are to clinical accomplishment, we are equally committed to patient support, which is a guiding principle at Celgene. We believe all who can benefit from our discoveries should have the opportunity to do so. Celgene puts patients first with industry-leading programs that provide information, support and access to our innovative therapies.
Associated topics: laboratory, medical technologist, microbiology, mls, pathology, scientist, sterile processing technician, technician i, technician iii, toxicology

Reference: 724559407