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Quality Control Analyst, CAR-T Critical Reagents (1 of 4) - 2406183420W
Description
Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Control Analyst, CAR-T Critical Reagents (1 of 4)! This position will be located in Raritan, NJ.
_At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/._
Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR T platform and investigational treatment.
Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR-T team!
The Quality Control (QC) Analyst is responsible for preparing and conducting testing of critical reagents used by the QC laboratories. They are responsible for ensuring testing is completed in adherence with all applicable procedures, standards, and GMP regulations.
Key Responsibilities:
Conduct analytical testing to qualify critical reagents used in the CAR-T QC laboratories
Perform analytical testing in compliance with all applicable procedures, GMP, and GDP regulations
Ensure a safe work environment by following guidelines in environmental, health, and safety regulations
Perform peer review of laboratory data
Collaborate and coordinate with testing laboratories to acquire the data necessary to prepare documentation and issue Certificate of Analysis
Author and updateSOPs, WIs, and Protocols using the Document Management System
Support laboratory related investigation records and CAPAs
Assist in the execution of internal audits
Provide input to functional laboratory meetings
Provide input and take actions as a QC representative at cross-functional meetings
Qualifications
Education:
Experience and Skills:
Required:
Minimum two (2) years of relevant work experience
Knowledge of cGMP regulations and Good Documentation Practices (GDP)
Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, Flow Cytometry, ELISA, Cell Culture, and/or Potency assays
Excellent written and verbal communication skills
Preferred:
Experience in reagent qualification
Experience in a Quality Control setting
Experience within Biopharmaceutical or Pharmaceutical industry
Basic knowledge of compendial (e.g., USP, EP, JP, etc.) requirements pertaining to their functional area of QC
Work experience in Cell and/or Gene Therapy
Other:
There are 4 openings for this role with 3 of them being Monday-Friday Day shift, the 4th opening Requires ability and flexibility to work 8-hour shifts between the operational hours of 2:00pm - 10:00pm (Monday - Friday), and provide occasional support on the weekends or other shifts.
Requires up to 10% domestic travel to regional sites
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Employees are eligible for the following time off benefits:
Vacation – up to 120 hours per calendar year
Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
Holiday pay, including Floating Holidays – up to 13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
The anticipated base pay range for this position is 70,000- 126,000 USD$.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com .
Primary Location NA-US-New Jersey-Raritan
Organization Janssen Pharmaceuticals, Inc. (6062)
Travel Yes, 10 % of the Time
Job Function Quality Control
Req ID: 2406183420W