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 jnj.com

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Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

Professional

All Job Posting Locations:

Raritan, New Jersey, United States of America

Job Description:

Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Analyst, Quality Control Analytics - CAR-T in Raritan, NJ! This shift is going to be scheduled 4:00pm - 2:00am through Sunday - Wednesday.

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/.

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 QC Analyst is responsible for conducting biochemical, microbiological, and/or general testing of final product samples submitted to the QC laboratories. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 – 15 other Analysts within the functional laboratory of the Quality Control department.

Key Responsibilities:

• Perform analytical testing and maintain a safe work environment in compliance with all applicable procedures, EHS, and GMP regulations

• Perform peer review/approval of laboratory data and logbooks

• Use electronic systems (e.g., LIMS, iLAB) for execution and documentation of testing

• Build, review, and approve relevant QC documents, SOPs, and WIs

• Complete invalid assay and general laboratory investigation records, CAPAs, change controls

• Support Health Authority inspections

• Provide input to functional laboratory meetings

Qualifications:

Education:

• Minimum of a Bachelor’s or equivalent University Degree required; advanced degree (MSc., Ph.D.) or focused degree in Biology, Biochemistry, Chemistry, or related scientific field is preferred

Experience and Skills:

Required:

• Minimum of two (2) years of relevant work experience

• Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, Flow Cytometry, ELISA, Cell Culture, and/or Potency assays

• Experience within Biopharmaceutical or Pharmaceutical industry

• Experience with aseptic processing in biosafety cabinets and/or ISO 5 clean room

• Demonstrated experience successfully working in an analyst role/level and proficiency using analytical methodologies within a functional laboratory

• Knowledge of cGMP regulations and Good Documentation Practices (GDP)

• Experience with Quality Control document reviews and regulatory inspection processes

• Proficient in performing technical writing (e.g., test methods, SOP's, protocols, etc.)

• Excellent written and verbal communication skills

Preferred:

• Work experience in Cell and/or Gene Therapy or Biologics

• Basic knowledge of Compendial (e.g., USP, EP, J