J

Johnson & Johnson

Makes prescription drugs and medical devices

Analyst, Quality Control Analytics - CAR-T - Analytics

Regulatory & Quality (Life Sciences)Posted on Nov 10
Full-timeRaritan, NJ, USA$66k - $107k

About the Job

Requirements

  • A bachelor's or equivalent university degree is required.
  • At least two years of relevant work experience is required.
  • Experience performing one or more cellular or molecular techniques, including qPCR, flow cytometry, ELISA, cell culture, or potency assays, is required.
  • Experience in the biopharmaceutical or pharmaceutical industry is required.
  • Experience with aseptic processing in biosafety cabinets and/or an ISO 5 clean room is required.
  • Demonstrated experience working at an analyst level and proficiency using analytical methodologies within a functional laboratory are required.
  • Knowledge of current Good Manufacturing Practice (cGMP) regulations and Good Documentation Practices (GDP) is required.
  • Experience with Quality Control document reviews and regulatory inspection processes is required.
  • Proficiency in technical writing, such as test methods, standard operating procedures, and protocols, is required.
  • Excellent written and verbal communication skills are required.
  • Ability and flexibility to work 10-hour shifts between 8:00 a.m. and 6:00 p.m. Sunday through Wednesday, with occasional weekend or other-shift support, is required.
  • Ability to lift up to 20 pounds, stand or sit for extended periods in a laboratory setting, perform visual inspections of materials, and document observations during laboratory testing is required.
  • Ability to travel domestically up to 5% is required.

Responsibilities

  • Conduct biochemical, microbiological, and/or general testing of final product samples submitted to QC laboratories while complying with applicable procedures, standards, and GMP regulations.
  • Perform analytical testing and maintain a safe work environment in compliance with applicable procedures, EHS, and GMP regulations.
  • Perform peer review and approval of laboratory data and logbooks.
  • Use electronic systems such as LIMS and iLAB to execute and document testing.
  • Build, review, and approve relevant QC documents, standard operating procedures, and work instructions.
  • Complete invalid assay and general laboratory investigation records, CAPAs, and change controls.
  • Support Health Authority inspections.
  • Provide input to functional laboratory meetings.

Desired Qualifications

  • An advanced degree (MSc or Ph.D.) or a focused degree in Biology, Biochemistry, Chemistry, or a related scientific field is preferred.
  • Work experience in cell and/or gene therapy or biologics is preferred.
  • Basic knowledge of compendial requirements and standards, such as USP, EP, or JP, is preferred.
  • Experience with LIMS and SAP or equivalent systems is preferred.
  • Experience, training, or certification with Process Excellence tools and methodologies is preferred.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

Recently Posted Jobs

Explore more opportunities at Johnson & Johnson

See more jobs