Upstream Process Development & Manufacturing Associate (2)

· San Diego, California
Employment Type Full-Time
Compensation DOE+Benefits+Options

ABOUT US

 

Sorrento is a clinical stage, antibody-centric, biopharmaceutical company developing new therapies to turn malignant cancers into manageable and possibly curable diseases. Sorrento's multimodal multipronged approach to fighting cancer is made possible by its' extensive immuno-oncology platforms, including key assets such as fully human antibodies ("G-MAB™ library"), clinical stage immuno-cellular therapies ("CAR-T"), intracellular targeting antibodies ("iTAbs"), antibody-drug conjugates ("ADC"), and clinical stage oncolytic virus ("Sephrevir®").

 

We attract smart people who play well with others. We're small enough for your ideas to make a big impact, and large enough to offer you opportunities to grow professionally at any stage of your career.

 

If you’re a quick learner, enjoy working in the biotech industry, and share our mission of providing ground-breaking impact to medicine, each other, and our patients, Sorrento Therapeutics is the place for you!


WHAT YOU’LL DO:


Our Upstream Antibody Process Development & Manufacturing team is currently seeking a Manufacturing Associate who will be responsible for performing Upstream Process Development/manufacturing tasks including cell culture, cell banking, benchtop bioreactor operation, media preparation, and assistance in single use bioreactors operation for production of clinical and commercial antibody products.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:


  • Maintain laboratory inventory and equipment.
  • Timely execute all aspects of upstream mammalian cell culture operations, including thawing and freezing cell lines, transfection, single cell sorting, cell expansion, fed-batch, assembly and operation of benchtop bioreactors, and harvest clarification.
  • Prepare media and buffer solutions as required.
  • Assist in the operation of Single-Use Bioreactors, including the Wave Cellbag and 100L, 500L, and 2000L bioreactors.
  • Records cell culture, process development activities and results in appropriate notebooks and spreadsheets.
  • Review and revise current Good Manufacturing Practice (cGMP), Batch Production Records, SOPs, protocols, and reports.
  • Provide support to cross-functional teams to meet production or timeline demands.
  • Demonstrate understanding in technical operations, safety, and cGMP.
  • Ensure the completeness and accuracy of manufacturing documentation per approved procedures.


EDUCATION AND QUALIFICATIONS:

  • Bachelor’s degree in life sciences majors is preferred. Other relative majors with knowledge background of cellular and molecular biology are also acceptable.
  • Mammalian cell culture experience is a plus.
  • Experience in current Good Manufacturing Practice (cGMP) environment is a plus.
  • Research experience is highly preferred.
  • Must be familiar with Word and Excel.

 

YOUR REWARD:

 

  • Support scientists who are on the leading edge of immunotherapies for the treatment of cancer. 
  • Earn a competitive salary that allows you to focus your attention on your passion.
  • A comprehensive benefits package including: medical, dental, vision, life and disability insurance, matching 401k, 10 paid holidays, and three-weeks’ PTO, plus stock options.

 

If this sounds like the right career to fit your interests, please apply. We’re looking forward to meeting you! 

 

Principals only. Recruiters, please don't contact this job poster. 

Sorrento Therapeutics, Inc. is an Equal Opportunity Employer

Thank You

Your application was submitted successfully.

  • Location
    San Diego, California
  • Employment Type
    Full-Time
  • Compensation
    DOE+Benefits+Options