Quality Control Technician II

Invivoscribe Technologies Inc.
Job Location
San Diego, CA 92121
Salary is commensurate with experience.
  • Competitive salary that is commensurate with experience.
  • IVS provides health, dental, and vision coverage, Life/AD&D, short-term and long-term disability, paid vacation, sick time and holidays and a 401(k) retirement plan with generous employer match, among other benefits.
Job Description
  • Assists in addressing and documenting product inquiries

  • Effectively maintains the Standard Operating Procedures (SOP), acceptance criteria, etc., for the department and the products tested.

  • Assists in complaint analysis, troubleshooting and completing complaint documentation.

  • Effectively and efficiently test raw materials, in-process and final product and generate testing data.

  • Conducts and maintains the real-time stability study testing.

  • Maintains inventory materials used in quality control.

  • Conducts training.

  • Cooperates and respectfully communicates with external and internal customers.

  • Other duties, as assigned.

  • Working knowledge of polymerase chain reactions, gel electrophoresis, capillary electrophoresis, next generation sequencing, DNA/RNA isolation and purification, and cDNA synthesis.

  • Working knowledge of the following equipment is preferred: ABI capillary electrophoresis instruments (3130xl and 3500xl), ABI 7500 dx, PGM, MiSeq, BioTek plate fluorometer, and single and multichannel pipettes.

  • Working knowledge with medical device quality and regulatory requirements including QSR and ISO quality system standards and the IVD Directive is preferred.

  • Working knowledge of the use of Adobe Acrobat, Illustrator, and Photoshop.

  • Technical support experience.

  • Attention to detail.

  • Ability to follow Standardized Operating Procedures (SOPs).

  • Ability to work independently, as well as in a team environment.

  • Excellent communication skills with the ability to train employees.

  • Ability to manage multiple projects and changing priorities.

  • Willingness to learn and take on new challenges.

Education and Experience

  • Requires knowledge and skills normally acquired through the successful completion of a BS Degree in a scientific discipline.

  • 2-4 years of experience in a GMP-regulated industry or equivalent combination of education and experience.

About Our Organization

Invivoscribe Technologies, Inc., is a privately-held corporation dedicated to improving the quality of healthcare worldwide by providing high quality, reliable, cutting-edge tools for molecular research, molecular diagnostics, and personalized molecular medicine.

Invivoscribe provides a comprehensive selection of PCR-based gene rearrangement, chromosome translocation, and gene mutation Research Use Only testing reagents and controls. We also provide CE-marked in vitro diagnostic products to customers outside North America, and our subsidiary. Customers include many of the world's leading pharmaceutical and biotechnology companies, medical centers, cancer research centers, reference laboratories and molecular testing centers.

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