Sr. QC Associate
  • B.S. or advanced degree in Biology or a related science required with a minimum of eight (8) years experience on analytical bench working with analytical method qualification/validation and method transfer experience

TriLink Biotechnologies is a rapidly growing biotech firm in San Diego, CA that offers competitive wages and a full benefit package including medical, dental, vision, LTD, and a retirement plan.

TriLink is an EEO Employer.

  • Partner with internal and external customers to transfer, qualify, and/or validate new assays and methods

  • Independently conducts analyses and interprets results

  • Set up, troubleshoot, and make adjustments to laboratory equipment

  • Performs routine to complex laboratory analyses and experiments with no supervision

  • Transfer, modify, and improve analytical methods for Slot Blot, Fragment Analyzer, BioAnalyzer, Capillary Electrophoresis, qPCR and etc.

  • Serves as a technical lead on projects and provides direction to various levels of QC Associates

  • Compose Standard Operating Procedures (SOPs), Analytical Protocols, Analytical Reports and GMP documents

  • Method and system qualifications

TriLink Biotechnologies is seeking a Senior QC Associate. As part of the QC team at TriLink Biotechnologies, this individual will be responsible for Functional Assays Method Validation/Qualification and Method Transfer from internal development as well as from external customers. The role also requires to sustain the activities for QC Functional to support Assays for the core Manufacturing, Quality, R&D and GMP. This successful candidate will thrive in a fast-paced environment and will serve as a technical expert and in lab support for QC Functional for all equipment and method related needs.

  • B.S. or advanced degree in Biology or a related science required with a minimum of eight (8) years experience on analytical bench working with analytical method qualification/validation and method transfer experience
  • Demonstrated fundamental knowledge of various instruments and wet chemical analytical techniques
  • Solid understanding of theory and operating principles techniques of Slot Blot, Fragment Analyzer, BioAnalyzer, Capillary Electrophoresis, qPCR and etc.
  • Strong GMP and GLP background is highly desirable
  • Experience with ISO 9001 / 13485 preferred