Associate Scientist, Analytical Development

Avid Bioservices•Tustin, CA

3d•$84,000 - $105,000•Onsite

About The Position

The Associate Scientist, Analytical Development will have the opportunity to focus on developing cell-based, ELISA, HPLC, and/or CE methods and will work alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. This position offers the chance to interface with Quality Control as methods are transferred into that group for cGMP testing, as well as to interface with external clients. The Associate Scientist will perform testing and sampling to support validation, process development, and stability studies in a non-GMP and GMP environment. They will have a substantial understanding of the job and apply knowledge and skills to complete a wide range of tasks, as well as support and lead continuous improvement initiatives.

Requirements

BS degree in Biochemistry, Chemistry, Biology or a related field is required.
5 + years of biotech industry experience working in a QC or analytical lab.
Previous experience with analytical testing and equipment utilizing analytical biochemistry methods, writing reports/procedures/specifications, GMPs and regulatory audits required.
HPLC, CE, or Potency/ELISA experience is essential.
Should have also have experience with protein characterization, electrophoresis, chromatography, and assay validation/qualification.
Previous experience in either HPLC, CE or Potency/ELISA assay methodologies is required.

Nice To Haves

A "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
Exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
Master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Responsibilities

Perform and review routine wet chemistry/ELISA/cell-based immunoassays, electrophoresis (SDS-PAGE/CE) and/or HPLC.
Use scientific reasoning when making decisions regarding the quality of the data reported. Research/gather information without supervision and make scientifically sound decisions based on knowledge and experience.
Train/supervise the experimental work of more junior analysts and may be a member of interdepartmental/tech transfer teams.
Develop, review, revise and write test methods, standard operating procedures and may perform trending analysis. May be designated as study lead for validation projects, investigations, and method development projects.
Knowledge of company cGMPs as well as industry regulations that apply to job functions. Participate in regulatory inspections.
Support continuous improvement initiatives.
Other tasks as assigned.