Research Associate, Analytical Development

Avid Bioservices•Tustin, CA

110d•$31 - $39•Onsite

About The Position

Avid Bioservices is seeking a Research Associate to join its Analytical Development team, which develops analytical methodologies for protein biologics. The role works closely with analytical Scientists to identify and characterize protein biologics, developing methods such as cell-based assays, ELISA, HPLC, CE, PCR, and/or SDS-PAGE. The Research Associate also interfaces with Quality Control when methods are transferred for cGMP testing. This is a full-time, onsite position. Schedules are Monday through Friday, 8:00 a.m. to 5:00 p.m.; Sunday through Wednesday, 7:00 a.m. to 6:00 p.m.; or Wednesday through Saturday, 7:00 a.m. to 6:00 p.m., unless otherwise stated by the Supervisor. Overtime may be necessary. The hourly compensation range is $31.15 to $38.94, depending on experience and qualifications. The company also describes opportunities for career growth and development and a supportive, inclusive work environment.

Requirements

Bachelor's degree in Biological or Physical Sciences.
At least 2 years of relevant experience.
Demonstrated working knowledge of scientific principles.
Experience with analytical method development using bioanalytical techniques.
Experience with at least one of the following: ELISA, cell-based assays, HPLC, CE, icIEF, PCR, or SDS-PAGE.
Ability to work overtime as necessary.
Strong written and verbal communication skills.
Exceptional multitasking skills and attention to detail.
Ability to build relationships with team members, clients, vendors, and suppliers.
Positive, team-oriented approach.

Nice To Haves

Experience in assay validation or qualification.
Knowledge of industry regulations applicable to the job functions.

Responsibilities

Perform laboratory tasks supporting the development, optimization, validation, and routine testing of protein therapeutics using protein characterization techniques.
Use one or more of the following techniques: ELISA, cell-based assays, HPLC, CE, icIEF, PCR, or SDS-PAGE.
Document method development and validation activities according to current practices.
Assist in training analysts on new methods and transfer methods to the cGMP Quality Control lab, as necessary.
Work in a fast-paced team environment, meet deadlines, and prioritize work.
Provide regular updates to the Process Development department and other functional teams as necessary.
Perform other tasks as assigned.