Research Associate, Analytical Development

Avid Bioservices•Tustin, CA

1d•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 using cell-based assays, ELISA, HPLC, CE, PCR, SDS-PAGE, and related techniques. The position also interfaces with Quality Control when methods are transferred for cGMP testing. This is a full-time, onsite role. Work 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 required. Compensation is $31.15–$38.94 per hour, depending on experience and qualifications, with performance-based bonuses and benefits.

Requirements

Bachelor's degree in Biological or Physical Sciences.
At least 2 years of relevant experience and 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.
Strong written and verbal communication skills.
Multitasking ability and attention to detail.
Ability to work collaboratively and build relationships with team members and external contacts.

Nice To Haves

Experience in assay validation or qualification.
Familiarity with 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, and 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 laboratory 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.