Research Associate, Analytical Development

BioTalent; Tustin (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

BioTalent in California is seeking a Research Associate to join Analytical Development, focusing on developing and validating protein biologics methods. You will work with experienced scientists to identify and characterize protein biologics and develop methods such as ELISA, Cell-based assays, HPLC, CE, iCIEF, PCR, and SDS-PAGE, with transfer to cGMP QC.

The role requires a Bachelor’s degree in Biological or Physical Sciences and 2+ years of relevant experience in analytical method development,

Qualifications

• Bachelor's degree in Biological or Physical Sciences
• 2+ years of relevant experience with analytical method development
• Experience with ELISA, Cell-Based Assays, HPLC, CE, iCIEF, PCR, SDS-PAGE

Responsibilities

• Perform lab tasks to support development, optimization, validation, and routine testing of protein therapeutics using characterization techniques
• Demonstrate proficiency in ELISA, Cell-Based Assays, HPLC, CE, iCIEF, PCR, SDS-PAGE
• Document method development and validation activities according to current practices
• Assist in training analysts and transfer methods to cGMP QC lab as needed
• Work in a fast-paced team environment, meet deadlines, and prioritize work
• Provide regular updates to Process Development and other teams

Job description

We're Hiring: Research Associate, Analytical Development

Are you an experienced biologics manufacturing professional looking to contribute to the development of life-saving therapies?

Join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals. We are seeking a talented Research Associate to join our Analytical Development team, focusing on innovative analytical methodologies for protein biologics. In this role, you will work closely with experienced scientists to identify and characterize protein biologics, develop methods such as Cell-based, ELISA, HPLC, CE, PCR, and/or SDS-PAGE, and collaborate with Quality Control for method transfer to cGMP testing.

What We're Looking For

Bachelor’s degree in Biological or Physical Sciences

2+ years of relevant xperience with analytical method development using bioanalytical techniques.

- Experience with at least one of the following: ELISA, Cell-Based Assays, HPLC, CE, iCIEF, PCR, SDS-PAGE.

Preferred Qualifications:

• - Experience in assay validation/qualification and knowledge of industry regulations are a plus.

What You'll Do

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

Be part of a team working at the forefront of biopharmaceutical manufacturing and viral vector production, while helping bring innovative therapies closer to patients.

Work Authorization:

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time