Sr. Research Associate, Analytical Development

avidbio; Tustin (CA); On-site; USD 84,000 - 105,000; Full time

Benefits offered by this job

Health insurance

401(k) matching

Paid time off

Job summary

Avidbio is seeking a Sr. Research Associate in Analytical Development to join a dedicated team developing life-saving biopharmaceuticals. This full-time role involves developing methods for protein biologics and working alongside experienced professionals to ensure quality and efficiency.

The ideal candidate should have significant industry experience in analytical methods, including HPLC and ELISA. A supportive work environment is offered, along with competitive compensation and growth opportunities.

Qualifications

• 4+ years of QC or Analytical lab experience with a BS degree.
• 2+ years of QC or Analytical lab experience with a MS degree.
• Familiarity with GMPs and regulatory audits.

Responsibilities

• Perform routine wet chemistry assays and ELISA/cell-based immunoassays.
• Develop, review, and write test methods and standard operating procedures.
• Support continuous improvement initiatives.

Skills

Analytical testing

HPLC experience

Protein characterization

Electrophoresis

Assay validation

Education

BS in Biochemistry, Chemistry, Biology or Pharmaceutical Sciences

MS in relevant field (alternative)

Tools

Octet

Liquid handler

Maurice

Job description

Looking to join a passionate team dedicated to developing and manufacturing life‑saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.

Your Role:

Are you an experienced Sr. Research Associate, Analytical Development looking to take the next step in your career? We’re seeking a talented and passionate individual to join our Analytical Development team as we develop cutting‑edge protein biologics. As our Sr. Research Associate, you’ll focus on developing Cell‑based, ELISA, HPLC, CE, PCR and/or SDS‑PAGE methods, while working alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. This position offers the chance to interface with our Quality Control testing group as methods are transferred into that group for cGMP testing, and you may also have the opportunity to interface with external clients.

Key Responsibilities:

• Perform and review routine wet chemistry assays and ELISA/cell‑based immunoassays, electrophoresis (SDS‑PAGE/IEF) and HPLC.
• May train/supervise the experimental work of more junior analysts and may be a member of inter‑departmental/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.
• Previous experience in either HPLC/CE or potency/ELISA assay methodologies is required.
• Knowledgeable of company cGMPs as well as industry regulations that apply to job functions. Participates in regulatory inspections.
• Support continuous improvement initiatives.
• Other duties as assigned.

Minimum Qualifications:

• 4+ years industry experience working in a QC or Analytical lab (with a BS degree) preferably Biochemistry, Chemistry, Biology or pharmaceutical sciences.
• 2+ years industry experience working in a QC or Analytical lab (with a MS degree).
• Analytical testing and equipment utilizing analytical biochemistry methods.
• Writing reports/procedures/specifications.
• GMPs and regulatory audits.
• Potency/ELISA and/or HPLC experience is essential.
• Should also have experience with most if not all the following: protein characterization, electrophoresis, chromatography, and assay validation/qualification.

Preferred Qualifications:

• Experience with Octet, liquid handler and Maurice is a plus!

Position Type/Expected Hours of Work:

This role is a full‑time position operating Monday through Friday, unless otherwise stated by Supervisor. Any scientific staff member can expect to work overtime, including during the weekends. Off‑site meetings with clients and regulatory agencies are a usual occurrence.

Compensation:

We offer competitive compensation packages for this role, including a base salary, performance‑based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $84,000 - $105,000 annually, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.

Who you are:

• You have a “bring it on!” team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
• Your written and verbal skills are of a high standard, and you communicate with clarity and confidence.
• You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
• You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:

In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day‑to‑day demands of this position.