QC In-Process Analyst - Biopharma GMP Testing

avidbio; Tustin (CA); On-site; USD 73,897,000 - 92,295,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

401(k) matching

Paid time off

Job summary

Avid Bioservices in California is seeking a Quality Control In-Process Analyst to support manufacturing, validation, process development and stability studies in a GMP environment.

You will perform testing and sampling, write methods and reports, and collaborate across departments to uphold cGMPs while contributing to lot release and investigations. This is a full-time role with a 4x10 schedule and competitive benefits.

Qualifications

• Experience with analytical testing, writing reports, GMPs and regulatory audits.
• Experience with most methodologies listed in QC In-Process testing.
• Maintenance and troubleshooting of analytical instrumentation is desirable.

Responsibilities

• Perform basic compendial test methods and analyze data.
• Formulate buffers and reagents for test methods.
• Write and revise test methods and procedures.
• Perform aseptic sampling, endotoxin, pH, conductivity, osmolality, A280 and LAL.

Skills

Biotech experience

Analytical testing

Documentation/report writing

Education

Bachelor’s degree or 2-4+ years biotech experience

Tools

Analytical instrumentation

Job description

Avid Bioservices in California is seeking a Quality Control In-Process Analyst to support manufacturing, validation, process development and stability studies in a GMP environment.

You will perform testing and sampling, write methods and reports, and collaborate across departments to uphold cGMPs while contributing to lot release and investigations. This is a full-time role with a 4x10 schedule and competitive benefits.