In-Process QC Analyst — Biotech GMP Impact

Avid Bioservices; Tustin (CA); On-site; USD 35,500 - 44,372; Full time

Job summary

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

The role involves testing, buffer formulation, method writing, aseptic sampling and data reporting, with collaboration across departments to ensure compliance and successful lot release. This full-time position offers competitive pay and benefits within a leading biopharma CDMO.

Qualifications

• Bachelor's degree or 2–4+ years of biotech QC/analytical lab experience.
• Experience with analytical testing, writing reports, GMPs, and regulatory audits.
• Experience with most listed methodologies.
• Experience with maintenance and troubleshooting of analytical instrumentation.

Responsibilities

• Perform basic compendial test methods following written protocols.
• Formulate buffers and reagents for test methods.
• Write and revise test methods and procedures.
• Perform aseptic sampling, endotoxin, pH, conductivity, osmolality, A280 and endotoxin by LAL.
• Perform water testing and raw material sampling and testing.
• QC testing for lot release, development/validation projects, and investigations.
• Draft study protocols and reports.
• Collaborate with other departments to update QC procedures.
• Aware of cGMPs and applicable regulations.
• Handle sample pick up and locating per protocols.

Skills

GMP knowledge

Regulatory audits

Data analysis

Technical writing

Attention to detail

Team collaboration

Education

Bachelor's degree

Tools

Analytical instrumentation

Job description

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

The role involves testing, buffer formulation, method writing, aseptic sampling and data reporting, with collaboration across departments to ensure compliance and successful lot release. This full-time position offers competitive pay and benefits within a leading biopharma CDMO.