In-Process QC Analyst - GMP Analytics

BioMarin Pharmaceutical Inc.; Novato (CA); On-site; USD 65,000 - 90,000; Part time

Job summary

BioMarin Pharmaceutical Inc. is seeking a Quality Control Analytical In-Process (QCA-IP) Analyst for a contract role on a Wednesday–Saturday shift onsite, supporting in-process testing and method validation in accordance with cGMP.

You will perform a range of analytical tests (A280, Bradford, UV, HPLC/UPLC), maintain documentation, and contribute to optimization and investigations while coordinating with manufacturing teams.

Qualifications

• Bachelor of Science degree in a scientific field.
• Good documentation and written/verbal communication skills essential.
• Familiarity with quality systems, cGMP, and QC principles.
• Experience with SAP or similar ERP systems preferred.

Responsibilities

• Timely facilitation of sample receipt and accessioning flow.
• Execute analytical methods for in-process testing under cGMP guidelines.
• Evaluate assay validity, summarize results, and assist trend analysis.
• Share housekeeping activities and maintain lab readiness.
• Monitor and control laboratory supplies and reagents.
• Provide training on methods to less experienced staff.
• Report compliance risks and deviations; initiate investigations.
• Support method validation and transfer protocols.
• Attend team meetings and suggest improvements.
• Identify opportunities to improve operational efficiency and reduce waste.

Skills

Written and verbal communication

Good documentation

Laboratory skills

Education

Bachelor of Science degree

Tools

SAP

BINOCS

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

BioMarin Pharmaceutical Inc. is seeking a Quality Control Analytical In-Process (QCA-IP) Analyst for a contract role on a Wednesday–Saturday shift onsite, supporting in-process testing and method validation in accordance with cGMP.

You will perform a range of analytical tests (A280, Bradford, UV, HPLC/UPLC), maintain documentation, and contribute to optimization and investigations while coordinating with manufacturing teams.