Manufacturing Associate - Hybrid/Remote Biotech Ops

BioSpace; Thousand Oaks (CA); On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Competitive benefits

Remote/hybrid options

Career development

Job summary

Amgen in Thousand Oaks is seeking an Associate Manufacturing to work across QA, QC, Engineering, and Facilities. You will gain deep insight into manufacturing operations and planning, performing formulation activities and batch record reviews to ensure quality and compliance.

The role emphasizes cross-functional collaboration and data-driven improvements. The ideal candidate will have GMP experience, be proficient with MS Office/Excel, and be prepared to work in a dynamic, regulated environment.

Qualifications

• High school/GED plus 2 years Manufacturing experience or
• Associates plus 6 months Manufacturing experience or
• Bachelor's degree required or equivalent

Responsibilities

• Execute drug product formulation activities
• Perform initial review of manufacturing batch records
• Maintain safe and compliant culture by identifying preventative measures
• Create and/or revise standard operating procedures
• Lead continuous improvement initiatives, cross-functional
• Perform data analysis (SPC, CPV) of process parameters
• Develop finite schedule for unit operations
• Monitor productivity and address cycle time issues
• Escalate critical events to management
• Perform cleaning/sanitization of manufacturing areas and equipment
• Utilize systems (SAP, QMTS, LIMS)
• Support introduction of new products/technologies
• Initiate and own quality records (NC, CAPA)

Skills

MS Office

Excel

Regulatory compliance

Quality Assurance

Quality Control

Education

High school/GED

Associates

Bachelor's

B.S. in life science

Tools

SAP

QMTS

LIMS

Job description

Amgen in Thousand Oaks is seeking an Associate Manufacturing to work across QA, QC, Engineering, and Facilities. You will gain deep insight into manufacturing operations and planning, performing formulation activities and batch record reviews to ensure quality and compliance.

The role emphasizes cross-functional collaboration and data-driven improvements. The ideal candidate will have GMP experience, be proficient with MS Office/Excel, and be prepared to work in a dynamic, regulated environment.