Associate Manufacturing: GMP Ops & Process Improvement

VetJobs; Thousand Oaks (CA); On-site; USD 71,000 - 96,000; Full time

Benefits offered by this job

Retirement plan

Stock-based incentives

Flexible work models

Job summary

Amgen in Thousand Oaks is seeking an Associate Manufacturing professional to collaborate with Quality Assurance, Quality Control, Engineering and Facilities to learn and optimize manufacturing operations. You will gain hands-on experience across multiple functions and contribute to a high-performing team.

The role involves executing drug product formulation, reviewing batch records, and driving continuous improvement while maintaining compliance.

Qualifications

• High school/GED plus 2 years manufacturing experience, or Associate’s + 6 months manufacturing experience, or Bachelor’s.
• 2 years of work experience in a GMP environment is preferred.
• Ability to perform computer operations with MS Office and Excel; operate specialized equipment as applicable.

Responsibilities

• Executing drug product formulation activities.
• Performing initial review of manufacturing batch records.
• Maintaining a safe and compliant culture by identifying preventative measures.
• Creating and/or revising standard operating procedures.
• Leading continuous improvement initiatives, cross-functional when needed.
• Performing data analysis (e.g., SPC, CPV) and advising Engineering/Process Development teams.
• Developing finite schedule for unit operations.
• Monitoring productivity and addressing issues affecting cycle time.
• Elevating critical events to management.
• Performing cleaning/sanitation of manufacturing areas and equipment as applicable.
• Using SAP, QMTS, and LIMS for job duties.

Skills

MS Office

Excel

GMP experience

Regulatory compliance

Education

Bachelor’s degree

Associate degree

Tools

SAP

QMTS

LIMS

MS Office

Job description

Amgen in Thousand Oaks is seeking an Associate Manufacturing professional to collaborate with Quality Assurance, Quality Control, Engineering and Facilities to learn and optimize manufacturing operations. You will gain hands-on experience across multiple functions and contribute to a high-performing team.

The role involves executing drug product formulation, reviewing batch records, and driving continuous improvement while maintaining compliance.