MCS Manufacturing Associate
BioSpace, Thousand Oaks, CA, United States
Associate Manufacturing
What You Will Do
In this vital role, you will work in a dynamic production environment at the Amgen Thousand Oaks Drug Product Packaging & Assembly plant supporting flexible and agile device assembly and packaging organization. You will support the production of drug product packaging and assembly activities for clinical trials worldwide, assisting in device development testing and performing semi-complex manufacturing operations under general supervision.
Executing drug‑product packaging and assembly activities.
Support planning and organization (time, staff, lines, materials, equipment).
Organize and lead team meetings.
Support problem‑solving sessions by serving as SME as needed.
Divide work, providing clear guidance and instructions to the team.
Drive continuous improvement with the team and act as coach for production activities.
Collaborate with Line Owner and FLM on process equipment investigations.
Fill gaps in the production lines and support as required.
Perform initial reviews of manufacturing batch records.
Maintain a safe environment while adhering to compliance standards, identifying preventive measures.
Craft and/or revise standard procedures.
Elevate critical and impactful events to management.
Utilize appropriate systems (SAP, MES, QMTS, LIMS, etc.).
Provide SME support to Line Owners and NPI leads as needed.
Initiate quality records and support triage.
Assemble combination products such as Auto Injectors and Automated Mini Dosers using semi‑automated equipment.
Bottle small‑molecule tablets via manual or automated processes.
Assemble vial sleeves, label, and package –70‑degree C products.
Basic Qualifications
High school/GED + 2 years manufacturing or military experience.
Associate degree + 6 months manufacturing or military experience.
Bachelor’s degree preferred.
Preferred Qualifications
Knowledge of CFR and regulatory requirements.
Mechanical aptitude.
Knowledge of WIP lab equipment and computer systems.
Basic statistical/mathematical skills.
Ability to interpret and apply GMP knowledge.
Understanding of analytical methods for manufacturing.
Basic troubleshooting skills for purification equipment.
Excellent written and verbal communication skills.
Ability to prioritize tasks and work in a challenging, fast‑paced environment.
Benefits
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
A discretionary annual bonus program.
Stock‑based long‑term incentives.
Award‑winning time‑off plans.
Flexible work models, including remote and hybrid arrangements where possible.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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What You Will Do
In this vital role, you will work in a dynamic production environment at the Amgen Thousand Oaks Drug Product Packaging & Assembly plant supporting flexible and agile device assembly and packaging organization. You will support the production of drug product packaging and assembly activities for clinical trials worldwide, assisting in device development testing and performing semi-complex manufacturing operations under general supervision.
Executing drug‑product packaging and assembly activities.
Support planning and organization (time, staff, lines, materials, equipment).
Organize and lead team meetings.
Support problem‑solving sessions by serving as SME as needed.
Divide work, providing clear guidance and instructions to the team.
Drive continuous improvement with the team and act as coach for production activities.
Collaborate with Line Owner and FLM on process equipment investigations.
Fill gaps in the production lines and support as required.
Perform initial reviews of manufacturing batch records.
Maintain a safe environment while adhering to compliance standards, identifying preventive measures.
Craft and/or revise standard procedures.
Elevate critical and impactful events to management.
Utilize appropriate systems (SAP, MES, QMTS, LIMS, etc.).
Provide SME support to Line Owners and NPI leads as needed.
Initiate quality records and support triage.
Assemble combination products such as Auto Injectors and Automated Mini Dosers using semi‑automated equipment.
Bottle small‑molecule tablets via manual or automated processes.
Assemble vial sleeves, label, and package –70‑degree C products.
Basic Qualifications
High school/GED + 2 years manufacturing or military experience.
Associate degree + 6 months manufacturing or military experience.
Bachelor’s degree preferred.
Preferred Qualifications
Knowledge of CFR and regulatory requirements.
Mechanical aptitude.
Knowledge of WIP lab equipment and computer systems.
Basic statistical/mathematical skills.
Ability to interpret and apply GMP knowledge.
Understanding of analytical methods for manufacturing.
Basic troubleshooting skills for purification equipment.
Excellent written and verbal communication skills.
Ability to prioritize tasks and work in a challenging, fast‑paced environment.
Benefits
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
A discretionary annual bonus program.
Stock‑based long‑term incentives.
Award‑winning time‑off plans.
Flexible work models, including remote and hybrid arrangements where possible.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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