Amgen
Pharmaceuticals
SeniorAssociate-QCTechnicalServices
Neural analysis suggests this role is
optimal for Senior candidates.
“Senior Associate - QC Technical Services at Amgen. Skills: Equipment Qualification, Calibration, Maintenance, Data Integrity. Plan qualification, calibration, maintenance of laboratory systems. Manage calibration technician schedules”
What You'll Achieve.
Ensure Quality; Be Science Based; Be Accountable
Industry & Context.
Conduct impact assessments/investigations
What They're Looking For.
Must Have
5 + years of laboratory experience in a cGXP laboratory environment, Exposure to analytical instrument validation, Knowledge of methodology and instrumentation and analytical techniques used for biopharmaceutical testing, Understanding of current regulatory requirements for cGXP laboratory equipment validation and electronic record integrity
Nice to Have
Demonstrated success in managing an equipment qualification or maintenance program
What You'll Do.
maintenance of laboratory systems
Manage calibration technician schedules
Track maintenance and calibration activities
Author/own/approve validation documents
Perform Data Integrity testing
Manage QC equipment lifecycle
Select and procure laboratory equipment
Project manage change controls
Develop qualification project plans
Generate and resolve deviations
Write operating procedures and manuals
Design and conduct training
Develop Data Integrity Assessments
Conduct periodic reviews
Manage equipment replacement
Support safety investigations
Develop maintenance and calibration programmes
Perform assessment of pharmacopeia updates
Conduct routine calibration
Coordinate equipment repairs
Improve equipment performance
Assess equipment failures
Serve as vendor contact
Review calibration and maintenance documentation
Coordinate vendor audits
Support equipment deviations and investigations
Defend validation philosophy in audits
Contribute to continuous improvement
Participate in technical project teams
Support Global System Lifecycle management
Support laboratory investigations
How You'll Work.
Team & Collaboration
Contribute to team training and mentoring; Act as system owner; Participate in technical project teams; Support Global/ Enterprise System Lifecycle management
Communication Scope
Communicate
Process & Methodology
Project manages change controls, Develop equipment qualification project plan
Full Job Description
## **Career Category** Quality ## ## **Job Description** **Level 4 -** Job Description - **Amgen Dun Laoghaire - Dublin** **System Owner – F &E Senior Associate – QC Equipment Support** **Overview:** Supporting the technical services team, the Senior Associate is responsible for planning, executing and documenting the qualification, calibration and routine maintenance of laboratory systems for cGMP Quality Control laboratory facilities at Amgen Dun Laoghaire. Responsible for managing & coordinating the schedules of Calibration Technicians & ensuring that all maintenance & calibration activities are tracked & managed through the Computerized Maintenance Management System (CMMS) Maximo. Responsible for authoring/owning and approving Validation Life Cycle documents for computer related systems including responsibility for Data Integrity testing and business administration of Laboratory Computer Related systems. The Senior Associate will act as system owner in the technical services team and will contribute to team training and mentoring. **Key Responsibilities** Supporting the Quality Control Laboratories, the System Owner is responsible for the complete life cycle of QC equipment. Responsibilities include Equipment Lifecyle management * Select and procure laboratory equipment in accordance with Amgen requirements. * Owns and project manages change controls and adhere to Change Control metrics. * Planning, executing and documenting the qualification of new laboratory equipment in a cGxP regulated environment. * Developing and maintaining an equipment qualification project plan, requirements, qualification protocols and summary reports as part of the commissioning of new laboratory equipment. * Generation and resolution of protocol deviations as required. * Writing/contributing to equipment operating procedures and manuals. * Designing and conducting training for QC staff, and other department staff as applicable. * Developing and maintaining Data Integrity Assessments
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