Amgen

Pharmaceuticals

SeniorAssociate-QCTechnicalServices

Ireland FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“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.

Pharmaceuticals
Problems you'll solve

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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