Quality Control Senior Associate

amgen· 1061 Amgen Technology (Ireland) UC
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📍 Ireland - DublinFull time

About this role

Career Category

Quality

Job Description

Job Summary: QC CAS - Sr Associate

Under minimal supervision, responsible for one or more of the following activities in QC including analytical testing of Commercial, Stability, Utilities, raw materials and Validation.

  • Contributes to team by ensuring the quality of the tasks/services provided by self

  • Contributes to the completion of Milestones associated with specific projects or activities within team

  • Strives to complete activities right first time

Extended hours and weekend work flexibility may be necessary as required.

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Specific Job Duties:

  • Plan and perform analyses with great efficiency and accuracy.

  • Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.

  • Report, evaluate, back-up/archive, trend and approve analytical data.

  • Troubleshoot, solve problems and communicate with stakeholders.

  • Initiate and/or implement changes in controlled documents.

  • Participate in audits, initiatives and projects that may be departmental or organizational in scope.

  • Review protocols and perform assay validation and equipment qualification/ verifications when required.

  • Introduce new techniques to the lab, including method transfers, reports, validations and protocols.

  • May contribute to regulatory filings.

  • May conduct lab investigations as necessary.

  • Evaluate lab practices for compliance on a continuous basis.

  • Approve lab results.

  • May interact with outside resources.

  • LIMS data coordination of commercial and import testing on site where applicable

  • May represent the department/organization on various teams.

  • May train others.

Primary Knowledge, Skills, Competencies and Relevant Experience

Knowledge:

  • Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.  Deepens technical knowledge through exposure & continuous learning

  • Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery

Skills:

  • Communication skills (verbal and written) at all levels

  • Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)

  • Presentation skills

  • Escalate issues professionally and on a timely basis

  • Decision Making skills

  • Teamwork and Coaching others

  • Negotiation and Influence skills

  • Investigation skills

  • Problem solving skills. Applies research, information gathering, analytical, and interpretation skills to problems of diverse scope

  • Ensures compliance within regulatory environment

  • Develops solutions to technical problems of moderate complexity

  • Screens, categorizes, evaluates, reconciles, reports, and resolves data integrity issues

  • Interprets generally defined practices and methods

  • Able to use statistical analysis tools to perform data trending and evaluation

  • Project Management and organizational skills, including ability to follow assignments through to completion

Competencies:

  • Demonstrated ability to work independently and deliver right first time results

  •  Works under minimal direction Work is guided by objectives of the department or assignment

  • Follows procedures

  • Refers to technical standards, principles, theories and precedents as needed

  • May set project timeframes and priorities based on project objectives and ongoing assignments

  • Recognizes and escalates problems

  • Working knowledge of aseptic compliance within the manufacturing environment and demonstrated leadership and communication skills to communicate requirements to colleagues

  • Auditing documentation and operation process

  • Demonstrated ability to interact with regulatory agencies

Relevant experience:

  • Bachelor’s degree in a Science related field is required. 

  • 4+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry,

  • Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.

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Salary Range

52,756.95 EUR - 71,377.05 EUR

Frequently Asked Questions

Is the salary disclosed for the Quality Control Senior Associate position at amgen?
The salary for this Quality Control Senior Associate role at amgen is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Quality Control Senior Associate position at amgen located?
This Quality Control Senior Associate role at amgen is based in Ireland - Dublin. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Quality Control Senior Associate role at amgen full-time or part-time?
This is listed as a Full time position. It is posted as a Quality Control Senior Associate role in the 1061 Amgen Technology (Ireland) UC department at amgen.
Which team or department does the Quality Control Senior Associate at amgen belong to?
This Quality Control Senior Associate position is part of the 1061 Amgen Technology (Ireland) UC department at amgen. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Quality Control Senior Associate position at amgen?
Click the "Apply Now" button on this page. You will be redirected to amgen's official application portal hosted on workday where you can submit your application directly.
When was the Quality Control Senior Associate job at amgen posted?
This Quality Control Senior Associate position at amgen was posted on Sep 22, 2026. Apply as soon as possible — early applications are often reviewed first.
Quality Control Senior Associate
amgen
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