Find Ii, aurora control plane developer Jobs in Dublin, D

Senior Associate QC (24 / 7 Shift)
Amgen —Dún Laoghaire, County Dublin
- €52,756.95–€71,377.05 a year
- Research
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- Part-time
- Microsoft Word
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Bank of Ireland —Dublin, County Dublin
- Full-time
- Hybrid work
- No degree
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- Annual leave
- Employee assistance program
Laboratory Support Coordinator
ICON Plc —Dublin, County Dublin
- Full-time
5d
First Line of Defence - 1LOD - Risk Assurance Senior Associate
Davy —Dublin, County Dublin
- Hybrid work
- Microsoft Powerpoint
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- Project management
- Employee assistance program
Quick apply
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RCPI —DUBLIN 2, County Dublin
- Leadership
- Communication skills
- Office experience
Quick apply
5d
Compliance Monitoring Senior Associate
Davy —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Excel
- Master's degree
- IT
- Employee assistance program
Quick apply
2d
Director, Fund Oversight
HarbourVest Partners —Dublin, County Dublin
- Full-time
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4d
Project Manager
Codec —Dublin, County Dublin
- Full-time
- Hybrid work
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Quick apply
Senior Field Service Engineer
Hitachi —Leixlip, County Kildare
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Senior Field Service Engineer
Hitachi Rail —Leixlip, County Kildare
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Engineer II, Field Service
ASM International —Lucan, County Dublin
- Full-time
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Senior Actuary
Artex —DUBLIN 2, County Dublin
- Full-time
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Overhead Line Network Designer
TLI Group Ltd —Dublin, County Dublin
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Actuarial Manager
Canada Life Group Services —Dublin, County Dublin
- No degree
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10d
SoC Validation/FPGA Engineer (Senior Engineer II)
Microchip Technology —Dublin, County Dublin
- Full-time
- C++
- Bachelor's degree
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Driver / Warehouse Operative
Kellihers —Dublin, County Dublin
- Full-time
- Analysis skills
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- Warehouse experience
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Senior Associate QC (24 / 7 Shift)

Amgen -
Dún Laoghaire, County Dublin

Apply Now

Job details

€52,756.95–€71,377.05 a year
2 days ago

Qualifications

Research
Analysis skills
Project management
Bachelor's degree
Quality control
Technical writing
Leadership
Communication skills
Negotiation

Full job description

Ireland - Dun Laoghaire

JOB ID: R-250127 LOCATION: Ireland - Dun Laoghaire WORK LOCATION TYPE: On Site DATE POSTED: Jul. 31, 2026 CATEGORY: Quality SALARY RANGE: 52,756.95 EUR - 71,377.05 EUR

Senior Associate QC Analytics - Overview:

Under minimal supervision, responsible for one or more of the following activities in QC including HPLC, CE, GELs, analytical testing, characterization, method transfer, sample and data management and equipment maintenance.

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

This role will support manufacturing operations, as such work will be as part of a 24/7 shift pattern and flexibility may be necessary.

.

Specific Job Duties:

With a high degree of technical flexibility, work across diverse areas within the lab.
Plan and perform routine analyses with 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.
Write protocols and perform assay validation and equipment qualification/ verification.
Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.
Approve lab results.
May participate in lab investigations.
May provide technical guidance.
May train others.
May contribute to regulatory filings.
May represent the department/organization on various teams.
May interact with outside resources.

Knowledge:

Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning
Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery
Experience in a wide variety of analytical techniques including but not limited to HPLC, Capillary Electrophoresis, UV and density testing.

Skills:

Take initiative to identify and drive improvements.
Excellent verbal and written communication skills.

a. Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)
b. Presentation skills.
c. Escalate issues professionally and on a timely basis.

Decision Making skills.
Teamwork and Coaching others.
Negotiation and Influence skills.
Problem solving skills.

a. Applies research, information gathering, analytical, and interpretation skills to problems of diverse scope
i. Ensures compliance within regulatory environment
ii. Develops solutions to technical problems of moderate complexity
iii. Screens, categorizes, evaluates, reconciles, reports, and resolves data integrity issues
b. Interprets generally defined practices and methods
c. 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

Compentencies:

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

a. Works under minimal direction
b. Work is guided by objectives of the department or assignment
i. Follows procedures
ii. Refers to technical standards, principles, theories and precedents as needed
iii. May set project timeframes and priorities based on project objectives and ongoing assignments
iv. Recognizes and escalates problems

Demonstrated leadership and communication skills
Auditing documentation and operation process
Demonstrated ability to interact with regulatory agencies

Relevant experience:

Bachelor’s degree in a science discipline.
5+ 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 GMP manufacturing and testing of pharmaceutical products.

Apply Now

Refine Your Search

ii, aurora control plane developer jobs in dublin, d

Senior Associate QC (24 / 7 Shift)

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Senior Actuary

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Actuarial Manager

SoC Validation/FPGA Engineer (Senior Engineer II)

Driver / Warehouse Operative

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