Find Control laboratory Jobs in Dublin, D

Senior Associate QC (24 / 7 Shift)
Amgen —Dún Laoghaire, County Dublin
- €52,756.95–€71,377.05 a year
- Research
- Analysis skills
- Project management
2d
QA Validation Engineer
CAI —Dublin, County Dublin
- Full-time
- Engineering
- Communication skills
Quick apply
10d
Manager Corporate Drug Regulatory Affairs (12 month agency contract)
Viatris —Northern Cross, County Dublin
- Full-time
- English
- Bachelor's degree
- Communication skills
Design Assurance Engineer, Device Technical Operations ( 18 Months FTC )
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- No degree
- Communication skills
Operations Technician
Charles River Laboratories —Dublin, County Dublin
- Full-time
- Sales
- Microsoft Office
- No degree
- Annual leave
Warehouse Operator
Charles River Laboratories —Dublin, County Dublin
- Full-time
- Leaving certificate
- No degree
- Organisational skills
- Annual leave
- Employee discount
Statutory Accountant
Abbott Laboratories —Dublin, County Dublin
- Full-time
- Accounting
- Accounting
2d
Principal Consultant - Regulatory Affairs
NNIT A/S —Dublin, County Dublin
- Spanish
- Sales
- English
Radiopharmacy Quality Control Radiochemist
Alliance Medical —Dublin, County Dublin
- Full-time
Quick apply
Senior Manager, Quality Assurance - GxP
PTC Therapeutics International Limited —DUBLIN 2, County Dublin
- Full-time
- Microsoft Office
- Bachelor's degree
- Mentoring
Quick apply
Senior Specialist Regulatory Operations (Electronic Submissions)
Viatris —Northern Cross, County Dublin
- Full-time
- Marketing
- English
- Microsoft Office
- Employee assistance program
Senior Quality System Specialist (Maternity leave cover) Remote / Home Based
Jazz Pharmaceuticals —Dublin, County Dublin
- Engineering
- Bachelor's degree
- Continuous improvement
- Annual leave
6d
Senior Risk Management Engineer / Scientist
Viatris —Northern Cross, County Dublin
- Full-time
- Analysis skills
- Communication skills
EHS Associate Manager
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Communication skills
Network Engineer
Abbott Laboratories —Dublin, County Dublin
- Full-time
- Computer Science
- Bachelor's degree
- No degree
10d
Proposal Coordinator-Administrator
DPS Group —Dublin, County Dublin
- Monday to Friday
IT Solutions Leader for Clinical Diagnostics Ireland and UK
Eurofins —Dublin, County Dublin
- Full-time
- Hybrid work
- Azure
- English
- Master's degree
Quick apply
Senior Specialist Device Technical Regulatory
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- English
- Master's degree
Senior Specialist, Equipment and Systems Team (12 months fixed term)
AstraZeneca —Dublin, County Dublin
- Engineering
- AI
- Time management
5d
Principal Data Product Engineer — Data Ontology & Metadata
AstraZeneca —Dublin, County Dublin
- Doctoral degree
- Computer Science
- Master's degree
11d

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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

control laboratory jobs in dublin, d

Senior Associate QC (24 / 7 Shift)

QA Validation Engineer

Manager Corporate Drug Regulatory Affairs (12 month agency contract)

Design Assurance Engineer, Device Technical Operations ( 18 Months FTC )

Operations Technician

Warehouse Operator

Statutory Accountant

Principal Consultant - Regulatory Affairs

Radiopharmacy Quality Control Radiochemist

Senior Manager, Quality Assurance - GxP

Senior Specialist Regulatory Operations (Electronic Submissions)

Senior Quality System Specialist (Maternity leave cover) Remote / Home Based

Senior Risk Management Engineer / Scientist

EHS Associate Manager

Network Engineer

Proposal Coordinator-Administrator

IT Solutions Leader for Clinical Diagnostics Ireland and UK

Senior Specialist Device Technical Regulatory

Senior Specialist, Equipment and Systems Team (12 months fixed term)

Principal Data Product Engineer — Data Ontology & Metadata

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