Find Process science shift 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
Associate Analyst, Pricing
Analog Devices —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Microsoft Access
- ERP systems
4d
Clinical Study Data Lead - Dublin
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Mentoring
2d
Clinical Data Analytics Lead
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- English
- Python
Automation QA Engineer
StoneX Group —Dublin, County Dublin
- Azure
- Computer Science
- English
11d
PM2 Manufacturing Manager (Days)
Amgen —Dún Laoghaire, County Dublin
- €78,613.10–€106,358.90 a year
- Engineering
- English
- Bachelor's degree
9d
Special Care Worker – Special Care Setting – Youth Based Residential
MCMA —DUBLIN 22, County Dublin
- Full-time
- Bachelor's degree
- No degree
- Recruiting
- Annual leave
- Referral programme
Quick apply
International HEOR & HTA Associate Director, NS
Novartis —Dublin, County Dublin
- €84,630–€157,170 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Research
11d
Global Labelling Associate Director, Content (Established Products)
Novartis —Dublin, County Dublin
- €75,880–€140,920 a year
- Full-time
- Hybrid work
- Continuous improvement
Architect - Automation N 4D
Genpact Ireland Private Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Computer Science
- English
- Master's degree
Quick apply
6d
Engineering Shift Technician
Embecta —Dún Laoghaire, County Dublin
- 12 hour shift
- Engineering
- Analysis skills
- Continuous improvement
Principal Cybersecurity Data Engineer
Workday —Dublin, County Dublin
- €104,000–€156,000 a year
- Full-time
- Master's degree
- SQL
- AWS
2d
Global Labelling Associate Director, Content (Oncology)
Novartis —Dublin, County Dublin
- €75,880–€140,920 a year
- Full-time
- Hybrid work
- Continuous improvement
Director Global Costing Center of Excellence
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- ERP systems
- Finance
Senior Software Development Engineer in Test
PlayStation Global —Dublin, County Dublin
- €72,700–€109,100 a year
- Computer Science
- DevOps
- Java
Quick apply
TFSM IR EHS Safety and Industrial Hygiene Engineer
Intel —Leixlip, County Kildare
- €59,200–€111,300 a year
- Full-time
- Microsoft Excel
- Engineering
- Analysis skills
Senior QA Automation Engineer (AI-First)
Storyful —Dublin, County Dublin
- Full-time
- Master's degree
- SQL
- AWS
Senior Scientific Engagement & Program Manager
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
4d
Head of Data Governance, Anonymization and Quality
Novartis —Dublin, County Dublin
- €90,300–€167,700 a year
- Full-time
- Doctoral degree
- Computer Science
- Research
Global Labelling Director, Content
Novartis —Dublin, County Dublin
- €90,300–€167,700 a year
- Full-time
- Hybrid work
- Leadership

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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

process science shift jobs in dublin, d

Senior Associate QC (24 / 7 Shift)

Associate Analyst, Pricing

Clinical Study Data Lead - Dublin

Clinical Data Analytics Lead

Automation QA Engineer

PM2 Manufacturing Manager (Days)

Special Care Worker – Special Care Setting – Youth Based Residential

International HEOR & HTA Associate Director, NS

Global Labelling Associate Director, Content (Established Products)

Architect - Automation N 4D

Engineering Shift Technician

Principal Cybersecurity Data Engineer

Global Labelling Associate Director, Content (Oncology)

Director Global Costing Center of Excellence

Senior Software Development Engineer in Test

TFSM IR EHS Safety and Industrial Hygiene Engineer

Senior QA Automation Engineer (AI-First)

Senior Scientific Engagement & Program Manager

Head of Data Governance, Anonymization and Quality

Global Labelling Director, Content

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