Find Pharmaceutical shift work Jobs in Dublin, D

Bioprocess Operator @ VLE Therapeutics
APC Ltd —Dublin, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Bioprocess Technician
Amgen —Dún Laoghaire, County Dublin
- €39,477.40–€53,410.60 a year
- Leaving certificate
- No degree
- Manufacturing
Manufacturing Process Technician
Amgen —Dún Laoghaire, County Dublin
- €39,477.40–€53,410.60 a year
- English
- Leaving certificate
- No degree
De- Trashing Technician
Sodexo —Dublin, County Dublin
- €18.22 an hour
- Full-time
- In-person
- Free parking
- Employee assistance program
Quick apply
5d
Operations Specialist II (API Manufacturing)
Mallinckrodt —Dublin, County Dublin
- €39,500–€59,500 a year
- Full-time
- Continuous improvement
- Communication skills
8d
Manufacturing Technologist
Ipsen Manufacturing Ireland Ltd —Dublin, County Dublin
- Full-time
- Bachelor's degree
6d
Critical Environment Technician - Shift 24/7
Microsoft —Dublin, County Dublin
- €52,300–€75,200 a year
- Full-time
- Azure
- Assembly
- No degree
2d
Learning Delivery Manager
Novartis —Dublin, County Dublin
- €57,120–€106,080 a year
- Full-time
- Master's degree
- Bachelor's degree
- Business
General Operative Supervisor
Apleona Ireland —Dublin, County Dublin
- €19–€22 an hour
- Nights as needed
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
Quick apply
3d
Regulatory Affairs Specialist Ireland
Organon —Dublin, County Dublin
- Full-time
- English
- Microsoft Office
- Project management
Quick apply
2h
Sales & Marketing Project Coordinator
Novartis —Dublin, County Dublin
- €31,150–€57,850 a year
- Full-time
- Communication skills
- Marketing
Staff Quality Engineer II
BD —Dublin, County Dublin
- €75,900–€115,725 a year
- Engineering
- Analysis skills
- Project management
6d
Medical Advisor, General & Speciality Medicine
MSD —Leopardstown, County Dublin
- Full-time
- Doctoral degree
- Microsoft Office
- Master's degree
1d
Warehouse Technician
Amgen —Dún Laoghaire, County Dublin
- €39,477.40–€53,410.60 a year
- Day shift
- Writing skills
- Forklift
- Continuous improvement
7d
Manufacturing Supervisor
AbbVie —Dublin, County Dublin
- Full-time
- Engineering
- Supervising experience
- Bachelor's degree
- Free parking
Clinical Document Management Learning Manager
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Research
- Bachelor's degree
- No degree
WPM C4 Ireland Equipment Technician
Intel —Leixlip, County Kildare
- €35,800–€55,900 a year
- Full-time
- Maintenance
- Analysis skills
- Continuous improvement
2d
Experienced Manufacturing Technician
Intel —Leixlip, County Kildare
- €39,800–€62,200 a year
- Full-time
- Engineering
- Maintenance
- Analysis skills
QA Validation Manager - FTC
DHL —Dublin, County Dublin
- Monday to Friday
- Microsoft Office
- No degree
- Business
- Free parking
- Annual leave
9d
Global Labelling Manager, Content (Neuroscience)
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Communication skills

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Bioprocess Operator @ VLE Therapeutics

APC Ltd -
Dublin, County Dublin

Quick apply

Job details

Full-time

Qualifications

Microsoft Word
Microsoft Excel
React
English
Leaving certificate
Data collection
Manufacturing

Full job description

Bioprocessing Operator

About VLE Therapeutics

Powered by transformation research in APC, VLE Therapeutics Ltd was formed to extend the value chain and deliver science and digital led manufacturing of Vaccines and Advanced Therapeutics. VLE Therapeutics will support the GMP manufacturing of clinical and commercial vaccines, next generation biologics advanced therapeutics and aims to transform the time and cost associated to produce medicines for our clients. This will be the first Irish-owned facility expressly designed to provide Ireland and Europe with a local supply chain for these critical medicines.

To create the best client experience, we will create implement a seamless handover process from APC process development into GMP manufacturing, leveraging our novel platforms to deliver a Molecule-2-Market accelerator.

Stage 1- At our current APC facility, we are constructing a new state of the art biomanufacturing facility. Operations will employ cutting edge technology including single use equipment disposables and deploy digital solutions to support the best client experience.

Stage 2- In parallel, we are planning the development of a bespoke 80,000ft2.

greenfield GMP manufacturing facility, which will provide a world-class platform for the manufacture of a wide range of vaccines next generation biologics advanced therapeutics for our clients globally.

Key to enabling our strategy is to create the best culture, the right values behaviours and as a result, the establishment of a high performing team committed to creating a culture of excellence in everything we do.

Position Summary

Principal Responsibilities

Demonstrate high performance behaviours, ability to work collaboratively within a cross functional team, ability to show independent initiative, to have a focus on continuous improvement and have a strong belief in supporting the right culture in the business.
Operate equipment and run processes in a clean room environment, in accordance with batch record, user manuals, design parameters, equipment qualification protocols and validation protocols and current standard GMP operating procedures.
Execution of operational activities for GMP production such as equipment preparation, component cleaning, USP operations (Inoculum, cell culture) and DSP operations (purification, chromatography, Drug Substance Final Fill), Filter Integrity testing and aseptic operations.
Adhere to compliance requirements (safety, quality environmental) and ensure any adverse events are communicated/troubleshot appropriately.
Be capable of understanding and responding appropriately to adverse events. Ability to react appropriately to non-standard events.Troubleshoot equipment issues, when necessary
Monitoring and collecting data (including input to an electronic system) on critical parameters to anticipate potential upsets and notifying supervision/technical support of same. Data is used to identify issues and/or make process improvements.
Process sampling and sample testing with analytical equipment, pH, conductivity, cell counting, environmental monitoring and routine calibration of same.
Receiving and verification of all raw materials. Equipment set-up. Parts preparation. Deactivation of waste i.e., Biowaste system or autoclaves
Logging safety and quality events in the appropriate systems, including initiating process deviations
Completion of all relevant training on associated Individual Training Plans to complete manufacturing activities in a GMP manner.
Support continuous improvement initiatives by identifying areas needing improvement, recommending strategies for improvement, and implementing those strategies once approved.
Collaborate with other departments and represent Manufacturing in cross functional initiatives and meetings.
Maintain good housekeeping and clean and sanitize classified areas as required.

Experience Qualifications

More than 5 years’ experience in cGMP Pharmaceutical Operations is essential.
More than 3 years’ experience in Drug Substance Biologics manufacturing is essential.
Vaccine manufacturing experience is preferable.
Advanced Therapeutics (Cell Gene Therapy) manufacturing experience is a positive.
Aseptic operations experience is preferable.
The role may operate on rotating shift position and may also involve some non-scheduled call-in time to respond to plant emergencies etc. and some scheduled call-in time to attend process operations.
Must be able to read, write and converse in English.
Must have good working knowledge of MS Excel and Word
Ability to work in an intense, fast-paced work environment.
Ability to function, with guidance, in a rapidly changing environment while balancing multiple priorities simultaneously.
Ability to work independently and as part of a team.

Education

Leaving Certificate or equivalent at a minimum. L7 or L8 Degree in a scientific discipline or equivalent experience preferred

How to apply:

Suitable applicants should submit a CV and Cover Letter. Please note that the closing date for applications for this position is 15th June 2026

VLE is committed to the principle of equal opportunity for all employees. All employment decisions at VLE are based on business needs, job requirements and individual qualifications, without regard to gender, ethnicity, age, religious belief, disability, sexual orientation, gender identity and/or expression, marital status, or any other status protected by Irish law.

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Refine Your Search

pharmaceutical shift work jobs in dublin, d

Bioprocess Operator @ VLE Therapeutics

Bioprocess Technician

Manufacturing Process Technician

De- Trashing Technician

Operations Specialist II (API Manufacturing)

Manufacturing Technologist

Critical Environment Technician - Shift 24/7

Learning Delivery Manager

General Operative Supervisor

Regulatory Affairs Specialist Ireland

Sales & Marketing Project Coordinator

Staff Quality Engineer II

Medical Advisor, General & Speciality Medicine

Warehouse Technician

Manufacturing Supervisor

Clinical Document Management Learning Manager

WPM C4 Ireland Equipment Technician

Experienced Manufacturing Technician

QA Validation Manager - FTC

Global Labelling Manager, Content (Neuroscience)

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