Find Pharmaceutical shift Jobs in North Dublin County Dublin

Bioprocess Operator @ VLE Therapeutics
APC Ltd —Dublin, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Process Technician (11-Month Contract)
Pfizer —Dublin, County Dublin
- Full-time
- Leaving certificate
- No degree
- Manufacturing
Control Room Operator
BidvestNoonan —Swords, County Dublin
- €17.50 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee assistance program
Quick apply
14d
QA Specialist (Extended Days)
Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
- Engineering
- English
- Communication skills
9d
Assoc. Spclst, Quality Control
MSD —Dunboyne, County Meath
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Analysis skills
10d
Experienced Manufacturing Technician
Intel —Leixlip, County Kildare
- €39,800–€62,200 a year
- Full-time
- Engineering
- Maintenance
- Analysis skills
QA Specialist (Extended Days)
AstraZeneca —Dublin, County Dublin
- Engineering
- English
- Communication skills
9d
QA Validation Manager - FTC
DHL Supply Chain —Swords, County Dublin
- Monday to Friday
- Microsoft Office
- No degree
- Business
- Free parking
- Annual leave
Operations Specialist II (API Manufacturing)
Mallinckrodt —Dublin, County Dublin
- €39,500–€59,500 a year
- Full-time
- Continuous improvement
- Communication skills
Microbiology Technical Specialist (Shift)
MSD —Dunboyne, County Meath
- Full-time
- Hybrid work
- Supervising experience
- Project management
- Bachelor's degree
6d
Manufacturing Supervisor
AbbVie —Dublin, County Dublin
- Full-time
- Engineering
- Supervising experience
- Bachelor's degree
- Free parking
GCP Compliance Manager - Clinical Programs & Trials
Novartis —Dublin, County Dublin
- €75,880–€140,920 a year
- Full-time
- Hybrid work
- Engineering
- Communication skills
Hybrid cleaning supervisor
Sodexo —Dublin, County Dublin
- €18 an hour
- 12 hour shift
- Customer service
- Organisational skills
- In-person
- Free parking
- Employee assistance program
Quick apply
7d
Production Radiochemist
Curium Pharma —Blackrock, County Dublin
- No degree
- Communication skills
2d
Defect Reduction Engineer
Intel —Leixlip, County Kildare
- €59,200–€111,300 a year
- Full-time
- Engineering
- Data analysis skills
- Research
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
Staff Quality Engineer II
BD —Dublin, County Dublin
- €75,900–€115,725 a year
- Engineering
- Analysis skills
- Project management
Engineering Technician ( 12 Months Agency Contract )
Viatris —Damastown, County Dublin
- Full-time
- Continuous improvement
- Manufacturing
QA Team Lead - Shop Floor & Environmental Monitoring (EM)
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- English
- Mentoring
- Manufacturing
Integrated Insights Manager, Execution Excellence
Novartis —Dublin, County Dublin
- €60,830–€112,970 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Doctoral degree
- English

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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 jobs in north dublin county dublin

Bioprocess Operator @ VLE Therapeutics

Process Technician (11-Month Contract)

Control Room Operator

QA Specialist (Extended Days)

Assoc. Spclst, Quality Control

Experienced Manufacturing Technician

QA Specialist (Extended Days)

QA Validation Manager - FTC

Operations Specialist II (API Manufacturing)

Microbiology Technical Specialist (Shift)

Manufacturing Supervisor

GCP Compliance Manager - Clinical Programs & Trials

Hybrid cleaning supervisor

Production Radiochemist

Defect Reduction Engineer

Senior Scientific Engagement & Program Manager

Staff Quality Engineer II

Engineering Technician ( 12 Months Agency Contract )

QA Team Lead - Shop Floor & Environmental Monitoring (EM)

Integrated Insights Manager, Execution Excellence

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