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 Europewith 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
A key member in supporting the execution of cGMP operational activities in VLE Therapeutic’s manufacturing facility, the MSAT (Manufacturing Science and Technology ) area and in APC Biologics when required. The Bioprocessing operator will be part of a team of operations professionals across a number of unit operations throughout the process and is responsible for executing batch operations as per standard operating procedures in line with designated production schedules under limited supervision.
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 3 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 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.
Ideally 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 COB 29/8/2025
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.