QC/ARD Assistant – Maternity Leave Cover (6-Month Contract)
Location: Onsite in Cashel, Co. Tipperary
Type: Full-time, Fixed-Term (Maternity Cover)
Salary: Competitive
We’re hiring a QC/ARD Assistant to join the laboratory team on a 6-month maternity cover contract. This role is suited to candidates with at least 1 year of laboratory experience in a GMP or regulated environment who are confident with laboratory procedures, equipment handling, and documentation practices.
This is not an entry-level position and would not be suitable for recent graduates or those with limited practical experience.
Key Role Details
- Contract Type: 6-month maternity cover
- Location: Onsite in Cashel, Co. Tipperary
- Schedule: Full-time, Monday to Friday, 8:00am – 5:00pm
- Onsite Requirement: Fully onsite, 5 days per week
- Commute Requirement: You must live within a 40-minute commute of the site
- Salary: Competitive, aligned with experience and responsibilities
- Visa Requirement: Minimum Stamp 1G visa. The employer cannot sponsor visas
- You must have full right to work in Ireland
- You must have completed your studies and be available to work full-time
Key Responsibilities
Laboratory Operations
- Support day-to-day lab activities and ensure continuous workflow
- Maintain equipment readiness and ensure all materials are available
- Maintain cleanliness and compliance in the lab environment
Documentation & GMP Compliance
- Prepare and maintain SOPs, protocols, and reports
- Adhere to GDP and GMP standards
- Escalate deviations or issues to relevant leads
Equipment Maintenance Support
- Assist in scheduling and logging of calibration and maintenance
- Coordinate with service providers when required
- Maintain accurate records per SOP
Inventory & Reagent Management
- Order, receive, and monitor stock levels
- Ensure proper labelling, storage, and documentation
Sample Handling
- Receive, track, and prepare samples for testing and shipment
- Store and segregate samples as per SOP
EHS & Audit Readiness
- Comply with site safety procedures
- Support audit preparation and ensure documentation is up to date
Training & Development
- Maintain up-to-date training records
- Participate in cross-functional projects when required
Candidate Requirements
- Minimum 1 year of experience in a GMP or regulated lab environment
- Strong lab-based skillset and understanding of quality systems
- Science-related qualification (degree or diploma)
- Comfortable working independently and following SOPs
- Strong attention to detail, organisational, and documentation skills
What We Offer
- A structured role within a regulated pharmaceutical lab
- Opportunity to further develop your lab experience
- A collaborative and supportive team environment
- Full training on site-specific systems and procedures
