Team Horizon Pharma Jobs – QA Specialist, Process Scientist, Micro Analyst, Qualified Person, and Validation Engineer Careers in Ireland
Explore top Team Horizon Pharma Jobs 2025 in Ireland – QA Specialist, Process Scientist, Micro Analyst, Qualified Person (QP), and Validation Engineer roles. Apply now for high-paying pharma careers in Dublin, Sligo, Mayo, and Roscommon. Work with leading teams ensuring global GMP, validation, and quality compliance.
Team Horizon Pharma Jobs – QA, QC, Validation, and Process Science Careers Across Ireland
Ireland continues to lead Europe’s pharmaceutical and biotechnological innovation, offering lucrative and stable career opportunities. Team Horizon, one of Ireland’s most reputable pharma recruitment and consulting companies, is hiring skilled professionals for various scientific and engineering roles in 2025.
🧪 1. QA Specialist – Team Horizon (Co. Sligo, Ireland)
Contract: 12-month fixed-term
Sector: Pharmaceutical Manufacturing
Location: Co. Sligo
Role Overview
The QA Specialist serves as a technical and compliance expert, overseeing quality assurance (QA) activities related to GMP and regulatory standards. You will act as the QA point of contact, providing technical guidance for new product introductions and manufacturing operations.
Key Responsibilities
- Review, approve, and maintain GMP documentation.
- Validate new product introduction documentation, protocols, and reports.
- Lead QA initiatives for cross-functional teams (Operations, QC, Engineering).
- Ensure timely document control and quality risk management.
- Support inspection readiness and continuous improvement projects.
Required Qualifications
- Bachelor’s degree in Science or Engineering.
- Minimum 5 years’ experience in a GMP Quality environment.
- Proven experience in validation and compliance.
- Excellent communication and document review skills.
Why Apply
Join a high-performance QA team contributing to globally recognized pharmaceutical excellence in Sligo. The QA Specialist position provides valuable exposure to EU and FDA compliance standards and long-term career growth.
⚗️ 2. Process Scientist / Engineer – Single Use Systems (Co. Sligo, Ireland)
Department: Technical Operations
Type: Full-time
Overview
Team Horizon’s Process Scientist role focuses on biologics manufacturing — optimizing single-use materials for sterile production. This position is ideal for professionals passionate about scientific innovation and process improvement.
What You’ll Do
- Develop and manage risk assessments for single-use material integration.
- Partner with vendors to implement best practices and validate SU assemblies.
- Lead experiments for new product manufacturing processes.
- Analyze process data and implement continuous improvement strategies.
- Collaborate with global science and quality teams.
Skills and Education
- Degree in Science, Biotechnology, or Engineering.
- 2+ years’ experience in biologics GMP environments.
- Experience with process validation and risk assessment.
- Familiarity with single-use technologies and E&L studies.
Why Choose This Role
This position offers deep involvement in bioprocess innovation and access to advanced manufacturing technology — critical for career advancement in biologics.
🧫 3. QC Micro Analyst – Dublin
Position Type: Full-time
Division: Microbiology Laboratory
Overview
The QC Micro Analyst ensures microbial quality testing of drug products, utilities, and materials — an essential role in ensuring patient safety and GMP compliance.
Key Tasks
- Perform sterility, endotoxin, and bioburden testing.
- Conduct water and in-process sample analysis.
- Prepare media and manage laboratory autoclaves and biological indicators.
- Write and review technical reports and validation documents.
- Participate in audits and implement continuous lab improvements.
Requirements
- Bachelor’s in Science or Microbiology.
- Experience in GMP QC microbiology testing.
- Knowledge of regulatory and cGMP standards.
Why Apply
Gain experience in one of Dublin’s most advanced pharmaceutical labs. You’ll develop specialized analytical skills while ensuring the microbiological integrity of world-class therapeutics.
🔬 4. Senior Associate – Quality Control (QC), Dublin
Sector: Laboratory Equipment Validation
Type: Full-time
Job Highlights
The Senior QC Associate manages the qualification, calibration, and maintenance of analytical laboratory instruments. This role ensures compliance with cGMP and FDA validation standards.
Responsibilities
- Oversee calibration and requalification programs using CMMS (Maximo).
- Plan and execute equipment validation protocols.
- Maintain documentation for equipment life-cycle management.
- Manage vendor maintenance and coordinate repairs.
- Act as SME for data integrity and instrument validation.
Qualifications
- Degree in Science or Engineering.
- Strong understanding of laboratory validation.
- 3+ years’ experience in cGMP-regulated environments.
- Excellent technical writing and project coordination skills.
Benefits
This position offers a hybrid of hands-on technical and QA responsibilities, giving you exposure to validation, compliance, and regulatory audit readiness.
💊 5. Qualified Person (QP) – Co. Mayo
Position: Full-time, Permanent
Industry: Biopharmaceutical Manufacturing
About the Role
As a Qualified Person (QP), you’ll oversee GMP operations, batch certification, and regulatory compliance. You’ll work directly with the QA Director to ensure the highest product quality standards across sterile manufacturing units.
Core Responsibilities
- Certify and approve batch records, exception reports, and quality reviews.
- Oversee QA operations for GMP and regulatory readiness.
- Manage non-conformance investigations and CAPA activities.
- Represent the company during regulatory inspections.
- Provide leadership for QA, QC, and Compliance teams.
Required Profile
- Degree in Pharmaceutical Science or related field.
- Recognized EU QP qualification.
- Minimum 5 years of experience in pharmaceutical QA or manufacturing.
Why Apply
This role provides leadership experience in one of Ireland’s most advanced pharma facilities. It’s an ideal step for professionals seeking regulatory authority roles and global influence in product quality.
🧾 6. QA Specialist – Supplier & Vendor Oversight (Co. Roscommon)
Contract Type: Permanent
Summary
This QA role focuses on supplier and vendor management — ensuring third-party service providers meet GxP standards. You’ll lead audits, qualify suppliers, and monitor global compliance systems.
Primary Duties
- Oversee GxP supplier qualification and audits.
- Develop supplier risk classifications and performance monitoring.
- Review supplier quality agreements and CAPAs.
- Conduct internal training on supplier compliance.
- Maintain eQMS and supplier database systems.
Qualifications
- Bachelor’s or higher degree in Life Sciences or Biotechnology.
- 7–10 years QA experience in Pharma or Biologics.
- Strong background in GMP, GLP, GDP, or GCP.
- Expertise in quality systems, technical agreements, and risk-based auditing.
Key Benefit
A global-facing QA role with extensive international collaboration and travel — ideal for candidates looking to build careers in global supplier quality and compliance.
⚙️ 7. QA Validation Engineer – Co. Mayo
Type: Full-time
Department: Quality Engineering
Overview
The QA Validation Engineer leads validation programs for equipment, utilities, and processes, ensuring that all operations meet FDA, EU cGMP, and GAMP guidelines.
Responsibilities
- Develop and execute validation master plans.
- Coordinate validation for equipment, software, and processes.
- Perform change control and deviation management.
- Create and maintain GMP validation reports and investigations.
- Train and mentor new validation team members.
Skills Required
- Degree in Engineering or Science.
- 3+ years in validation or QA roles.
- Strong understanding of GAMP and cGMP standards.
- Excellent problem-solving and documentation skills.
Why Apply
Work in a fast-evolving environment where your validation expertise ensures operational excellence. This position offers both leadership opportunities and direct involvement in compliance projects.
🌍 Why Choose Team Horizon Careers in Ireland?
Team Horizon is a trusted partner for Ireland’s pharmaceutical and biopharmaceutical industries. With clients across Europe and North America, they provide experts for GMP compliance, validation, QC, R&D, and process optimization.
Here’s why professionals choose Team Horizon:
- Global exposure to EU/FDA-regulated projects.
- Dynamic roles across QA, QC, validation, and bioprocessing.
- Competitive compensation and training programs.
- Opportunities to work on new product introductions (NPI) and sterile manufacturing innovations.
- Access to professional development and cross-functional career growth.
🔍 How to Apply for Team Horizon Jobs
Interested candidates can apply directly via:
Address: Chambers House, Ellison Street, Castlebar, Mayo, F23 DE92
Mayo, Ireland: +353 (0)98 50600
Dublin, Ireland: +353 (0)1 482 6920
