Quality Assurance Specialist

Hyper Recruitment Solutions Ltd; Waterford; Sur place; EUR 42 000 - 66 000; Plein temps

Résumé du poste

Hyper Recruitment Solutions Ltd is seeking a Quality Assurance (QA) Specialist for a leading pharmaceutical company in County Waterford. The role ensures products are manufactured, stored, and packed in line with cGMP.

The position is a 12-month contract with a 24/7 shift pattern: two days (07:00-19:00), two nights (19:00-07:00), followed by four days off. You will join the QA team to support GMP training, procedures, batch documentation, and audits.

Qualifications

• Relevant degree in a scientific discipline is required.
• Proven industry experience in a GMP environment is expected.
• Working knowledge of cGMP regulations is essential.

Responsabilités

• Ensure compliance with cGMP for manufacturing, storage and packaging.
• Support the development and delivery of GMP training packages.
• Assist in preparation and review of procedures and batch documentation.
• Conduct audits of all departments according to the agreed schedule.

Connaissances

GMP experience

cGMP knowledge

Pharmaceutical

Audits

Quality Systems

Continuous Improvement

Regulatory Compliance

Training packages

Quality Specialist

Formation

Bachelor's degree in science or related discipline

Description du poste

We are recruiting a Quality Assurance (QA) Specialist to join a leading Pharmaceutical company in the County Waterford area. As the Quality Assurance (QA) Specialist, you will play a crucial role in ensuring that products are manufactured, stored, and packaged in accordance with current Good Manufacturing Practices (cGMP).

This is an initial 12 month contract with likely extension. Please note this is on a 24/7 shift pattern - Two days (07:00-19:00), two nights (19:00-07:00), followed by four days off.

Key duties and responsibilities:

• As the Quality Assurance (QA) Specialist, you will work as part of the Quality Assurance team to ensure compliance with cGMP.
• As the Quality Assurance (QA) Specialist, you will support the development and delivery of GMP training packages.
• As the Quality Assurance (QA) Specialist, you will participate in the preparation and review of procedures and batch documentation.
• As the Quality Assurance (QA) Specialist, you will conduct audits of all departments according to the agreed schedule.

Role requirements:

• Relevant degree in a scientific or related discipline.
• Proven industry experience in a similar role within a GMP environment.
• A working knowledge and practical experience with cGMP regulations.

Key Words: Quality Assurance / GMP / cGMP / Pharmaceutical / Batch Documentation / Audits / Quality Systems / Continuous Improvement / Regulatory Compliance / Training Packages / Quality Specialist

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements.