Quality Assurance Specialist

Hyper Recruitment Solutions Ltd; Waterford; Presencial; EUR 42.000 - 58.000; Jornada completa

Descripción de la vacante

Hyper Recruitment Solutions Ltd in Waterford is seeking a Quality Assurance (QA) Specialist to ensure that products are manufactured, stored and packed in full compliance with cGMP.

This 12-month contract includes a 24/7 shift pattern (two days 07:00–19:00, two nights 19:00–07:00, followed by four days off) and offers an opportunity to contribute to continuous improvement in a leading pharmaceutical setting.

Formación

• Degree in a scientific or related discipline.
• Proven experience in a GMP environment.
• Practical knowledge of cGMP regulations.

Responsabilidades

• Ensure products are manufactured, stored and packaged per cGMP.
• Support GMP training packages.
• Prepare and review procedures and batch documentation.
• Conduct audits across departments per schedule.

Conocimientos

GMP experience

cGMP knowledge

Auditing & QA systems

Educación

Bachelor's degree in a scientific discipline

Descripción del empleo

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:

Your duties as the Quality Assurance Specialist will be varied; however, the key duties and responsibilities are as follows:

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

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the Quality Assurance Specialist, we are looking to identify the following on your profile and past history:

• 1. Relevant degree in a scientific or related discipline.
• 2. Proven industry experience in a similar role within a GMP environment.
• 3. 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. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.