QA Specialist - 24/7 Shift

Hyper Recruitment Solutions; Waterford; On-site; EUR 42,000 - 60,000; Full time

Job summary

Hyper Recruitment Solutions is seeking a Quality Assurance (QA) Specialist for a leading pharmaceutical company in the County Waterford area. You will ensure products are manufactured, stored, and packaged in accordance with cGMP.

This is an initial 12-month contract with likely extension, featuring a 24/7 shift pattern: two days (07:00-19:00), two nights (19:00-07:00), followed by four days off. Key duties include supporting QA, training GMP packages, preparing and reviewing procedures and

Qualifications

• Degree in science or related field with GMP knowledge.
• Experience in a GMP environment is required.
• Working knowledge of cGMP regulations.

Responsibilities

• Work as part of the QA team to ensure cGMP compliance.
• Support development and delivery of GMP training packages.
• Prepare and review procedures and batch documentation.
• Conduct audits of all departments according to the schedule.

Skills

GMP knowledge

Quality assurance

Auditing experience

Training development

Regulatory compliance

Education

Bachelor's degree in a scientific discipline

Job description

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.