Quality Control Analyst

Independent Solutions; Dublin; On-site; EUR 36,000 - 48,000; Full time

Job summary

Independent Solutions is seeking a motivated QC Analyst to join our Quality Control team in a GMP-regulated pharmaceutical/biotech environment. The role supports laboratory operations, sample management, documentation, and compliance initiatives, performing routine QC testing in line with approved procedures.

This 11-month, onsite contract offers opportunities to gain hands-on experience in a fast-paced lab, contribute to investigations and audits, maintain accurate records, and collaborate with

Qualifications

• Minimum Level 5 qualification in science or related field.
• Preferred Level 6/7 qualification in biology, biotechnology, microbiology, or life sciences.
• Experience in a GMP-regulated laboratory environment is advantageous.

Responsibilities

• Perform QC laboratory activities in accordance with GMP requirements and procedures.
• Participate in daily QC meetings and communicate testing progress.
• Ensure compliance with quality systems, SOPs, GMP standards and regulations.
• Maintain accurate laboratory records and documentation.
• Support investigations, troubleshooting, and root cause analysis.
• Assist with audit and inspection readiness activities.
• Prepare laboratory materials, labels, reagents, and solutions.
• Carry out routine equipment checks and calibrations.
• Support sample receipt, management, storage, disposal, and expiry monitoring.
• Generate and archive laboratory documentation.
• Maintain 5S housekeeping and organised laboratory areas.
• Collaborate with cross-functional teams and drive continuous improvement.
• Work shift patterns to match operational needs.

Skills

Attention to detail

Communication skills

Teamwork

Problem-solving

GMP environment

Adaptability

Education

Level 5 qualification in science

Level 6/7 biology

Level 6/7 biotechnology

Level 6/7 microbiology

Level 6/7 life sciences

Job description

Contract Type: Initial 11-Month Contract (Strong Potential for Extension)

Working Model: Fully Onsite

Role Overview

We are seeking a motivated QC Analyst to join a Quality Control team within a GMP-regulated pharmaceutical/biotechnology environment. The successful candidate will support laboratory operations, sample management, documentation activities, compliance initiatives, and routine QC laboratory testing while ensuring adherence to quality standards and regulatory requirements.

This is an excellent opportunity for candidates looking to gain or further develop experience within a pharmaceutical or biotechnology laboratory environment.

Key Responsibilities

• Perform QC laboratory activities in accordance with GMP requirements and approved procedures.
• Participate in daily QC meetings and communicate testing progress effectively.
• Ensure compliance with quality systems, SOPs, GMP standards, and regulatory requirements.
• Maintain accurate laboratory records and documentation.
• Support laboratory investigations, troubleshooting, and root cause analysis activities.
• Assist with audit and inspection readiness activities.
• Prepare laboratory materials, labels, reagents, and solutions as required.
• Perform routine laboratory activities including equipment checks, pH meter calibrations, and balance calibrations.
• Support sample receipt, management, storage, disposal, and expiry monitoring activities.
• Generate, review, file, and archive laboratory documentation.
• Maintain laboratory housekeeping standards and support 5S initiatives.
• Ensure laboratory areas remain clean, organised, and inspection-ready.
• Collaborate effectively with cross-functional teams and support continuous improvement initiatives.
• Work shift patterns in line with operational and business requirements.

Education

Minimum:

• Level 5 qualification or equivalent, preferably in a science-related discipline.

Preferred:

• Level 6 or Level 7 qualification in: Any
• Biology
• Biotechnology
• Microbiology
• Life Sciences or related scientific discipline

Skills & Experience

• Strong attention to detail and organisational skills.
• Good verbal and written communication skills.
• Ability to work effectively both independently and within a team.
• Strong problem-solving and troubleshooting abilities.
• Ability to work in a fast-paced GMP-regulated environment.
• Flexible, proactive, and adaptable to changing priorities.
• Experience within a laboratory, pharmaceutical, biotechnology, food, environmental, or regulated manufacturing environment would be advantageous.