Quality Assurance Specialist

NES Fircroft; Breda; Hybrid; EUR 40,000 - 60,000; Full time

Job summary

A leading recruitment agency is seeking a QA Specialist Intern located in Breda, Netherlands. This 12-month hybrid position involves supporting validation processes for a multinational pharmaceutical company. The ideal candidate holds a Master's degree in Engineering or Pharmaceutical Sciences and has 4+ years of experience in a GMP environment, with strong analytical and communication skills. Join a dynamic team to ensure compliance and quality in a fast-paced industry.

Qualifications

• 4+ years of experience in a GMP environment.
• Relevant experience in Equipment and Automation Validation.
• Experience with quality risk management tools.

Responsibilities

• Conduct validation of equipment and systems.
• Review and approve validation documentation.
• Support maintenance and engineering activities.

Skills

GMP experience

Risk management tools (FMEA)

Statistical analysis

Analytical skills

Communication skills

Education

Master's degree in Engineering or Pharmaceutical Sciences

Job description

Research Consultant Intern for the Pharma & Biotech industries @ NES Fircroft

Opportunity for a QA Specialist

Location: Breda (NL)

Duration: 12 months (with possibility of extension)

Office Attendance: hybrid

NES Fircroft is seeking a QA Specialist to support and oversight for validation of equipment, automation, and information systems for a multinational pharmaceutical company located in Breda.

Your Responsibilities:

• Process, equipment, and IS validation
• Reviewing and approving validation documentation
• Maintenance and Engineering support
• Managing ABR's device responsibilities and ensuring alignment with GMP regulations
• Quality Risk Management (QRM)
• Reviewing quality risk assessment reports
• Reviewing and approving changes to equipment

What We're Looking For:

• Master's degree in Engineering, Pharmaceutical Sciences, Process Technology or equivalent
• 4+ years of professional experience in GMP environment
• Relevant experience in Equipment and Automation Validation
• Proven experience with risk management tools such as FMEA, etc.
• Experience with statistical tools to support e.g. sampling plans and hypothesis testing
• Logical and linear analytical skills to evaluate and interpret complex situations
• Good verbal, written, and interpersonal communication skills

If you think you are just the right candidate for this role, apply now!