GE HealthCare QC Validation Specialist 

Ireland, Cork 

184353321

As the QC Validation Specialist, you'll proved technical support to the QC Department and ensure QC systems, instrumentation, and processes are complaint, effective and implemented
Responsibilities

• Act as a technical and compliance liaison between QC functional teams and Operations/Engineering/QA.

• Provide technical support on QC instrumentation and product testing issue within the QC unit.

• Respond actively and troubleshoot test/instrument performance issues as notified by Operations/Engineering/QA.

• Technical expert in a wide range of chemical and microbiological equipment.

• Familiar with 21 CFR part 11 and how it applies to laboratory instrumentation.

• Sourcing, purchase and qualification of laboratory equipment.

• Carry method validation activities, through writing and executing protocol.

• Research new technologies to improve laboratory compliance and efficiency.

• Ownership of quality systems actions (IR's,CAPA,CC) ensuring timely closure and performance trending.

Required Qualifications

• Degree in Chemistry/ Microbiology, or in a science subject.

• Basic pharmaceutical experience in a GMP regulated laboratory environment

• Experience/ knowledge dealing with HPLC/ICP instrumentation is desired

Desired Characteristics

• Highly attentive to detail

• Self motivated, goal driven

• Experience in technical problem solving

• Good organisational skills

Total Rewards

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.