The life sciences industry is quickly growing, bringing a huge demand for validation engineers. They are responsible for ensuring the safety and quality of pharmaceutical products and equipment. If you want to pursue your career in this field and wonder what validation engineer jobs are available and what skills you need, keep on reading!
Validation Engineer Jobs within the Life Sciences Industry
The following are the validation engineer jobs that you can explore in the life sciences sector to kickstart your professional career:
Equipment Validation Engineer:
Equipment validation engineers manage the manufacturing equipment and ensure it functions safely and reliably. They validate the GMP equipment and systems as per user requirements.
Developing and executing validation protocols, as well as maintaining compliance with global regulatory standards, is their responsibility. But that's not all; equipment validation engineers also have to conduct risk assessments and pinpoint potential validation issues.
If there are problems, they have to promptly troubleshoot and resolve them. For instance, they might notice that the steriliser is malfunctioning and contact the right vendor and repair personnel to fix it.
Computer Systems Validation Engineer:
A Computer Systems Validation ( also known as CSV) Engineer plays a key role in ensuring that computer systems used in regulated sectors—such as pharmaceuticals and medical devices—meet strict compliance standards.
Their work involves planning, executing, and documenting validation activities to confirm that systems operate reliably, consistently, and as intended, in line with regulatory expectations.
Cleaning Validation Engineer:
Cleaning validation engineers take care of all the cleaning procedures regarding the equipment used in manufacturing, particularly in pharmaceuticals and other biosynthetic products.
They design, plan, and execute cleaning activities within a facility. They provide technical leadership for deviation investigation relevant to cleaning activities (residual product/microbial contamination).
Moreover, cleaning validation engineers separate autoclavable (5,000-litre fermenter) and “Clean In Place” equipment (over 5,000-litre fermenter). Finally, these professionals have to write a cleaning report including, calculations and deviations as requested.
