Job Opportunity:
* We are seeking a qualified professional to execute validation activities following a life cycle approach, ensuring compliance with cGMP and company procedures.
* The successful candidate will be responsible for the authoring, reviewing, executing, and approving testing protocols and reports.
* They will also participate in project delivery, vendor inquiries, and the troubleshooting and monitoring of process systems.
* This role requires strong knowledge of GMP requirements and SOPs, as well as the ability to work flexibly and take on additional tasks as requested.
Requirements:
* A minimum of 3-5 years of experience working in a pharmaceutical or similar GMP environment is required.
* Experience in commissioning and qualification/validation of facilities, utilities, equipment, and instruments is essential.
* Maintenance of the validated state, requalification/revalidation, and equipment vendor package ownership are key responsibilities.
* Strong system design coordination skills are also necessary.