Validate and Comply:
As a senior validation specialist, contribute to critical validation activities that drive compliance and efficiency in the biopharmaceutical industry.
Key Responsibilities:
* Execute qualification and validation plans for life cycle management, adhering to cGMP and company procedures.
* Perform duties in accordance with GMP requirements, SOPs, and controlled documents, ensuring seamless operations.
* Model excellence in validation practices and promote adherence to corporate core values within the organization.
Essential Requirements:
* Bachelor's degree in an engineering or science discipline.
* Minimum 3-5 years' experience in pharmaceutical or similar GMP environments.
* Proven expertise in commissioning, qualification/validation of facilities, utilities, equipment, and instruments.
* Ability to troubleshoot and provide technical solutions for GMP manufacturing operations and equipment.