Process Validation Specialist
About the Role:
We are seeking a skilled Process Validation Specialist to join our team. In this role, you will be responsible for executing FAT/SAT/IOQ protocols, designing and reporting on validation studies, and ensuring compliance with regulatory requirements.
Key Responsibilities:
* Develop and execute validation protocols and reports in accordance with industry standards and regulations.
* Collaborate with cross-functional teams to design and implement validation studies for equipment, systems, and processes.
* Ensure that validation studies meet or exceed regulatory requirements and company standards.
* Provide technical guidance and interpretation of validation requirements and regulations.
* Maintain accurate and detailed records of validation activities and results.
Requirements and Qualifications:
To be successful in this role, you will need:
* Degree in Science (Chemistry, Microbiology, or Pharmacy) or Engineering Chemical/Mech/Elec).
* 3-5 years experience working in a Healthcare manufacturing environment, ideally in the pharmaceutical sector.
* Strong technical knowledge of pharmaceutical plants and processes.
* Experience with process validation regulations and guidelines.
* Excellent problem-solving and analytical skills.
Benefits:
This is an exciting opportunity to work with a talented team and contribute to the development of our processes and procedures.
Others:
Please note that this role requires a high level of attention to detail and ability to work independently in a fast-paced environment.