Looking for an exciting opportunity to utilize your expertise in the pharmaceutical industry? As a key member of the QA department, reporting directly to the QA Compliance/Qualified Person, you will be responsible for managing the execution of validation activities and contributing to the preparation and review of the Validation Master Plan.
The successful candidate will have a minimum of 4-5 years of experience in a pharmaceutical environment, with a Bachelor’s degree in Science or Engineering. Knowledge of Process and Cleaning Validation, as well as the ability to conduct internal and external audits, is essential. Strong computer skills with Word, Excel, and any other statistical programs are also required.
Responsibilities include managing the validation requirements of the company and third-party suppliers, preparing and reviewing validation protocols and reports, and coordinating validation activities with relevant departments. Additionally, you will be responsible for maintaining and implementing the cleaning validation strategy and ensuring compliance with regulatory authorities.
If you are looking for a challenging and rewarding opportunity to make a significant contribution to the pharmaceutical industry, we encourage you to apply for this position.