Process Validation Specialist

We are looking for a "Process Validation Specialist" (only local candidates will be considered) with the requirements below: Key Responsibilities: Monitor production activities on-site and participate in process validation batches as part of new product projects. Follow production operations and conduct the necessary assessments to ensure product safety and quality. Prepare manufacturing and packaging protocols. Prepare process validation and cleaning validation protocols and reports. Prepare and/or revise the necessary documentation related to new product processes and Annual Product Review (APR) activities, when required. Coordinate communication and organization with relevant departments and companies as part of Product Transfer activities. Prepare, update, and monitor Quality Assurance SOPs and documentation related to Product Transfer. Additional requirements: Bachelor’s degree in Сhemistry, Chemical Engineering, or Biology from a recognized university. At least 2 years of experience in Quality Assurance within the pharmaceutical industry. Advanced level of English proficiency. Thorough knowledge of current Good Manufacturing Practices (GMP). Good knowledge of manufacturing and quality control processes. Experience in process validation and domestic and international regulatory submission and product registration processes. Strong teamwork and interpersonal skills. Knowledge of project tracking and strong analytical thinking skills. Advanced proficiency in current office software and computer applications You are kindly asked to send your CV to the e-mail address in the Apply for job button by indicating the position name in subject on the following mail address.