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.
