Our organization is currently seeking a highly skilled Validation Specialist to join our team. This exciting opportunity is perfect for individuals with experience in the pharmaceutical industry, specifically in validation and compliance. In this role, you will be responsible for executing cleaning cycle development and performing equipment qualification.
The ideal candidate will possess a strong background in chemical engineering, biochemistry, microbiology, or chemistry, as well as relevant work experience in validation and quality assurance. You should have a proven track record of adhering to regulatory guidelines and ensuring compliance with site EHS policy, cGMP, and other business regulations.
Your responsibilities will include reviewing and approving documents, ensuring documentation complies with standards, and providing technical input and support to cross-functional project teams. Additionally, you will represent our organization on regulatory inspections and participate in risk assessments, audits, and incident investigations.
As a key member of our team, you will ensure the highest Quality, Compliance, and Safety standards are maintained by participating in our Manufacturing Division Quality Management System (QMS) requirements. If you are a motivated and detail-oriented individual with a passion for validation and compliance, we encourage you to apply for this exciting opportunity.