We are seeking a Quality Assurance Specialist to support our operations in Torres Vedras. The ideal candidate will be responsible for maintaining compliance with regulations and ensuring adherence to quality standards.
Key Responsibilities
1. SOP Development and Review: Create, review, and revise Standard Operating Procedures (SOPs) to guarantee compliance with regulatory requirements and Good Manufacturing Practices (cGMP).
2. Deviation Identification and Reporting: Identify, classify, and report deviations from expected outcomes, and collaborate with teams to resolve complex minor and major issues.
3. Remediation and CAPA Activities: Oversee remediation activities, including the development of Corrective Action Preventative Actions (CAPAs), to maintain production continuity and ensure timely closure of investigations.
4. Quality Oversight: Provide quality oversight to the change management system for cell-related changes, ensuring seamless implementation and minimal disruption.
The successful candidate will possess excellent communication skills, attention to detail, and experience in quality assurance or a related field. They will also be able to work independently and collaboratively as part of a team.
This is an exciting opportunity to contribute to our mission of improving human life and health, working on challenging projects, and developing your skills alongside a talented team.
To succeed in this role, you will need strong analytical skills, the ability to work under pressure, and a passion for delivering high-quality results. If you are motivated by a fast-paced environment and committed to excellence, we encourage you to apply for this challenging position.