Posted On | - | Few Days Ago |
---|---|---|
Availability | - | Fulltime |
Openings | - | 1 |
Category | - | QA Consultant |
Posted On - Few Days Ago
Availability - Fulltime
Openings - 1
Category - QA Consultant
Position Overview
In this role, you will be responsible for successfully leading quality assurance projects within the pharmaceutical and medical device sectors. Your expertise in cell therapy manufacturing, cloud-based data management systems, and medical device remediation will be crucial in ensuring regulatory compliance and quality standards are met. You will act as a mediator and communicator between technical teams and regulatory bodies, applying industry best practices to achieve optimal outcomes. Mentoring and coaching internal teams will be a key aspect of this role, as you guide them in risk-based approaches and regulatory compliance strategies.
Responsibilities
Cell Therapy Manufacturing Data Integrity Remediation Deviations:
Scientific Data Management System Implementation In The Cloud
Medical Device Remediation Project
Mentoring Internal Quality Engineers And POD Teams
Qualifications
Additional Requirements
Join our team to make a meaningful impact in the pharmaceutical and medical device sectors. Apply your expertise in quality assurance and regulatory compliance to drive successful projects and mentor internal teams. Showcasing your ability to mediate between technical teams and regulatory bodies, you will play a vital role in ensuring adherence to industry standards and best practices. Flexibility in working across different time zones and fluency in German will be valuable assets in this position. Apply now to take the next step in your career!
Employment Type: Contractor