Quality Notifications and Investigations Specialist
Leverage your expertise in quality notifications and investigations to drive compliance and excellence in a leading biotech company.
Key Responsibilities:
* Author high-quality notifications, ensuring clarity, accuracy, and regulatory compliance.
* Develop and maintain quality-related metrics, facilitating effective communication and follow-up.
* Manage incident reporting, documenting quality issues and ensuring timely submission for review.
* Lead comprehensive investigation reports, detailing findings, root cause analyses, and corrective actions.
* Navigate approval processes for authored documents, collaborating with cross-functional teams.
Requirements:
* Bachelor's degree in Biotechnology, Chemistry, Biology, Pharmacy, or Process engineering.
* At least 2 years of experience in the biotech industry (bulk manufacturing of pharmaceutical or biological components).
* Strong technical writing capabilities and previous experience authoring reports and investigations in a GMP environment.
What We Offer:
Competitive contract opportunity with potential for growth and development.
How to Apply:
Apply via this advert or contact us if you have any questions about this opportunity. Skills: Deviations Investigations CAPA Technical Writing