Job Description
This is a challenging role for a highly motivated individual who wishes to make a significant contribution to the quality of our products.
We are seeking an experienced Quality Assurance Specialist to join our team. The successful candidate will be responsible for establishing and maintaining our operational and quality systems, ensuring continuous improvement through data monitoring and key performance indicator analysis.
The ideal candidate will have a strong background in pharmaceutical production, particularly in aseptic and terminally sterilized processes. They should possess excellent knowledge of EU GMP Annex 1 requirements and contamination control strategies in sterile manufacturing.
In this role, you will work closely with the Quality Assurance Manager to develop and implement strategies for equipment qualification, validation, and change control. You will also be responsible for conducting internal audits, managing regulatory inspections, and participating in supplier qualification.
Key Responsibilities:
* Establish and maintain operational and quality systems.
* Monitor data and key performance indicators to ensure continuous improvement.
* Develop and implement strategies for equipment qualification and validation.
* Conduct internal audits and manage regulatory inspections.
* Participate in supplier qualification and periodic requalification.
You will be working in a dynamic environment where no two days are the same. We offer a supportive team atmosphere and opportunities for growth and development.
If you are a driven professional with a passion for quality assurance, we encourage you to apply for this exciting opportunity.