Dev Quality Assurance Specialist
il y a 1 semaine
The Clinical Manufacturing Quality team at Jefferson Wells Manpower Group is seeking a highly skilled Dev Quality Assurance Specialist to join our team. This role will be responsible for ensuring the establishment, implementation, maintenance, and continuous improvement of an effective Quality Management System (QMS) linked to product development.
Your Key Responsibilities:
- Ensure the GMP oversight of different laboratories and production pilots, including packaging, and outsourcing.
- Drive continuous quality improvement processes to ensure the Quality Management System in support of product development and clinical supplies works effectively.
- Provide support for qualification and validation activities of the different laboratories and production pilots.
- Identify, mitigate, and resolve compliance and quality issues that may affect company development activities and products.
- Manage Quality Assurance Agreements for New and Ongoing Suppliers.
Your Profile:
- Project Management Skills (tools like MS Project).
- Technical Knowledge in engineering, particularly in pharmaceutical production (secondary packaging and medical devices).
- Strong Communication Skills, including experience leading meetings and coordinating between teams.
- Experience in IT and Automation (networking, IT security, data integrity).
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