Quality Assurance Regulatory Affairs Manager

You will manage a team of QA personnel responsible for QA Operation activities including but not limited to:

Responsibility for planning activities to support manufacturing of quality products ( QC, batch release, non-conformances, etc.)

Responsibility for supplier quality activities (qualification, audits, etc.)

Review and approve documents related to operations/ production as quality representative

You will Lead daily operational initiatives a proven track record of operational execution while retaining high quality of the deliverables.

You will analyse and present quality monitors

You will lead additional activities in the QA department upon needed.

Direct Manager: VP QA

Requirements:

BSc in Bio Medical / Bio- Technology or any other engineering, or CQE certification a must

Location - Netanya

Job skills:

3-6 years of experience in the medical devices industry, out of which at least 2 years in management position a must

Knowledge and experience in medical devices QA processes a must

Knowledge and experience in manufacturing in clean rooms a must

Experience in statistical analysis - advantage

Must be able to mentor Quality personnel in the necessary skills to review and approve highly technical documentation.

Computer skills: Proficiency in Office products - Must

Language skills: Fluent English - Mother tongue level

Personality:

Highly organized and detail oriented

Excellent interpersonal relations

Highly motivated and able to work independently in fast paced environment.

This position is open to all candidates.