Project Manager in Quality and Regulation JB-4143

A company specializing in Quality Assurance and Regulatory Affairs for Medical Devices is seeking a Project Manager to join its team.

The company is a leader in its field, serving international companies, serial entrepreneurs, and operating at the forefront of both professional practice and academic excellence.

The role is part of a multidisciplinary team providing comprehensive regulatory solutions, including quality assurance, regulatory compliance, certification, international product registration, clinical studies, and usability engineering.

The primary objective of the role is to create value for clients while managing projects at the highest professional standard in the fields of quality and regulatory affairs, ensuring the achievement of both professional and commercial objectives.

Requirements:

• Engineering degree – an advantage.

• At least 10 years of experience as a Quality and/or Regulatory Affairs Manager in a medical device manufacturing company – mandatory.

• ISO 13485 Lead Auditor certification – mandatory.

• Passion for the field and a strong desire to grow, excel, and continuously develop.

• Excellent verbal and written communication skills in both Hebrew and English.

• Strong customer service orientation, excellent interpersonal and communication skills, and the ability to work effectively with multiple stakeholders.

• Willingness to work in the Sharon region and travel to client offices as required.