Manufacturing and Documentation Team Leader – Medical Devices (Aesthetic Injectables)

Location: Lod

Company: Glyance Ltd.

Team size: ~10 employees

Glyance is a small and growing medical aesthetics company developing and manufacturing high-quality dermal fillers. We operate strictly under ISO 13485 and are preparing for CE certification. As a lean organization, we are looking for a hands-on Manufacturing and Documentation Team Leader who is comfortable working in a small team and taking real ownership of production activities.

This is a hands-on, mid-level role (2–5 years experience) focused on execution and documentation, not a senior management position. This role is well suited for a professional looking to grow hands-on experience in medical device manufacturing and quality documentation.

Position Overview

The Manufacturing and Documentation Team Leader will report directly to the Site Manager and will be responsible for the day-to-day management of production activities. This is a early-seniority role (2–5 years of experience), suited for someone who combines operational execution with strong quality awareness and documentation skills. Writing and maintaining SOPs, production protocols, and validation documentation is a central part of the role.

Key Responsibilities

• Authoring, updating, and maintaining SOPs, production protocols, batch records, and work instructions
• Writing and executing process validation, equipment qualification, and cleaning validation documents
• Hands-on management of daily manufacturing operations
• Supervision and coordination of production employees in a small-team environment
• Planning of inventory levels for raw materials, consumables, and finished products, including traceability
• Active involvement in CE certification preparation, audits, and inspections
• Close collaboration with Quality, Regulatory, and R&D functions
• Continuous improvement of production processes, documentation, and workflows

Required Qualifications & Experience

• Hands-on experience in writing production documentation and validation activities – absolute mandatory
• 2–5 years of experience in manufacturing, production, or quality roles within a regulated environment
• Medical device background – strong advantage
• Comfortable working in a small company (≈10 employees) with broad responsibilities and little hierarchy
• Strong attention to detail, structured work style, and high accountability
• Good written and spoken English

What We Offer

• A central role in a growing company
• Direct impact on production and shaping the company towards CE certification and regulatory readiness
• A hands-on position in a small, focused, and professional team
• High ownership and visibility across the organization

To apply, please fill out the online questionnaire here: https://forms.office.com/Pages/ResponsePage.aspx?id=6VG8W96lKEKoLfZZhJ_5RWUey42IarhAtn_UM1mmQANUMU00T0s5SEdSWUdOMUc2OEkwOUxRUkNUMS4u