Production Engineer

Company Description

Liposphere Ltd. is an innovative biomedical start-up founded in 2019 as a spin-off from the Weizmann Institute of Science in Israel. The company specializes in the development of cutting-edge, water-based biocompatible nanomaterials designed to achieve ultralow friction in critical conditions within the human body. Backed by over a decade of academic research, Liposphere has pioneered its technology through the revolutionary Hydration Lubrication Mechanism. Liposphere's proprietary technology is globally protected by intellectual property rights.

Position Overview

Be part of the manufacturing team, producing commercial batches.

Hands-on operational activities, such as maintenance, warehouse organization, raw material ordering, and reporting and coordinating the handling of production deviations with QA.

Working in a clean room environment under the ISO 13485 standard.

Optimizing and improving the existing process.

This is a full-time, on-site Production Engineer role located in Givat Shmuel, Israel.

Key Responsibilities

Ø Execute manufacturing activities according to production plans, including non-routine runs.

Ø Manufacture validation, clinical, and commercial batch.

Ø Support ongoing improvement of existing manufacturing processes.

Ø Perform and support process validation activities.

Ø Maintain manufacturing documentation (SOPs, work instructions, batch records).

Ø Support deviation investigations and CAPA activities with QA.

Ø Monitor raw material and packaging inventory and initiate purchase requests.

Ø Support warehouse and documentation activities in accordance with ISO 13485.

Ø Work closely with R&D, Engineering, Quality, and Regulatory teams.

Requirements

Ø Bachelor’s degree in engineering (Chemical, Biotechnology, Materials, Industrial Engineering, or related field).

Ø  2-3 years of experience in a Production / Process / Manufacturing Engineering role

Ø Experience as a Process / Manufacturing Engineer in a medical device company – advantage.

Ø Experience in process validation, deviation management, and documentation.

Ø Experience working under ISO 13485 – advantage.

Ø Experience in manufacturing validation, clinical, or commercial batches – advantage.

Ø Independent, organized, hands-on, and able to manage multiple tasks.

Ø Strong motivation and ability to work in a multidisciplinary team.