Join Our Team

Job Description:

This hybrid role bridges hands-on technical engineering with robust documentation and process management. The ideal candidate will be responsible for:

• Assembling and calibrating mechanical systems.
• Conducting experiments to validate prototypes and designs in lab settings.
• Developing clear and detailed assembly and work instructions in English for production teams.
• Supporting the transition from R&D to production, troubleshooting production line issues, and implementing effective solutions.
• Coordinating and processing Engineering Change Requests (ECRs) from initiation to closure, ensuring timely reviews, approvals, and documentation updates.
• Managed risk management documentation and supported configuration audits to maintain
  compliance with internal policies and medical device regulations.
• Collaborating with multidisciplinary teams, including system engineering, software, mechanical, and production teams.

Responsibilities:

NPI & Mechanical Assembly:

• Hands-on assembly, calibration, and testing of multidisciplinary systems (mechanics, motors, pneumatics, electronics, sensors, and control systems).
• Performing design validation studies and troubleshooting production issues.
• Creating comprehensive assembly and troubleshooting guides.

ECR Coordination:

• Managing ECR workflows to ensure seamless integration of changes across engineering disciplines.
• Updating configuration management systems, risk files, and technical documentation.
• Participating in audits and maintaining compliance with ISO 13485, FDA, and other regulatory standards.

Collaboration & Communication:

• Acting as a liaison between R&D and production teams to ensure product quality and manufacturability.

Job Requirements:

Education:

• Bachelor’s degree in Mechanical Engineering, Mechatronics, Electronics, or a related field.
• A practical engineering diploma in a relevant discipline may be considered with sufficient experience.

Experience & Skills:

• Hands-on experience in mechanical assembly, system calibration, and production
  troubleshooting.
• Familiarity with multidisciplinary systems (mechanical, electronic, and software integration).
• Experience with New Product Introduction (NPI) processes.
  o Proven expertise in managing Engineering Change Requests (ECRs) and associated documentation.
• A strong understanding of medical device regulations and risk management practices is an advantage.

Soft Skills

• Excellent technical writing and organizational skills.
• Strong problem-solving abilities, especially in dynamic production environments.
• Collaborative and communicative mindset to work effectively across departments.

Advantages:

• Experience in the medical device industry.
• Familiarity with configuration management, quality assurance, or ISO 13485 standards.
• Hands-on experience with document control systems and JIRA or similar tools.

Position scope: Full-time
Location: Yokneam Ilit

Job Description:

The candidate must be highly professional, passionate about his / her work, and a team player. He/she has to combine technical excellence with attentiveness to requirements and the ability to deliver on time and quality. The perfect candidate would have:

• Development of automation machines and improvement/maintenance of existing automation machines.
• Take part in the phase of transferring the consumables production line abroad.

Job Requirements:

• Education: Bachelor’s degree in Mechanical Engineering
• Minimum of 5 years of experience in mechanical design and engineering – Must
• Proven experience in designing and developing machines incorporating motors, sensors, actuators, pneumatic pistons, and electrical control panels.
• Experience in leading system development, including coordination and interface with software engineers, control engineers, and algorithm specialists.
• Advanced proficiency in SolidWorks.
• Strong understanding of mechanical design principles, materials, and manufacturing
  processes.
• High-level hands-on engineering skills including prototyping, testing, and troubleshooting.
• Experience with plastic injection and an understanding of manufacturing constraints and
  capabilities in this area – Advantage.
• Experience with systems incorporating electro-optics and machine vision technologies.
• Background in the medical device regulations (e.g., ISO 13485, FDA) and design controls – Advantage.
• Familiarity with product lifecycle management (PLM) systems and product development processes within regulated environments.
• Excellent verbal and written communication skills for clear documentation and effective
  collaboration with cross-functional teams.
• Strong problem-solving skills with the ability to analyze complex engineering challenges and implement practical solutions.
• Demonstrated innovation in product development, creating new designs, or improving
  existing systems.
• Ability to handle multiple projects simultaneously, with experience in managing time,
  budgets, and resources effectively.
• High attention to detail and precision in designs, documentation, and testing procedures.
• Familiarity with safety standards and risk management procedures, including FMEA (Failure Modes and Effects Analysis) and DFMEA (Design FMEA).

Position scope: Full-time
Location: Yokneam Ilit

Job Description:

• Coordinating and processing ECRs from initiation to completion.
• Ensuring timely review and approval of change requests by relevant stakeholders.
• Updating and maintaining risk management files and other related documentation.
• Participating in configuration audits to verify compliance with policies and standards.
• Maintaining comprehensive documentation, configuration management systems, and updated JIRA tickets.
• Ensuring that documentation is well-organized, and consistently up to date.

Job Requirements:

• Associate’s or Bachelor’s degree in Engineering, Quality, or a related field (or equivalent experience).
• Strong technical understanding of changes initiated by the system engineering, software, and mechanical teams.
• Excellent communication and collaboration skills for interacting with cross-functional teams.
• Exceptional organizational skills: Ability to efficiently manage multiple ECRs and tasks simultaneously while ensuring accuracy and adherence to timelines.
• Detail-oriented approach to ensure accuracy and compliance with documentation standards and regulatory requirements.
• Experience in managing ECRs or working within an engineering or R&D environment, preferably in the medical device industry.
• Familiarity with configuration management or document control processes.
• Background in quality assurance or quality management systems (e.g., ISO 13485).
• Knowledge of risk management practices.
• Familiarity with medical device regulatory requirements (FDA, IVDR).

Position scope: Full-time
Location: Yokneam Ilit

Job Description:

• Supervise the manufacturing machines & processes, ensuring quality work is done in a safe & efficient manner.
• Improve and define machines’ work instructions.
• Develop & execute (hands-on) plans that improve production efficiency, reduce costs, and minimize required labor.
• Identify & diagnose issues in production machines and provide effective solutions and training.
• Solve problems and manage fault investigations in the consumables production line.
• Coordinate R&D, Engineering & Operations-related activities in the production line and manage change implementation through the ECO process.
• Oversee & execute machine maintenance & service plan.
• Prepare & maintain machine documentation & records.
• Establish safety procedures & protocols to ensure workers well being.
• Carry out training on work procedures and enforcement of work according to procedures on the production line.
• Management of in-line QC (destructive and not destructive) tests of products from the production line.
• Responsibility for production yield.

Job Requirements:

The candidate must be highly professional, passionate about his/her work, and a team player. He/she has to combine technical excellence with attentiveness to small details, and the ability to deliver on time and quality.

• Degree in Mechanical Engineering / Practical Mechanic Engineer or similar.
• Proven experience in machinery automation, pneumatics, mechanics, optics, robotics, and
  control systems.
• Proven experience in contractor management.
• Proven experience with IQ / OQ / PQ processes.
• Relevant experience in a mid-size medical manufacturing organization of at least 3 years.
• Superb analytical, problem-solving, and critical thinking skills.
• Ability to make decisions under pressure.
• Great attention to detail and organizational skills.
• Relevant experience in a mid-size medical manufacturing organization of at least 3 years.
• Experience in writing new work procedures and updating existing ones.
• Experience with CAD software – advantage
• Strong leadership abilities.
• Superb written and verbal communication skills.
• Proficiency in MS Office
• Experience in ISO, CE & FDA audits.
• High-level English (reading and writing).

Position scope: Full-time
Location: Yokneam Ilit

Job Description:

The position involves alternating shifts: morning shift from 7:00 to 16:00 and evening shift from 16:00 to 24:00.

Join us and become part of PixCell’s amazing team!

Job Description:

As a QA & regulation Specialist, you will play a crucial role in ensuring the quality and regulatory compliance of our cutting-edge in vitro diagnostic (IVD) analyzers. You’ll work closely with our multidisciplinary teams to maintain and improve our Quality Management System (QMS) while supporting our global operations.

• Maintain and continuously improve the company’s QMS in accordance with internal procedures, international standards, and regulations.
• Support external and internal quality audits, including supplier audits.
• Prepare and maintain Technical Files for various products, and submit them to relevant regulatory bodies.
• Manage documentation for different products, including DMR, DHF, TF, and DHR
• Execute ongoing quality improvement processes, including ECO processes, reviews, trainings, and effectiveness assessments.
• Perform Corrective and Preventive Action (CAPA) activities.
• Conduct non-conformity (NCR) investigations and root cause analyses.
• Lead problem-solving initiatives using quality tools and methodologies.
• Collaborate with multiple departments including production, R&D, and operations.

What We Offer

• Opportunity to work on innovative medical diagnostic technology with global impact.
• A collaborative and dynamic work environment in a growing company.
• Competitive salary and benefits package.

Job Requirements:

• Bachelor’s degree in Biomedical Engineering, Material Science, Medical Laboratory Science, or a related field.
• Minimum 3 years of experience in a similar QA role within the medical device industry.
• Strong understanding of QMS processes and regulatory requirements, including ISO 13485 and FDA regulations.
• Experience with internal audits and quality documentation.
• Excellent project management and communication skills.
• High proficiency in English, both written and spoken.

Position scope: Full-time
Location: Yokneam Ilit

Job Description:

• Perform bank reconciliations for collections and payments.
• Conduct credit card reconciliations for Israeli and US entities.
• Handle expense reports and employee reimbursements.
• Record vendor and intercompany invoices to Priority.
• Collaborate closely with the procurement team regarding purchase orders and goods
  receipt (GR).
• Control and supervise aging reports.
• Prepare invoices for payments.

Job Requirements:

• Bookkeeper certificate, type 2 or 3.
• Experience with Priority software – an advantage.
• Proficiency in Microsoft Office (Excel, Word, PowerPoint).
• Ability to work effectively in a team and under tight schedules.
• Proficiency in reading and writing emails in English.

Position scope: Full-time
Location: Yokneam Ilit