Join Our Team

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:

Quality Control and Assurance

• Lead and execute QC processes on the medical device production line, with a focus on in-process monitoring and control
• Implement and oversee in-line quality control processes to inspect products during their journey through the production line
• Create and implement monitoring points throughout the production process
• Conduct methodical investigations into production obstacles, aligning with industry quality standards
• Perform and oversee audits of raw materials intake and final product inspections
• Calibrate all production facilities and maintain calibration schedules

Process Improvement and Documentation

• Lead and execute ongoing production improvement initiatives
• Identify inefficiencies or deviations in production workflows, using tools like scatter charts or fishbone diagrams
• Write detailed internal reports on quality metrics, trends, and corrective actions
• Develop and update work procedures for various production stages
• Standardize and centralize quality data from production processes

Subcontractor Quality Management

• Conduct audits of critical subcontractors to verify compliance with ISO 13485 and other regulatory requirements
• Perform thorough inspections of raw materials and subassemblies at subcontractor sites
• Apply risk-based approaches to assess subcontractor processes
• Work closely with subcontractors to address non-conformities and implement corrective actions

Team Leadership and Collaboration

• Directly manage and mentor the QC team, fostering a culture of excellence
• Work closely with multiple departments, including production, R&D, operations, and external subcontractors
• Conduct and participate in internal and external audits

Job Requirements:

• Minimum of 3 years’ hands-on experience in a similar QC role, preferably in the medical device industry
• Demonstrated understanding of audit processes and quality control methodologies
• Proven ability to lead teams and implement process improvements
• Strong problem-solving skills and attention to detail
• Excellent communication skills in English, both written and verbal
• Bachelor’s degree in Engineering, Quality Assurance, or a related field
• High level of motivation and drive to advance and improve processes
• Ability to work effectively in a fast-paced, dynamic environment
• Strong analytical skills with a data-driven approach to problem-solving
• Willingness to be hands-on and lead by example on the production floor and at
  subcontractor sites

Job Description:

• Prepare and manufacture reagents for diagnostic technologies, ensuring all necessary components are included for the analyzers
• Strictly adhere to written preparation procedures and manufacturing schedules
• Complete work orders in a timely manner to support the production of diagnostic products
• Prepare buffers, solutions, and raw materials for the manufacturing process
• Conduct analytical tests at various key stages of production to ensure reagent quality and performance
• Maintain and calibrate manufacturing equipment to ensure optimal performance and durability
• Adhere to quality control procedures to guarantee the reliability of reagents
• Maintain accurate records and clean production areas to comply with regulatory requirements, good manufacturing practices, and standard operating procedures
• Assist with in-process testing to ensure that batches meet product specifications
• Maintain needed stock levels of raw materials and issue purchase requests as needed
• Collaborate with the supply chain department to ensure adequate supply of reagents to the production line
• Monitor inventory levels and communicate with relevant departments to prevent stockouts or overstock situations
• Contribute to the improvement of work instructions in collaboration with relevant engineering departments

Job Requirements:

• Associate degree in chemistry, biology, or a related scientific field
• 0-2 years of experience in a manufacturing environment, preferably in medical devices or diagnostics
• Familiarity with GMP standards and ISO 13485 quality management systems
• Attention to detail and ability to follow precise protocols
• Strong analytical and problem-solving skills
• Proficiency in computer skills, including use of Microsoft Office package (Word, Excel, PowerPoint)

Preferred Skills

• High level of precision in work execution
• Strong commitment to quality and continuous improvement
• Self-learning orientation and ability to quickly adapt to new technologies and processes
• Familiarity with automated manufacturing processes

Position scope: Full-time
Location: Yokneam Ilit