Develop, implement and maintain PLC/HMI programs and electromechanical systems for production lines; integrate systems with MES; lead troubleshooting, feasibility studies, validations, and global efficiency/innovation projects; create specifications, documentation, and technical standards; support qualification of automated systems and procure components for project workpackages.

The Operator is responsible for overseeing the production process, controlling product quality, and maintaining workplace cleanliness and safety standards while participating actively in team tasks.

Zarządzanie systemami kontroli w produkcji, kalibracja i konserwacja kamer oraz czujników, instalacja nowych systemów, analiza problemów.

The Operator oversees the production process, controls product quality, maintains records, and ensures workplace cleanliness while following safety protocols.

Oversee and maintain control systems in production, calibrate cameras and sensors, conduct preventive maintenance, and analyze problems to implement solutions.

Ensure quality assurance and compliance for ophthalmic dropper bottles, conducting tests and collaborating with R&D and production.

Support process optimization and improvement for syringe, vial and cartridge production. Assist root-cause analysis, implement improvements, support equipment testing, qualification, validation, documentation, and continuous improvement under senior supervision.

The role involves managing logistics for imports and exports, ensuring compliance with regulations, maintaining communication with suppliers and customs, and accurate record-keeping.

As a Customer Quality Engineer, you'll lead quality tasks in medical devices, manage risk and validation strategies, and ensure quality standards while collaborating with teams and customers.

The SCM Manager oversees inventory management, production control, and supplier relations to ensure timely delivery and cost effectiveness, while maintaining safety and quality standards.

Serve as primary liaison between production and IT for MES; implement, configure, and support MES/ERP/RPA systems; analyze and optimize end-to-end manufacturing processes; perform live-system customizations and validations; lead local IT projects, training, and change management while ensuring regulatory compliance (GMP, ISO 13485, 21 CFR Part 11).

As a Quality Control Associate, you will ensure production quality by performing inspections, conducting measurements, supporting batch releases, and investigating deviations.

As a Product Lifecycle Lead, you will coordinate the manufacturing process, collaborate with teams, monitor performance, and report on key metrics to improve efficiency.

The EHS Engineer will ensure compliance with health and safety standards, develop safety programs, conduct safety tours, and coordinate emergency response teams.

Supervise production activities in cleanroom environments, ensuring compliance with GMP, managing teams, and maintaining production records.

Manage order processes and ensure timely execution, including customer communication, scheduling, and procurement of materials. Participate in audits and inventory management.