* Lead and manage the technical aspects of automation systems for packaging and ancillary equipment, ensuring optimal functionality and performance.
* Analyze and develop strategies to optimize manufacturing processes, focusing on minimizing downtime and improving operational efficiency in a highly regulated environment.
* Lead cross-functional teams and projects, driving continuous improvement and automation initiatives across departments including Research, Manufacturing, Process Development, Quality Assurance, and Validation.
* Contribute to the design, specification, and implementation of system modifications, experiments, and capital projects. Ensure effective deployment of new or improved engineering techniques and procedures.
* Work with various departments to define and develop requirements for complex system modifications and facility improvements.
* Ensure that all engineering processes, changes, and updates adhere to applicable industry standards (e.g., GMP, GAMP), maintaining compliance with relevant documentation and validation protocols.
* Oversee the lifecycle of automation systems, including design, installation, validation, and ongoing performance monitoring.
REQUIRED QUALIFICATIONS:
* Master's degree in Engineering (preferred) OR
* Bachelor's degree in Engineering with at least 2 years of Automation experience in Pharmaceutical, Medical Devices, or Biotechnology industries OR
* Associate"s degree in Engineering with 6 years of relevant experience in the Pharmaceutical, Medical Devices, or Biotechnology industries
PREFERRED QUALIFICATIONS:
* Advanced degree in Mechatronics, Computer Engineering, Electrical Engineering, Mechanical Engineering, or Chemical Engineering
* Knowledge and experience with pharmaceutical/biotech processes, particularly in final drug product operations
* Familiarity with Data Integrity and Data Security in regulated environments
* In-depth experience with programming, design, installation, validation, and lifecycle management of manufacturing process controls and automation systems
* Experience with Machine Vision, Serialization, Robotics, Siemens, and Rockwell software platforms
* Strong understanding of GMP (Good Manufacturing Practices) and GAMP (Good Automated Manufacturing Practice), including associated documentation requirements in regulated industries
* Experience with validation protocols and knowledge of the processes and requirements for new equipment installations
* Strong project management skills with proven ability to handle complex tasks and drive improvements
* Excellent verbal and written communication, presentation, and technical writing skills
* Proven ability to collaborate with cross-functional teams and lead projects from conception to completion
* Familiarity with Operational Excellence and Lean Transformation principles, particularly in automation and engineering contexts
* Expertise in PLC and HMI programming with specific experience in Rockwell, B&R, and Siemens systems
If you are interested in this role, please apply via the apply now link provided. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed. Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We are the employer of choice for thousands worldwide. For more information, please visit our website at Belcan.com