Overview
On Site
$50 - $54 hr
Contract - Independent
Contract - W2
Contract - 12+ mo(s)
Skills
AUTOMATION
CONTROL
PACKAGING
ELECTRICAL
PLC
ROCKWELL
ALLEN-BRADLEY
FACTORY TALK
CONTROLLOGIX
FACTORYTALK
CONTROL LOGIX
DESIGN
CHANGE
GMP
REGULATED
CFR
PHARMA
MANUFACTURING
Job Details
Payrate: $50.00 - $54.00/hr.
Summary:
The Engineer position reports to the Manager of Engineering under the Engineering & Maintenance team at the facility. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations in the manufacturing facility. The site of the new advanced product assembly and packaging plant, this role will apply advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, processes, and/or capital projects.
Responsibilities:
Basic Qualifications:
Preferred Qualifications:
Top 3 Must Have Skill Sets:
Pay Transparency: The typical base pay for this role across the U.S. is: $50.00 - $54.00/hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.
For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy ().
Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions. By applying for this position, you agree to Aditi s use of AI technology, including calls from an AI Voice Recruiter.
#AditiConsulting
#25-21096
Summary:
The Engineer position reports to the Manager of Engineering under the Engineering & Maintenance team at the facility. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations in the manufacturing facility. The site of the new advanced product assembly and packaging plant, this role will apply advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, processes, and/or capital projects.
Responsibilities:
- System Design and Development:
- Design and develop automation systems and control strategies for packaging machinery and processes.
- Implement and configure Programmable Logic Controllers (PLCs), Human-Machine Interfaces (HMIs), and other automation equipment.
- Create and maintain detailed documentation, including system specifications, design documents, and operational procedures.
- Integration and Optimization:
- Integrate new automation technologies and equipment into existing packaging systems.
- Optimize control processes to enhance efficiency, reduce waste, and improve product quality.
- Conduct feasibility studies and cost-benefit analyses for automation projects.
- Troubleshooting and Support:
- Diagnose and resolve issues with automation systems and control equipment.
- Provide technical support and troubleshooting for production and maintenance teams.
- Perform system upgrades and maintenance to ensure optimal performance and reliability.
- Compliance and Quality Assurance:
- Ensure that all automation systems comply with FDA regulations, GMP standards, and industry best practices.
- Collaborate with Quality Assurance and regulatory teams to address any compliance or quality issues related to automation.
- Project Management:
- Lead and manage automation projects, including planning, execution, and monitoring.
- Coordinate with cross-functional teams to ensure timely and successful project completion.
- Prepare and present project reports, performance metrics, and technical documentation.
- Training and Development:
- Train and support staff on the use and maintenance of automation systems.
- Develop training materials and conduct workshops to enhance team competency in automation technologies.
Basic Qualifications:
- Master s degree or bachelor s degree and 2 years of Automation experience in Pharmaceutical, Medical Devices, or Biotechnology industries Or associate s degree and 6 years of Automation experience in Pharmaceutical, Medical Devices, or Biotechnology industries Or High school diploma/GED and 8 years of Automation experience in Pharmaceutical, Medical Devices, or Biotechnology industries
Preferred Qualifications:
- Advanced degree in Mechatronics, Computer, Electrical, Mechanical, or Chemical Engineering
- Knowledge and/or experience of pharmaceutical/biotech processes, especially in the area of final drug product operations
- Knowledge in Data Integrity and Security
- Extensive understanding and background in programming, design, installation, validation, and lifecycle management of manufacturing process controls, automation, field instrumentation technologies
- Exposure to Machine Vision, Serialization, Robotics, Siemens, and Rockwell software platform
- Ability to interpret and apply GAMPs and GMPs and familiarity with documentation in a highly regulated environment
- Comprehensive understanding of validation protocol execution requirements as well as knowledge of validation processes and requirements as applied to new equipment installations
- Organizational, project management, problem-solving, as well as validation protocol, and technical writing capability
- Excellent communication (verbal/written) and presentation skills
- Demonstrated interpersonal skills, including collaboration, influencing, and facilitation
- Understanding of Operational Excellence and Lean Transformation in the Automation and Engineering Context
Top 3 Must Have Skill Sets:
- PLC/HMI Troubleshooting (Rockwell, B&R, Siemens)
- Industrial Packaging experience
- Electrical Design
Pay Transparency: The typical base pay for this role across the U.S. is: $50.00 - $54.00/hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.
For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy ().
Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions. By applying for this position, you agree to Aditi s use of AI technology, including calls from an AI Voice Recruiter.
#AditiConsulting
#25-21096
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.