Experience Inc. Jobs

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA

Responsibilities:

• Under general supervision will evaluate, select and apply standard engineering techniques and procedures.

• Function as a technical expert to equipment or systems regarding troubleshooting operations. 

• Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of significant complexity.

• Work with Research, Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance and/or Validation departments in developing requirements and recommendations for system modifications.

• Work under the direct supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints.

• Work with consultants, architects and engineering firms on development of standard design documents.

• Develop process control applications utilizing Programmable Logic Controllers (PLC), Distributed Control Systems, Human Machine Interfaces (HMI) and Supervisory Control and Data Acquisition systems (SCADA).

• Familiarity with industry standards for batch control systems, software development life cycle methodologies, 21 CFR Part 11, and GAMP.

• Develop specification, engineering documents, SOP and operating standards.

• Troubleshoot and resolve equipment, automation or process issues in the field.

• Operate specialized laboratory equipment and computers as appropriate.

• Support non-standard shift organization including first, second, night, 12 hours and/or weekends shifts (24/7 operation)

• Provide solutions to a variety of technical problems of moderate scope and complexity.

Qualifications:

• Bachelor’s degree in Engineering (Mechanical, Electrical, Process Control and/or Chemical)

• 2 years of Engineering and/or Automation experience

• Background in programming, design, installation and lifecycle management of manufacturing process controls, automation and field instrumentation technologies.

• Working knowledge of pharmaceutical/biotech processes.

• Familiarity with validation processes and documentation in a highly regulated environment.

• Ability to read and update electrical design packages including User Requirements (URS),

• Functional Specifications (FS), Design Specifications (DS), wiring diagrams, and P&ID.

• Proficient in PLC Controller and HMI programming skills.

• Batch Process Control and recipe management.

• Distributed I/O configuration and troubleshooting.

• Industrial communication protocols Ethernet/IP, DeviceNet, and ControlNet.

• Rockwell Automation Factory Talk & ControlLogix PLC Platform.

• Rockwell Automation FTView SE and FTBatch systems.

• Rockwell Automation PanelView Plus.

• Data Historian - OSI PI Historian System and PI ProcessBook.

• Siemens TIA Portal HMI and S7 Controllers.

• Availability for 12hrs shift: Night shift

  Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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