Sr Engineer - Software
Planet Pharma - Thousand Oaks, California, United States, 91362
Work at Planet Pharma
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Overview
Sr Engineer - Software
role at
Planet Pharma .
**Job Responsibilities:**
Develop process control applications utilizing Programmable Logic Controllers (PLC), Distributed Control Systems (DCS), Human Machine Interfaces (HMI), and Supervisory Control and Data Acquisition systems (SCADA).
Support projects focused on improving process equipment, utilities, and facilities, including sophisticated unit operation skids for integrating new drug product manufacturing technologies into clinical and commercial facilities.
Familiarity with industry standards such as 21 CFR Part 11, GAMP, and software development life cycle methodologies.
Develop detailed specifications, engineering documents, SOPs, and manage computerized system administration. Test automation-based process equipment.
Own and administer process control automation in a GMP-regulated manufacturing setting, including managing process change control requests.
Lead root cause analysis, incident investigations, and troubleshooting of process control issues involving mechanical, electrical, instrumentation, and control systems.
Support new product and technology introductions through engineering assessments, automation system configuration changes, and engineering runs.
Innovate solutions to complex problems by adapting standard automation principles.
Maintain a safe working environment by adhering to environmental health and safety regulations.
**Minimum Qualifications:**
Doctorate OR Masters + 2 years related experience OR Bachelors + 4 years OR Associates + 8 years OR High school diploma/GED + 10 years.
**Preferred Qualifications:**
B.S. or M.S. in Electrical, Chemical, Mechanical, or Biotech Engineering.
Strong background in control system automation, specifically in design, installation, programming, and validation.
5+ years experience with Rockwell Automation Factory Talk & ControlLogix PLC.
Experience with electrical design packages, validation documentation, and control techniques like S88 and S95.
Leadership, communication, and technical writing skills.
Flexibility to support 24/7 operations, including on-site and after-hours work.
Experience with automation strategies for new product and technology deployment.
Knowledge of systems such as Lyophilizer, Filling, Building Management, and utilities like WFI, Clean Steam, and sterilization equipment.
Proficiency with building automation, electronic batch records, and industrial communication protocols.
Understanding of cGMP procedures, change control, nonconformance, and validation practices.
Self-motivated, organized, and collaborative team player.
The position is full-time, located in Chatsworth, CA, with a pay range of $63-$73/hr depending on experience. The job posting is active and not expired.
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