Merck-posted 1 day ago
Full-time • Mid Level
Hybrid • Durham, NC
5,001-10,000 employees

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. The Specialist, Manufacturing Automation, is a member of the Focus Factory Automation team responsible for the assigned process control systems in support of manufacturing operations at our Manufacturing Division Vaccine Manufacturing Facility located in Durham, NC. Additional Responsibilities Understands and supports all GMPs, safety, and environmental regulations | Periodically reviews automation documents, preventive maintenance, and SOPs to ensure compliance with GMP and safety. Develops and supports corrective actions associated with automation related deviations/investigations. Communicates periodically with immediate supervisor about status of area of responsibility. Evaluates automated and information technology systems and develops strategies to optimize and ensure quality and stability of automation systems through future expansion, replacement, or upgrade. Uses technical knowledge to assure the efficient operation of variety of automated processing and information technology systems. Leads in installing and placing new equipment into operations | Develops solutions for automation problems | Oversees investigations of automation anomalies to prevent recurrence. Participates in audits and training programs in the area of responsibility. On‐floor support of manufacturing activities Identify and implement process/equipment improvements and manufacturing efficiencies. Maintain Technical Documentation Will provide off shift support as needed, to support 24/7 production operations.

  • Understands and supports all GMPs, safety, and environmental regulations
  • Periodically reviews automation documents, preventive maintenance, and SOPs to ensure compliance with GMP and safety.
  • Develops and supports corrective actions associated with automation related deviations/investigations.
  • Communicates periodically with immediate supervisor about status of area of responsibility.
  • Evaluates automated and information technology systems and develops strategies to optimize and ensure quality and stability of automation systems through future expansion, replacement, or upgrade.
  • Uses technical knowledge to assure the efficient operation of variety of automated processing and information technology systems.
  • Leads in installing and placing new equipment into operations
  • Develops solutions for automation problems
  • Oversees investigations of automation anomalies to prevent recurrence.
  • Participates in audits and training programs in the area of responsibility.
  • On‐floor support of manufacturing activities
  • Identify and implement process/equipment improvements and manufacturing efficiencies.
  • Maintain Technical Documentation
  • Will provide off shift support as needed, to support 24/7 production operations.
  • Minimum 2 years in process automation or computer systems validation
  • Robust problem‐solving skills and a proactive approach to problem‐solving
  • Previous experience in a GMP manufacturing related role
  • Strong written and verbal communication skills in English
  • Demonstrated project management capability
  • Experience troubleshooting automated process systems
  • Bachelors degree in engineering, computer science, or related field
  • Experience in PLCs, SCADA, DCSs, and OEM.
  • medical
  • dental
  • vision healthcare and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays
  • vacation
  • compassionate and sick days
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service