Automation Engineering

Samsung Biologics

$120K — $160K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering or related field required
  • 5+ years of experience in automation engineering
  • Strong knowledge of cGMP and regulatory requirements
  • Familiarity with compliance standards such as SOPs, OSHA, NFP, BOCA/IBC
  • Experience with validation protocols (IQ, OQ, PQ) is a plus
  • Ability to communicate technical information effectively
  • Proficient in troubleshooting and optimizing manufacturing equipment

Responsibilities

  • Support interactions with various groups to troubleshoot and optimize systems
  • Provide engineering support for project execution to meet requirements
  • Ensure project compliance with cGMP and engineering practices
  • Document cGMP equipment modifications through change control
  • Generate validation protocols and provide technical support
  • Communicate project status and performance issues to management
  • Offer 24/7 emergency support for manufacturing operations

Benefits

  • 13 paid holidays
  • Vacation time
  • 401K match
  • Medical, dental and vision benefits effective day one of employment
Full Job Description
Samsung Biologics is seeking anAutomation Engineer to support process control systems, manufacturing equipment, building systems, and plant utilities at the Rockville, MD facility. This role is responsible for providing automation and control system engineering support for manufacturing operations, facilities, validation activities, and capital projects while ensuring compliance with cGMP and regulatory requirements.

KEY RESPONSIBILITIES:
  • Support/Interact with manufacturing/facility/lab/validation/quality groups to troubleshoot, optimize, test, and/or challenge equipment/systems
  • Provide engineering support for work requests for assigned area and project execution to ensure requirements are met, timelines are met, customer needs are addressed and projects align with GSK goals
  • Ensure all projects are compliant (cGMP, SOPs, OSHA, NFP, BOCA/IBC, Local and National Codes, etc.) and are executed with good engineering practice
  • Ensure a high level of compliance with cGMP and other regulatory requirements such as validation
  • Maintain and document all cGMP equipment/system modifications and upgrades through approved change control methods
  • Provide technical content and support for the generation of validation protocols; such as, Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ)
  • Communicate concerns and issues of staff, project status, performance and suggestions for improvement to management
  • Provide 24/7 emergency support to ongoing manufacturing operations


Education: Bachelor's Degree

The anticipated salary range for this position in Maryland is $120,000 to $160,000 plus annual bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc.

Benefits:
• 13 paid holidays
• Vacation time
• 401K match
• Medical, dental and vision benefits effective day one of employment

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