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Duration: Contract till Sep 2026 with possibility to extend
• Execute test scripts (design, execution, simulation, wet testing).
• Own change requests and complete change request tasks to support project completion.
• Deviations / Root Cause Analysis (RCAs).
• Assist the Quality department with deviation investigations.
• Assist with completion of CAPA actions.
• Participates in quality risk assessments.
Documentation
• Review/revise automation and Manufacturing related SOP’s, Functional Specifications, and work instructions, equipment/process changes, error prevention activities, etc.
• Author and review test protocols.
• Perform other duties as assigned.
Key Requirements:
• Bachelor's degree in an engineering or related discipline.
• Related work experience in a GMP environment.
• Strong communication and leadership skills.
• Ability to secure relevant information and identify key issues and relationships from a base of information.
• Ability to evaluate engineering problems and be able to devise cause and effect relationships and propose solutions.
• Ability to fulfill on-call hours requirements.
• VBA coding or Interface experience is plus.
Please contact me if you are interested. Thank you.
Thank You,
Gurpreet Kaur
Aequor Technologies LLC
377 Hoes Lane, Suite 300
Piscataway, NJ 08854
(732) 993-7304
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