MES Author (Manufacturing Execution Systems) at Kelly Science, Engineering, Technology & Telecom in parsippany, New Jersey

Posted in Other 4 days ago.

Type: full-time





Job Description:

Kelly® Engineering is seeking a MES Author (Manufacturing Execution System) for an excellent direct hire position with an innovative company that holds a Great Places to Work certification in Parsippany, NJ. This position offers a salary up to $140K based on experience, dynamic growth potential and a positive team environment. If you are passionate about shaping the world we live in and are ready to reengineer your future, trust the experts at hiring experts.

MES Author Responsibilities:
  • Optimizing batch manufacturing processes, ensuring compliance with regulatory standards, and enhancing data integrity.
  • Collaborate with cross-functional teams, including manufacturing, quality assurance, and regulatory affairs, to gather information and resolve discrepancies
  • Responsible for the design, implementation, and maintenance of the Electronic Batch Records (eBR).
  • Create, manage, and maintain electronic batch records, including recipe management, process steps, electronic signatures, and data capture
  • Plan and execute validation tests (IQ, OQ, PQ) for eBR systems to demonstrate their compliance with regulatory requirements.
  • Oversee -User -Acceptance Testing of MES recipes to ensure business requirements are achieved
  • Ensure that all batch records and related documentation adhere to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
  • Initiate and process change controls related to batch records, ensuring that any deviations, revisions, or updates are properly documented and approved.

MES Specialist Requirements:
  • Bachelor's Degree in Engineering, Science or IT
  • Previous experience in Pharmaceutical manufacturing
  • Proficiency in MES eBR software platform Rockwell Automation PharmaSuite required
  • Strong understanding of regulatory requirements with batch processes, including FDA regulations (e.g., 21 CFR Part 11).
  • Familiarity with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) to ensure compliance.

What happens next:

Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in the Kelly Engineering network. That means our team of expert engineering recruiters will have access to your profile, making your opportunities limitless.
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