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Process Engineer – API Manufacturing Remediation

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Job Description - Process Engineer – API Manufacturing Remediation


Process Engineer – API Manufacturing Remediation



Location: Greater Madison Area, WI 


Duration: Minimum 6-month on-site project assignment


Position Type: Full-time consulting assignment

Position Overview

Automated Systems, Inc. is seeking a Process Engineer for a minimum 6-month on-site consulting assignment with an API manufacturer in the Greater Madison Area, Wisconsin. This role will support remediation and manufacturing improvement efforts at a biologically derived API site producing enzymes. The site also supports broader recovery and purification capabilities used in natural-product and biopharmaceutical processing.

The selected engineer will work directly with manufacturing and quality teams on organ/raw-material receiving and initial processing, API-contact equipment condition, wet-cake handling and storage, drying operations, solvent-based extraction steps, precipitation, centrifugation, filtration, ultrafiltration, reverse osmosis, chromatography, and related remediation activities.

Key Responsibilities



  • Serve as a process and remediation engineer supporting API manufacturing operations, technical problem-solving, and quality-system improvement initiatives.

  • Partner with Manufacturing, Quality, Validation, Technical Services, Regulatory, and site leadership to investigate deviations, OOS results, complaints, and process failures, and help ensure appropriate technical follow-through.

  • Lead or support root-cause investigations using sound engineering and quality-risk-management principles; ensure investigations are data-driven, well-scoped, and extended appropriately to related lots, materials, processes, and systems where warranted.

  • Evaluate process equipment, materials of construction, contact surfaces, and maintenance practices to improve suitability for CGMP manufacturing and reduce contamination risk.

  • Support implementation of preventive maintenance, inspection, equipment monitoring, repair follow-up, and lifecycle improvements for manufacturing equipment and supporting infrastructure.

  • Plan and execute studies, trials, and technical evaluations in support of process improvements, CAPAs, validation activities, and manufacturing readiness.

  • Develop and revise technical documents such as protocols, reports, assessments, engineering justifications, operating procedures, scope documents, change controls, and remediation action plans.

  • Provide technical support for batch-impact assessments, retain-sample evaluations, and risk assessments associated with manufacturing events or equipment-related concerns.

  • Help strengthen contamination-control practices for animal-derived API operations, including practical controls for process variability, hold decisions, escalation, and disposition support.

  • Coordinate contractors, technicians, validation resources, and cross-functional contributors as needed to execute projects and remediation tasks.

  • Identify opportunities to improve methods, systems, and operating discipline, and help convert those improvements into standard practice.






Requirements



Qualifications



  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Industrial Engineering, or a related technical discipline.

  • Engineering experience in a pharmaceutical, biotech, API, medical device, food, or similarly regulated manufacturing environment.

  • Ability to analyze process, equipment, and quality data; identify key factors; and recommend practical corrective actions.

  • Interpersonal skills to negotiate priorities, reconcile differences, and maintain momentum in a cross-functional environment.

  • Ability to work independently, manage multiple assignments, and drive issues to closure without excessive direction.

  • Comfortable operating in a fast-paced project environment with shifting priorities and significant visibility.


 








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