Manufacturing Associate – cGMP API Production job opportunity at Eurofins.

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Date2026-05-11T15:00:51.255Z bot
Eurofins Manufacturing Associate – cGMP API Production
Experience: General
Pattern: Full-time
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degreeGeneral
loacation Groton, Connecticut, United States
loacation Groton, Connec..........United States
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Job DescriptionPosition OverviewYou will be a key member of a multidisciplinary manufacturing team supporting the cGMP production of non‑commercial clinical API batches. This role is hands‑on and process‑driven, contributing directly to API development by executing batch operations, supporting equipment qualification, and ensuring compliance with cGMP and safety standards. Work is performed in a pilot‑scale manufacturing environment with close collaboration across Quality, Compliance, and technical teams.Standard operations involve chemical synthesis of APIs, including solid and liquid handling, distillation, extraction, crystallization, filtration, and drying.Key ResponsibilitiesManufacturing OperationsExecute Process Operating Instructions and batch records in a regulated cGMP (GxP) environment.Prepare, operate, monitor, sample, and clean complex pharmaceutical manufacturing equipment according to SOPs.Perform hands‑on chemical processing activities, including:Solid and liquid chargingAtmospheric and vacuum distillationLiquid‑liquid extractions and phase separationsCrystallization, filtration, milling, and dryingPerform routine manual material handling, including lifting and moving loads ≥50 lbs using proper safety techniques.Identify, troubleshoot, and resolve equipment and process issues.Documentation & ComplianceGenerate, review, and execute cGMP documentation such as:Batch recordsCleaning recordsIn‑process control sampling documentationSupport equipment commissioning and qualification activities.Participate in SOP periodic reviews.Report deviations, observations, or safety concerns that may impact product quality or process safety.Ensure proper handling, segregation, and disposal of manufacturing waste in compliance with environmental and safety requirements.Collaboration & Continuous ImprovementCommunicate effectively across cross‑functional teams including Quality, Compliance, Process Chemists, Analysts, and Supervisors.Actively participate in shift handovers and operational communications.Identify and implement continuous improvement opportunities.Prioritize personal workload and support less‑experienced colleagues in task planning and execution.Complete required training and participate in facility safety inspections.

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