Manufacturing Technician - 219390

Overview:Tasked with overseeing the production of biologics, conducting operations in production facilities to facilitate downstream manufacturing in accordance with current Good Manufacturing Practices (cGMPs).Responsibilities:Prepare instruments, conduct downstream purification processes, and perform clean room tasks adhering to cGMP standards under supervision.Execute procedures outlined in GMP documentation, including SOP/MBR, and promptly communicate with the internal team regarding floor activities, escalating issues to supervisors when necessary; Document deviations from SOP/MBR requirements.Participate in deviation investigations and the implementation of Corrective and Preventive Actions (CAPAs).Maintain cleanliness in the clean room as per cGMP requirements, including equipment surface cleaning, periodic cleaning, and changeover cleaning.Assist supply chain and Engineering teams with equipment validation, calibration, and maintenance.Utilize support systems such as LIMS as needed during GMP production.Perform job-specific tasks in compliance with Regulations, International Standards, and Policies.Promote and practice safe work habits, adhering to safety procedures and guidelines.Requirements:High School Diploma/GED or College DegreePrevious experience in the Pharmaceutical industry preferredPrior experience in bulk biologics cGMP manufacturing is advantageous.Experience working in a manufacturing environmentFamiliarity with TFF skids, centrifuges, chromatography columns and systems, and/or UF/DF systems preferred.Strong communication skills, teamwork abilities, and capacity to foster positive collaborations with internal stakeholders, vendors, and clients to achieve common goals effectively.Must demonstrate self-motivation, flexibility, organization, and attention to detail.

Created: 2025-02-22