Job Description

The Quality Inspector is primarily responsible for supporting activities on the production floor. This includes room release, line clearance, in-process batch record review or post-executed review to ensure proper good documentation practices are followed. Provide quality oversight to all production areas to ensure product quality and compliance to cGMPs. This person works closely with operations personnel ensuring cGMP concerns are identified and resolved appropriately. Must be available/flexible to work second or third shift and weekends. DUTIES AND RESPONSIBILITIES Required to be on the floor and present to provide quality oversight for all critical manufacturing and packaging processes. Perform QA release and line clearance inspections and AQL checks on product. Performs on the floor logbook and in-process batch record review Perform Label Control functions (testing, issuance and reconciliation). Assist in the application and removal of pallet tags, Hold tags, and equipment out of service tags. Conduct review of batch records. Accumulate and organize data for Annual Product Reviews or other projects, as assigned by management. Identify deviations and ensure investigations are initiated by the appropriate personnel. Clearly communicate complex issues to Management personnel. Support creation / revision of SOPs to reflect current practices. Assist with FDA and other regulatory inspections. Perform all activities in compliance with Alora Quality Systems, site environmental, health, and safety rules; and applicable FDA and international regulations. Maintain knowledge of current regulatory requirements pertaining to drug product manufacture and packaging (cGMPs). Perform document control functions as needed. Perform annual retain inspections Release product contact supplies Perform sampling of incoming raw materials and for raw material retest. Test incoming printed materials against established specifications. Perform additional duties and responsibilities as assigned. EXPERIENCE AND QUALIFICATIONS High School Diploma or equivalent or technical school certificate. Two years of experience in, or support of, pharmaceutical or biotech GMP manufacturing. Proficient knowledge of a GMP production facility, manufacturing processes, and/or inspection processes. Demonstrated understanding and application of cGMP, current industries practices and relevant guidance. Excellent written and verbal communication skills. Ability to multi-task effectively. Position requires the ability to work independently and effectively in all areas of communication, collaboration, and decision-making. Great attention to detail with ability to work on multiple projects. Ability to organize and adapt to organization priority changes and work effectively with minimal supervision / independently with a sense of urgency. Proficient in Microsoft Office (Word, Excel). Preferred Experience / Skills Quality Assurance experience

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