Quality Inspector

Join to apply for the Quality Inspector role at Rani Therapeutics
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Base pay range: $37.00/hr - $42.00/hr

• Position Title: Quality Inspector (II, III, or Senior)
• Department: Quality Assurance
• Reports to: Quality Engineering
• Purpose of the Job: This Quality Inspector position will report to Quality Engineering. Main responsibilities include performing incoming inspections of materials/parts/products and reviewing and approval of manufacturing batch records and inspection records. This position will require to perform disposition of materials/parts/products. As a Quality Inspector, you will also support Quality Engineering with other Quality Management System (QMS) activities, such as assisting with environmental monitoring and quality metrics.

• Interpret drawings and specification documents.
• Perform incoming inspection of materials/components/subassemblies/finished products following standard operating procedures and using standard inspection tools, including the Micro Vu and Keyence.
• Determine inspection sample size based on procedures, specifications, and standards.
• Help develop inspection methods, including automated inspection programs using the Micro Vu and Keyence.
• Review/approve executed batch records for manufacturing and inspection records in accordance to QMS procedures and Good Documentation Practices.
• Approve/perform final disposition of materials/components/subassemblies/finished products.
• Assign and apply expiration dating labels to materials/parts/products, as per specifications/quality procedures.
• Initiate Non-Conformance Material Reports (NCMRs) and deviations when discrepancies are observed during inspections and record review process. Report discrepancies and issues to QA Engineering and affected function(s).
• Maintain materials in Quarantine (pending disposition) and MRB (under NCMR and deviations) in order.
• Maintain accurate records as per Document Control procedures.
• Support training of IQC personnel.
• Assist with performing environmental monitoring of Controlled Environment Rooms (CERs), as needed.
• Support Quality in the collection of quality metrics data.
• Interact closely with different functions of the organization.

• 2-5 years of experience performing inspections and reviews/approvals of manufacturing batch records/inspection records
• Government Regulated Environment experience such as FDA and ISO 13485
• Must have adequate computer experience (knowledge of Microsoft Word, Excel)
• Experience working in a cGMP environment

• Attention to detail and organizational skills
• Good interpersonal and communication skills
• Ability to work as a part of a team and promote a team environment

Mid-Senior level

Full-time

Quality Assurance

Biotechnology