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Quality Control Incoming InspectorDepartment: Quality This QC Incoming Inspector is responsible to perform general inspection procedures for incoming raw materials. The position follows documented SOP and cGMP requirements during the performance of duties and completes required documentation and reports accurately and within specified time frames. The position completes all assigned tasks per cGMP and USP requirements and in compliance with Anika’s Quality System. For all raw materials and packaging components; Issues lot numbers and applies status labeling to each carton or container, inspects/tests per ANSI/ASQ Z1.4 and material part specification (MPS); completes documentation of inspection/testing results; generates a notice of approval form when product/component is released, updates status labeling accordingly Maintains accurate status of components being tested and released in ERP system Reports the results of testing Responsible for completion review of specific batch record elements according to SOP Tracks product returns Updates status labeling on product returns and verifies quantities for destruction Performs other duties as required The position requires a Bachelors degree in the life sciences or a related technical discipline and 2 years experience in a bio/pharma manufacturing environment. Experience with GMP, FDA and ISO requirements is required, with previous experience working in clean room environments preferred. Computer experience is required, and the ability to design and maintain spreadsheets is required. |
How to Apply
Our definition of a qualified applicant is an individual who has submitted a resume for a specific open position and has illustrated they possess the basic qualifications and skills within the position description.
To apply, select the job description and follow the links or send us your resume via e-mail to resume@anikatherapeutics.com.
No third party resumes accepted.
