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Grand River Aseptic Manufacturing, Inc Quality Assurance Technician in Grand Rapids, Michigan

DescriptionuJOB SUMMARY/uPerforms all Acceptable Quality Limit (AQL) inspections after the visual inspection and packaging processing steps. Perform periodic retention inspections and routine document reviews.bruESSENTIAL DUTIES AND RESPONSIBILITIES/uulliPerform the incoming component and Finishing Operation AQL inspections (visual inspection, product labeling and/or packaging)./liliPerform Monthly logbook reviews/liliPerform routine GMP document reviews (inventory cards, logbooks etc.)/liliUphold procedures and processes for AQL./liliCommunicate effectively with manufacturing to prioritize AQL inspections./liliSample finished product for retention and perform monthly retention inspection./liliKeep abreast to GRAM standards and trends with regards to visual inspection of components and finished product./liliProvide input into SQIRs, CAPAs, Customer Complaints, and Deviation Investigations from the visual inspection aspect./liliMay perform material release or similar duties./liliPerform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practice./liliOpen to a flexible and fluid work environment./liliSupport Agency, customer and vendor audits as needed./liliResponsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices./liliPerform all other tasks, projects, and duties as assigned./li/ulbrRequirementsuDESIRED SKILLS AND ABILITIES/uulliDetail-oriented./liliEnergetic, self-motivated, organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment./liliResults oriented and efficient./liliCreative and open-minded individual who fosters an environment in which sharing of ideas is encouraged./liliDemonstrates confidence in decision making ability./liliTakes accountability and ownership of the AQL process./liliAbility to work independently and participate in a cross-functional team environment./liliMust have basic computer skills in Microsoft Word, Excel and Outlook./liliKnowledge of QA principles and procedures in a pharma, biopharma, and/or biotech manufacturing environment/li/ulThis level of knowledge is normally acquired through completion of a HS Diploma/GED. Previous visual inspection or quality assurance experience is desirable.BR/GRAM supports Equal Opportunity Employment

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