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Grand River Aseptic Manufacturing, Inc Labeling, Packaging, and Inspection Technicians a in Grand Rapids, Michigan

DescriptionuJOB SUMMARY/uPerform qualified visual inspections, labeling and packaging of all products and devices manufactured under the guidelines of established procedures and cGMP regulations with the guidance of a lead, coordinator and/or finishing supervisor. The Technician's secondary responsibility is to support in all other routine tasks within the Finishing Operations. This position is ideal for new graduates looking to enter the pharmaceutical industry. 1st (6am -2:15pm) , 2nd (2:30pm - 10:00pm), and 3rd (10pm - 6:15am) shift positions available; competitive wages, benefits, Off-Shift premiums, and great company culture!bruESSENTIAL DUTIES/uulliInspect, label, and package finished product./liliFollow all finishing procedures and PDA guidelines./liliAssist in equipment preparation, inventory management, stocking, staging, and production area sanitization duties as needed./liliAccurately document data and complete batch records as needed./liliPerform cleaning and sanitization duties as instructed by the applicable procedure./liliPerform routine maintenance of finishing equipment./liliAssist in maintaining a warehouse that adheres to FDA regulations. This includes, but is not limited to: hand truck and fork lift operation, receipt and management of incoming materials, sanitization, labeling, shipping, and distribution./liliActively participate in Continuous Quality and Safety Improvements./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 ABILITIES/uulliExperience in pharmaceutical packaging of regulated products with a thorough understanding of cGMP, FDA guidelines and multinational regulatory standards required./liliAbility to pass a vision screening and Visual Inspection Qualification testing./liliAbility to read, interpret, and relate Standard Operating Procedures and Quality standards./liliMust be detail oriented./liliStrong verbal and written communication skills./liliKnowledgeable of GMP standards and the ability to follow CFR guidelines./liliComputer literate and familiar with Microsoft applications./liliExcellent time management skills./liliActively participate in Continuous Quality and Safety Improvements./liliCreative and open-minded who fosters an environment in which sharing of ideas is encouraged./liliAbility to work well in a cross-functional team environment./li/ulQualified candidates possess a High School Diploma or its equivalent. Associate's Degree and/or equivalent preferred.BR/GRAM supports Equal Opportunity Employment