MSI Express is a single-source contract manufacturing and packaging company, delivering innovative engineering solutions from our strategically located network of manufacturing facilities.ROLE PURPOSE/ POSITION SUMMARY:The Document Control Specialist is responsible for the receipt, organization, maintenance and retrieval of all quality documents and records within the facility. The Document Control Specialist will also provide leadership and assistance to the plant operations in the areas of SQF compliance.KEY ACCOUNTABILITIES/PRIMARY DUTIES & RESPONSIBILITIES:Create and maintain federal and locally regulated quality system documentation and programs i.e., HACCP, FDA, SOP's GMP, SQF and other related quality records and programs.Daily distribution of batch sheets, startup sheets per schedule. Works closely with materials.Prepare and participate in customer and government regulatory audits as required and consistent with Food Safety Programs.Maintain a current document master list and master files for all products, ingredients and SKU's.Develop and maintain a document review process to ensure prompt revision of documentation to support audits, audit program, and pre-requisite programs.Ensure all programs and documents are properly approved.Distribute revised documents to necessary locations and remove obsolete revision.Drive improvement in documentation and streamline processes using Standard Work and current documentation.Develop and maintain SQF documentation (manuals, SOP's, registers, food defense program) to ensure compliance and investigate and resolve food safety issues.Develop and maintain AIB documentation, food handlers' documentation and USDA documentation.Incorporate customer, FDA and industry governed regulations' requirements to MSI Express Inc. documentation.Maintains hold log and assists with Hold resolution.Identify new SOP, SSOP's and instruction requirement: Follow through draft, approval, training, verification and implementation stages. Perform audits to ensure effectiveness.Proactively work with multiple departments to develop required documentation for smooth transition from sample run to production runs.Maintain SQF code awareness, reported operational GMP & HACCP deficiencies and consumer comments.Provide training materials around all things FSQ. Conduct FSQ and related training as required.Ability to define problems, collect data, establish facts, and draw valid conclusionsQUALIFICATIONS/ CAPABILITY PROFILE:Minimum SkillsAbility to work required hours and overtime as needed- EssentialAbility to follow work procedures and safety rules- EssentialAbility to read, write, communicate, understand, and follow directions/instructions- EssentialAbility to stand, walk, bend, crouch, stoop, reach, stretch, step, climb and/or sit frequently or through the duration of the shift- EssentialHave appropriate eye, hand and foot coordination to properly use various equipment and/or tools- EssentialAbility to work with minimal supervision- EssentialMinimum ExperienceHACCP Certified, SQF Experience, QI, PCQI- EssentialBasic lab experience, manufacturing experience, proven ability to follow written directions - EssentialProficient in Microsoft Word and Excel - EssentialAbility to read, write, and communicate effectively- EssentialAbility to read and write effectively in Spanish- DesirableAbility to process quality documentation within a timely manner accurately- EssentialHigh School Diploma- EssentialApply today and join our rapidly growing team!Inc. 5000 #1,085 fastest growing company in the USA. (2023)Inc. 5000 #622 fastest growing company in the USA. (2022)Inc. 5000 #479 fastest growing company in the USA. (2021)Inc. 5000 #10 fastest growing company in the Midwest. (2022)Inc. 5000 #165 fastest growing company in the Midwest. (2021)
