QC Technician Jobs in Michigan

Job Title: Quality Control Technician Company: Location: Grand Rapids, MI Description: QC Technician - Food Manufacturing Industry A Grand Rapids food manufacturer is accepting applications for a full-time, QC Technician. A minimum of two years prior experience in the food industry is required. The successful candidate will understand and enforce adherence to quality, GMP and HACCP requirements as well as have a good understanding of issues relevant to the food industry (allergen control and food plant sanitation). Responsibilities ? Monitor in-process and finished product specifications. ? Initiate corrective action procedures and documentation. ? Perform GMP and HACCP related self-inspections. ? Data entry ? daily reports, lot tracking, product specifications. ? Perform routine checks and monitoring of metal detectors, metal detectable band-aids, magnet checks, stock rotation etc. ? Collect product for sensory, incoming raw material samples and retains per customer requirements. ? Initiate foreign material reports and investigate root cause. ? Audit and file daily production records . ? Improve and/or report unsafe, unsanitary or inappropriate conditions ? Assist in- training co-workers to implement procedures required to meet quality and food safety program goals. ? Accommodate flexible scheduling to cover extended or other shifts. ? Maintain professionalism at all times, ? Represent quality assurance in committees as needed. ? Perform laboratory testing for moisture analysis, color verification, free fatty acid testing and water activity levels. Working Conditions: Must be able to walk to and from production lines, the warehouses and offices and may need to stand for long periods of time. Position involves lifting, bending, reaching, grasping, writing, reading, operating a computer, keyboard and telephone. Education Requirements: ? Education: High school diploma or equivalent ? Experience: Minimum 2 years in a food manufacturing facility; food related college courses would be beneficial. ? Other: Person must have strong communication, telephone and writing skills. Basic math skills (addition, subtraction, multiplication, division, decimals and fractions). Basic computer knowledge of Microsoft Word, Excel and Office. Required Skills and Experience ? Must be energetic, self motivated, dependable, flexible, detailed, and organized. ? Experienced in sample collection and documentation. ? Sensory training preferred. ? Strong analytical and reporting skills. ? Knowledge of federal and state food industry regulations is a plus. ? Understanding of sanitation and pest control practices is a plus. ? Knowledge of HACCP, SPC, GMP?s, SQF and third party audits is preferred.

Job Title: Quality Control Specialist Company: Location: Battle Creek, MI Description: Seeking Quality Control Specialist to work for a plastics manufacturer for full-time trial-hire position on 1st shift. Must have experience working in quality control, previous experience with customer relations and familiar with all measurement tools. Must also be proficient on computers. Experience driving a forklift and valid driver's license a plus, will help in Shipping and Receiving area. Must also have a HS diploma/GED and provide proof when applying for position.

Job Title: Quality Control Associate Company: Todays Office Professionals Location: Troy, MI Description: Job Purpose:Assures quality product by conducting in-process inspections; evaluating finished product.Duties:* Determines quality and reliability standards of product.Conducting in-process inspections and physical tests on cellular phones. * Determines disposition of finished product by collecting, classifying, analyzing, and interpreting production and quality data; judging product acceptability in comparison to specifications.* Determines acceptability of rework by conducting inspections and physical tests of reworked product.* MUST HAVE HIGH ATTENTION TO DETAIL! EXPERIENCE WITH SMALL PARTS HIGHLY PREFERRED!!THIS IS NOT JUST ANOTHER JOB THIS IS A GREAT OPPORTUNITY!!  MUST HAVE 1 year of education after High School ( NO certificates or online classes) and must have High School diploma, NO GED's. Shifts will differ:  M-F 8:00am - 5:00-pmMUST HAVE OWN TRANSPORTATIONATTENDANCE IS CRUCIAL! CAN NOT BE LATE OR MISS WORK FOR FIRST 30 DAYS UNDER AND CIRCUMSTANCE OR YOU WILL BE DISMISSED!!

Job Title: Quality Control Technician Company: The Pepsi Bottling Group, Inc. Location: West Branch, MI Description: Operates equipment that blends raw materials to create beverage products to exact specifications. This includes weighing, measuring and mixing ingredients to standards. Performs routine tests to ensure resulting mixture meets specified properties and consistencies. Also includes periodic sampling of product as it is bottled/canned to ensure continued meeting of standards includes the product itself, fill levels, labeling, freshness dating and container integrity. Records test data and communicates modifications to the manufacturing process to eliminate any irregularities. May be required to periodically deep clean and sanitize blending/filling equipment and production lines. This job may require lifting/carrying cases weighing 20-45 pounds repeatedly over 10-12 hour period; and continuous standing and walking, manipulating and handling product samples while sitting PRIMARY ACCOUNTABILITIES: ? Operate and monitor line, removing or shifting materials and/or finished product as necessary to facilitate proper flow and machine operation ? Perform tests and use special equipment to ensure package and product quality ? Operate all manufacturing equipment efficiently and safely ? Clean equipment and area during and after shift ? Maintain clean work area through good housekeeping practices ? Expedite quality concerns to line; working with maintenance as necessary ? Keep daily records tests performed and results

Job Title: Quality Control Technician Company: The Pepsi Bottling Group, Inc. Location: Benton Harbor, MI Description: Operates equipment that blends raw materials to create beverage products to exact specifications. This includes weighing, measuring and mixing ingredients to standards. Performs routine tests to ensure resulting mixture meets specified properties and consistencies. Also includes periodic sampling of product as it is bottled/canned to ensure continued meeting of standards includes the product itself, fill levels, labeling, freshness dating and container integrity. Records test data and communicates modifications to the manufacturing process to eliminate any irregularities. May be required to periodically deep clean and sanitize blending/filling equipment and production lines. This job may require lifting/carrying cases weighing 20-45 pounds repeatedly over 10-12 hour period; and continuous standing and walking, manipulating and handling product samples while sitting PRIMARY ACCOUNTABILITIES: ? Operate and monitor line, removing or shifting materials and/or finished product as necessary to facilitate proper flow and machine operation ? Perform tests and use special equipment to ensure package and product quality ? Operate all manufacturing equipment efficiently and safely ? Clean equipment and area during and after shift ? Maintain clean work area through good housekeeping practices ? Expedite quality concerns to line; working with maintenance as necessary ? Keep daily records tests performed and results

Job Title: SE30 - Quality Control Technician Company: KSR Location: Troy, MI Description: Kelly Scientific Resources is seeking experienced Compliance Specialist to work a short term assignment at a global pharmaceutical company. This position will provide compliance assurance through the review of records to include batch documentation, training records, calibration records, standard operating procedures, regulatory policies, testing and manufacturing specifications, validation documents, and other technical documents; leading investigations, initiating deviations and determining corrective action. As a member of the Value Stream Packaging & Logistics team, be co-responsible for the site and the department results. Ensure personal objectives are aligned with site goals and objectives.PRINCIPLE JOB DUTIES:· Lead cross functional team to investigate deviations. Prepare reports from outcome of investigations.· Perform root cause analysis, FMEA’s and collaborates with the Industrial Excellence team to use other tools to address manufacturing concerns.· Review and assemble batch documentation testing results, training records, calibration records, standard operating procedures, regulatory policies, testing and manufacturing specifications, validation documents, and other technical documents.· Assess the impact of discrepancies on products or processes and recommend product disposition.· Determine robust corrective actions and/or commitments.· Ensure timely completion of manufacturing discrepancy commitments. This includes writing, revising, or coordinating the efforts for change controls, standard operating procedures, batch documentation and training documentation.· Initiate manufacturing deviations using a qualified system such as SAP.· Track, trend, and evaluate manufacturing discrepancies and work to determine root causes. This includes tracking and trending using a visual factory.· Prepare and track change controls to make improvements outside of deviations.· Maintain and track the CAPA’s for the manufacturing department.· Interact and coordinate with appropriate personnel including manufacturing, QA/QC, regulatory, technical services, etc.· Communicate immediately with QA and Operations management for all manufacturing discrepancies that impact product quality or safety.· Develop internal audit schedule (including area to be audited) on a yearly basis and communicates the schedule to the site Quality organization. · Write clear concise summaries of investigations, product impact assessments, and commitments.· Represent the manufacturing department at the site change control meetings.· Participate in the Process Qualifications during the start-up phase to support any deviations that are generated.· Interact with external regulatory authorities as needed during routine and non routine audits.· Provide classroom training to manufacturing operations as requested.· Participate in site Industrial Excellence initiatives.· Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practice. Adhere to all ?xml:namespace prefix="" st1 ns="urn:schemas-microsoft-com:office:smarttags" />GSK safety guidelines and procedures.· Adhere to all Quality Management System (QMS) policies and procedures as applicable for functional area. PRINCIPLE JOB DUTIES CONTINUED:· Cost: Demonstrate a cost conscience mindset and reduce waste in order to deliver profitability. · Reporting: Ensure that all relevant information relating to all functional responsibilities and activities are tracked, captured and forwarded in due time to the management.· Quality: Ensure all activities are executed following quality and regulatory standards. Promote a quality mindset and quality excellence approach to all activities. · EHS: Ensure all activities are executed including EHS standards and promotes a safety culture. · Act as change agent: Personal responsibility for supporting the value stream way of working at the site. Ensure that communication flows cross-functionally and that a purely functional focus (silo) is not allowed to develop. Deal positively with change, demonstrating the ability to maintain high personal performance levels as the organization evolves. Is also a positive influence on others' ability to adapt to change. Service to other Areas/Departments/Teams: Actively apply customer relationship management to provide pro-active response to customer needs. Maintain, develop and work in close relationship with all defined customers of the role. CANDIDATE SPECIFICATIONS:· B.S or B.A in a technical discipline, preferrably Microbiology, Biology/Virology, Biochemistry, Chemistry or Pharmacy. Degree in other discipline if sufficient technical depth has been achieved from profressional experience.· Minimum of 3 years pharmaceutical experience investigationg manufacturing deviations either in a QA or manufacturing role; preferrably in Biologics Secondary Manufacturing.· Working knowledge of pharmaceutical facilities, equipment and systems. Including a technical understanding of industry and science practices related to the business in order to apply knowledge to daily activities.· Demonstrated problem solving and investigational skills.· Knowledge of GMP’s, NIH Guidelines, FDA and other regulatory agency requirements sufficent to apply to quality operations and compliance.· The ability to commuincate both verbally and in writing with all levels both inside and outside of the oragniziation. The ability to clearly write technichal documentation as necessitated by regulatory agancies an internal policy.· Ability to establish and maintain working relationships with staff and the abiliy to analyize data and implement changes. · Able to interact with peers, subordinate and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production and QA. Ability to work in a high complex matrix environment.· Able to prioritize and decide appropriate course of actions and to effectively implementing decisions.· Ability to facilitate and generate the exchange of ideas to resolve problems, prioritize solutions, select optimal solutions and implement decisions.· Able to maintain attention to detail while executing multiple tasks.· Able to perform job duties with minimal supervision.· Sense of urgency, flexibility and accountability.· Intermediate computer skills required.· Stay current on developments in the field and-Bio Standards.Demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines. This position is 1st shift, short term ( 3 months and will run through the end of April) with a competitive pay rate. APPLY TODAY!!!

Job Title: Quality Control Technician Company: The Pepsi Bottling Group, Inc. Location: Kalamazoo, MI Description: Operates equipment that blends raw materials to create beverage products to exact specifications. This includes weighing, measuring and mixing ingredients to standards. Performs routine tests to ensure resulting mixture meets specified properties and consistencies. Also includes periodic sampling of product as it is bottled/canned to ensure continued meeting of standards includes the product itself, fill levels, labeling, freshness dating and container integrity. Records test data and communicates modifications to the manufacturing process to eliminate any irregularities. May be required to periodically deep clean and sanitize blending/filling equipment and production lines. This job may require lifting/carrying cases weighing 20-45 pounds repeatedly over 10-12 hour period; and continuous standing and walking, manipulating and handling product samples while sitting PRIMARY ACCOUNTABILITIES: ? Operate and monitor line, removing or shifting materials and/or finished product as necessary to facilitate proper flow and machine operation ? Perform tests and use special equipment to ensure package and product quality ? Operate all manufacturing equipment efficiently and safely ? Clean equipment and area during and after shift ? Maintain clean work area through good housekeeping practices ? Expedite quality concerns to line; working with maintenance as necessary ? Keep daily records tests performed and results

Job Title: Quality Control Technician - Carrollton, TX Company: KSR Location: Troy, MI Description: Kelly Scientific Resource is recruiting a Quality Assurance Technician for our client in Carrollton, TX. The QA Technician will review production batch files for accuracy and completeness and obtain corrections prior to acceptance of sub-assemblies, products or components. In addition, the Technician will perform audit, sampling, inspection, testing and identification of in-process materials, and complete required documentation in order to perform the final release of finished goods. The qualified candidate will have previous work experience in a food manufacturing, personal care or cosmetic manufacturing facility following GMPs and FDA regulations. Bi-lingual is a plus. This is a M-F day shift position. Pay is 14/hr.Kelly Scientific Resources is recognized as the world leader in the scientific staffing industry. Our recruiters are scientists themselves with prior industry experience. We offer a competitive benefit package including access to individual health plans and a retirement savings program. We provide scientific staffing services on a temporary, temp to hire, and full-time basis to a broad spectrum of industries including Chemical, Environmental, Food Science, Pharmaceutical, and Biotechnology.

Job Title: CR73 - Clinical Research Quality Control Specialist Company: KSR Location: Troy, MI Description: Every day, Kelly Scientific Resources (KSR) connects scientific professionals with opportunities to advance their careers. KSR is the first and largest scientific staffing company in the world, and we currently have an exciting direct hire Quality Improvement Specialist position available in the Milwaukee, Wisconsin area.By working with Kelly Scientific Resources, you will receive:- Competitive pay- Eligibility to a comprehensive benefits package- Access to the Kelly Science Learning Center- The opportunity to gain experience and references at one of the world's foremost pharmaceutical companies- And more!PurposeImplement and support the Quality Improvement Program activities for all human subject research approved by the IRBs to promote the conduct of research in a safe and ethical manner compliant with regulatory requirements, state law, and institutional policy and Good Clinical Practice guidelines.Essential Duties1. Perform Routine Reviews of human subject research approved by the IRB to ensure compliance with regulatory requirements, state law, and institutional policy and Good Clinical Practice guidelines.2. Record and report findings to designated individuals verbally and in writing.3. Assist the Program Coordinator III in the conduct of For Cause Audits.4. Provide consultation in creating and managing quality assurance/quality improvement measures for research investigators and research team members.5. Collaborate with staff of Quality Improvement and IRB in the development and provision of educational offerings to facilitate the conduct of ethical and complaint human subject research.6. Maintain records of reviews and activities.7. Provide technologic support in the maintenance and further development of QI database. Qualifications: Education: Bachelor’s degree in related science field required; Master’s degree in related field preferred.Experience: Minimum of 3 years experience in human subject research – coordinating, managing, reviewing, monitoring, auditing or providing quality assurance/quality improvement of human subject research. Previous experience in building, designing and/or maintaining Access databases.Certifications: Certification in human subject research preferred (CIP, CCRC, CCRA); ?or eligible for certification within 1 year of hire. Additional Knowledge/Skills:· Knowledge of federal and state regulations governing human subject research and Good Clinical Practice guidelines.· Knowledge of quality assurance/quality improvement principles and strategies.· Knowledge of adult education principles and strategies.· Proficient with Microsoft software.· Knowledge of database development and maintenance in various programs such as Access· Ability to maintain confidentiality.· Ability to solve problems logically.· Ability to work and communicate effectively with all levels of internal and external contacts.· Ability to communicate orally and in writing, clearly and logically.· Ability to meet deadlines without disruption to daily operations.· Ability to effectively plan and organize projects impacting the work of others.· Ability to manage multiple projects and maintain attention to detail.· Ability to effectively adapt to change. Kelly Scientific Resources® has grown into a $270 million global business as the scientific business unit of Kelly Services. We provide clinical research and scientific staffing to pharmaceutical, biotechnology, medical device and contract research organizations across the US. Kelly Services is an Equal Opportunity Employer.To be immediately considered for this position, click the 'Apply Now!' button. Or, refer a friend by clicking the 'E-mail this job' link provided.

Job Title: QA/QC Technician Company: Aerotek Location: Livonia, MI Description: Aerotek E&E is currently looking for someone with 2+ years of experience with QAQC Bituminous lab testing. This person will have a certification from MDOT through Ferris for Bituminous QAQC testing. They will be working in the lab performing tests on asphalt and coordinating with reporting authorities of the results. May have to go into the field on occasion to perform testing.