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- Appleton, WI

Our client is a “Top 25” International Food Processing company that continues to grow. With this growth comes the need for a Quality Manager at one of their Midwest regional facilities. As the Quality Manager your expertise in the areas of Quality Systems and compliance will be essential parts of your responsibility. You will also be tasked to develop targeted strategic Quality initiatives to comply with the ever changing needs of the organization moving forward. Position reports to the VP of....

- Milwaukee, WI

Our client is a Top 25 International Food Processing company that continues to grow. With this growth comes the need for a Quality Analyst at one of their Midwest regional facilities. As the Quality Analyst your expertise in the areas of Quality Systems and compliance will be essential parts of your responsibility. You will be responsible for food safety audits. Requirements:Bachelor’s Degree in Microbiology, Food Science or related field. Equivalent experience may be considered.2 years of....


Responsibilities:Managing the cleaning and sanitation operations, ensuring proper execution of sanitation activities;Ensuring that all sanitation SSOPs are properly implemented;Training all new sanitation personnel;Training all personnel in proper chemical usage and handling;Solving any concerns in regards to GMP, SSOP, SDS, and Process Control programs;Performing cleanliness inspections of the plant, stored equipment, and overall environment;Establishing and maintaining a Master Sanitation....


Growing food manufacturer offering upward mobility in a family-friendly environment. This is a night shift position. Responsibilities:Supervising employees on the night shift;Training employees for safety, GMPs, sanitary maintenance, etc.;Reviewing production and operating reports;Resolving or requesting services for operational, manufacturing, and maintenance problems;Monitoring quality control programs to maintain company and USDA requirements;Ingredient usage and all other departmental....


Global food manufacturer offering solid growth and upward mobility. This is a 3rd shift opportunity. Responsibilities:Managing the cleaning and sanitation operations, ensuring proper execution of sanitation activities on the 3rd shift;Ensuring that all sanitation SSOPs are properly implemented;Training all new sanitation personnel;Training all personnel in proper chemical usage and handling;Solving any concerns in regards to GMP, SSOP, SDS, and Process Control programs;Performing cleanliness....


Responsibilities for 3rd Shift Sanitation Supervisor:Manage cleaning and sanitation employees in a food manufacturing facility on the 3rd shift;Train new sanitation employees in proper cleaning SSOPs, chemical use and safety procedures;Ensure uniform pre-operational standards through inspection and training;Solve concerns in regards to GMP, SSOP, SQF, SDS, and Process Control programs;Inspect plant, stored equipment, and environment for cleanliness;Establish and maintain a Master Sanitation....


Our client is a leader in food processing, and has been in business for over 100 years. The company has seen net sales exceeding $1.5 billion. The community is within a day’s drive to Des Moines, Omaha, and Kansas City. Responsibilities of the Continuous Improvement Engineer:Leading Continuous Improvement projects or activities with plant management;Using CI and Lean tools and analytical skills to identify and prioritize CI projects;Coordinating cross-functional project groups including....


Global food manufacturer offering solid growth and upward mobility. This is a 3rd shift position. Responsibilities of the Sanitation Supervisor:Manage cleaning and sanitation employees in a food manufacturing facility;Train new sanitation employees in proper cleaning SSOPs, chemical use and safety procedures;Ensure uniform pre-operational standards through inspection and training;Solve concerns in regards to GMP, SSOP, SQF, SDS, and Process Control programs;Inspect plant, stored equipment, and


Responsibilities:Coding .NET application, ASP.NET, ADO.NET or Entity Framework and SQL Server;Assisting in logical and physical database design;Meeting project plan timelines and producing a high quality product;Participating in requirements gathering meetings and code review sessions;Solving business problems through technology.Education: 4-year degree in Computer Science is preferred. Required Skills:3+ years of experience coding .NET application, ASP.NET, ADO.NET or Entity Framework and

- Mason City, IA

Responsibilities:Conducting application and technical design engineering on new and existing products;Investigating and/or creating new product opportunities by working within the engineering team to the satisfaction of customer requirements;Reviewing drawings and sales order requirements;Running design calculations to ensure reliability in all products;Providing full technical assistance to Sales, QA, Purchasing and Manufacturing;Analyzing designs in regards to cost and function to offer best


Recording and tracking all open issues to closure;Reviewing and analyzing advanced quality planning documents and capability studies to identify and resolve issues during the development and launch of a new product;Performing technical and statistical investigations and analysis on production , quality, process, and equipment issues;Resolving issues related to dimensional and performance requirements;Providing assistance in processing and delivering prototype parts by ensuring that tools....

- Effingham, IL

Responsibilities:Promoting the product maturation phase of new launches (performance, dimensional, and appearance);Supporting development from prototype through manufacturing production stages;Ensuring that product design, manufacturing, assembly, and other problems are detected an resolved at the earlies stages of the product development cycle;Reviewing advanced quality planning documents, FMEAs, PDS, Process Flow Diagrams, Control Charts, Gage R&R studies, and capability....


Responsibilities:Recording and tracking all open issues to closure;Reviewing and analyzing advanced quality planning documents and capability studies to identify and resolve issues during the development and launch of a new product;Performing technical and statistical investigations and analysis on production , quality, process, and equipment issues;Resolving issues related to dimensional and performance requirements;Providing assistance in processing and delivering prototype parts by ensuring


Responsibilities:Leading and facilitating the activities required to resolve automotive parts warranty issues;Oversite of testing and analysis of defective products;Leading and facilitating cross-functional warranty investigation teams;Leading the review of reports on investigations and analysis of warranty claims issues;Conducting meetings to update management on warranty claims status and ensure timely implementation of required countermeasures;Developing and maintaining relationship with....

- Florence, AL

Responsibilities:Managing all advanced quality planning documents;Participating in quality planning activities including FMEAs, Process Flow Diagrams, Control Charts, and Gage R&R and capability studies;Reviewing and preparing documentation, AQP, customer documents, etc.;Traveling to customers’ facilities to participate in all phases of the customer’s launch activities;Performing technical and statistical investigations and analysis;Verifying countermeasures for customer complaints, the....

- outside of Wichita, KS

TITLE: Medical Technologist LOCATION: Outside of Wichita, Kansas Are you looking for a new position where you can live and work in a community that offers big city conveniences in a micropolitan atmosphere so you can have the best of both worlds. Would you be interested in working for a healthcare leader in the region? Would you like to live in an area that is affordable and has low crime? Do you like to have a work life balance and live in an area with beautiful scenery and friendly people....


The Quality Control Chemist (QCC) reports to Quality Control (QC) Management.The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation practices.The QCC will assist in evaluating new testing applications and instrumentation, either developing methods or adopting compendial methods. This person will aid in....

- Sioux Falls, SD

Join a leader in their industry Quality Manager Responsibilities Ensure that all quality goals met or exceed company and customer objectives Develop and mentor team consisting of quality auditors, quality technicians, quality supervisors, quality engineers, and warrantee representatives Set policy, strategy, and implementation of overall direction for all quality functions and programs, including design and quality assurance, product quality, supplier quality, product reliability and customer....

- Any US State

Our client needs a doctor with experience in oncology clinical drug development to serve as a medical monitor. Work is estimated to take 10 hours per week to start.RequirementsMedical Doctorate (MD) or equivalent5 years clinical drug development experience in oncologyPhase 1 and phase 2 studiesResponsibilities1. Available to clinical investigator sites as a go-to person in the US for checking eligibility2. Be responsible for interacting with sites on safety management of the study. This will....

- Pleasanton, CA

Our large drug/device combo client in Irvine, CA needs a temporary Regulatory Affairs Associate. This contract is estimated to last 12 weeks. This person will coordinate most aspects of company regulatory activities and may interface with domestic and international health authorities. Qualifications: - BS or BA degree, 1-3 years of experience in regulatory affairs. - Experience in a company start-up environment, preferably in medical devices or combination products. - Knowledge of FDA, CA-FDB,

61-80 of 334 results