senior software developer.

job summary: Under the general supervision of the Supervisor of Client Engineering Desktop Supervisor, this position provides guidance and performs research for the management and administration of the Microsoft M365 application in the delivery of Microsoft solutions. This enterprise-wide responsibility includes the design and delivery of Microsoft solutions to meet business objectives, tenant technical requirements to create effective knowledge sharing, collaboration, and workflow solutions   location: MADISON, Wisconsin job type: Contract salary: $19 - 24 per hour work hours: 8am to 5pm education: Bachelors   responsibilities: Serving at the first point of contact for customers seeking technical assistance over the phone, email and through our ticketing system.Performing remote troubleshooting through diagnostic techniques and pertinent questions.Manage tickets assigned in a timely manner.Determine the best solution based on the issue and details provided by the customer.Develop/modifying Knowledge Base documentation.PC deployments, installation of software and assist customers with new devices.Record events and problems and through resolution logs. Requirements and Skills: 2-5 years experience working in a help desk environment.Proven experience with Microsoft Office, Teams and InTune services.In-depth knowledge of computer systems and mobile devices.Proven experience as a help desk technician.Ability to diagnose and resolve basic technical issues.Proficient with iOS and Android devices.Detail oriented and maintain confidentiality.Ability to work with minimal supervision.Customer-oriented and patient.   qualifications: Experience level: ExperiencedMinimum 3 years of experienceEducation: Bachelors  skills: Helpdesk Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: Randstad is the #1 HR Services Company in the world and we are sourcing for a QC Analytical Chemist in the Madison, WI area. The ideal candidate will provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $40,000 - 50,000 per year work hours: 11 to 7 education: Bachelors   responsibilities: Responsibilities: Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Analyzes pharmaceutical or cleaning samplesAbility to weigh samples, pipette, and prepare laboratory solutionsPerforms or assists with basic calibrationsMaintains a cGMP laboratory notebook, data, forms, and/or logbook.Assists in maintaining a clean, organized QC laboratory.Lifts/carries objects weighing up to 55 lbs.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: Bachelor's degree in Chemistry or related field.Experience with the use and troubleshooting of laboratory equipment desirable.Possesses good time management skills to complete assignments/projects in a timely manner with minimal supervision.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. Working Conditions The QC Analytical Chemist works in a cGMP laboratory and production environment. Working in these environments will require working near skin irritants, electrical equipment, sharp instruments, toxic materials, and hazardous chemicals including controlled substances. Safety procedures must be followed to limit exposure.   skills: Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory Practice), Laboratory Information Management Systems (LIMS), Sample Preparation, Sample Testing, Sanitation Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: Randstad is the #1 HR Services Company in the world and we are sourcing for a QA Associate in the Madison, WI area. The ideal candidate will provide quality assurance support and leadership to the Production Department. The QA Associate I, Process Quality Inspector provides a strong floor presence and works directly with production supervision and operators to maintain quality of manufacturing operations. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $35,000 - 43,000 per year work hours: 3 to 11 education: High School   responsibilities: Responsibilities: Works with Production personnel to ensure compliance of CPI practices, policies, and procedures. A significant focus on batch record and process compliance is expected. Performs routine review of in process production documents during processing to ensure accuracy and completeness.Performs routine inspections/audits on personnel, procedures, equipment, and products.Provides leadership to Production personnel on quality issues.Initiates deviations and documents initial investigations. May contribute to assessment of deviations under the direction of the supervisor.Contributes to quality investigations. Serves as lead investigator when assigned by the supervisor.Initiates, maintains, and dispositions non-conformances.Assists in training of Production personnel in company practices, policies, and procedures.Assists in the movement of controlled substances into/out of the controlled substance storage and processing areas.Performs sampling activities when assigned by the supervisor.Reviews unit logbooks and/or environmental monitoring data as assigned.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: High school diploma or equivalent required.2-3 years of industry quality or cGMP manufacturing experience required. Formal quality training may be substituted in place of experience.Knowledge of current Good Manufacturing Practices (cGMPs) preferred.Knowledge of a variety of cGMP manufacturing practices preferred (including fluid bed coating/granulation, capsule filling, milling, tableting)Strong attention to detail and problem solving skills required.Ability to read, write (legibly), and speak the English language at a level necessary for efficient job performance.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients.Ability to stand for extended periods of time and lift objects weighing up to 55 lbs.  skills: Quality control, SOP, Quality Assurance, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.