1 job found in wisconsin

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    • madison, wisconsin
    • temp to perm
    • US$22.00 - US$24.00, per hour, $22 - 24 per hour + none
    • 8:00 am - 4:30 pm
    Ensure that all aspects of product release meet analytical, production, packaging and labeling specifications in accordance with established quality systems. Support the maintenance, development and improvement of GMP quality systems, such as internal auditing, training, and documentation control.Responsibilities:Review and approve executed GMP batch documentationGenerate, review, and apply product labelsWrite and route operating procedures, manufacturing documents, and other QA controlled documents in QUMASInteract with internal customersSupport quality systemsIssue logbooksIssue/review controlled formsScan executed batch records and maintain electronic files for future reference as necessaryFile executed quality documentation in the records roomEnter data into multiple systems to ensure compliance with regulationsSupport SAP for the quality unitPerform walk-throughs, changeovers, and QA on the floor inspectionsProvide project support for QAServe as customer proxy for projects as assignedCreate and revise job aidesWorking hours: 8:00 AM - 4:30 PMSkills:General understanding of Q7 (current) Good Manufacturing PracticesGood computer skills, including proficiency MS Word, MS Excel, MS AccessGood time management skillsExcellent interpersonal skills for interacting with many internal departmentsAbility to organize and prioritize tasks effectivelyCapacity for independent workEducation:BachelorsExperience:ExperiencedQualifications:Education: Bachelor's degree with 0-2 years experience in GMP manufacturing, validation, QA, QC, or other functional area applicable to the job or an Associate's degree with 3-5 years applicable GMP experience in the specific QA job function as deemed appropriate by QA Management or at least 5 years experience with a degree not specified in a Life Science required. Please send updated resume to Rebecca.Ricksgers@external.milliporesigma.com or call my desk line at 951-514-4501. We look forward to hearing from you!Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    Ensure that all aspects of product release meet analytical, production, packaging and labeling specifications in accordance with established quality systems. Support the maintenance, development and improvement of GMP quality systems, such as internal auditing, training, and documentation control.Responsibilities:Review and approve executed GMP batch documentationGenerate, review, and apply product labelsWrite and route operating procedures, manufacturing documents, and other QA controlled documents in QUMASInteract with internal customersSupport quality systemsIssue logbooksIssue/review controlled formsScan executed batch records and maintain electronic files for future reference as necessaryFile executed quality documentation in the records roomEnter data into multiple systems to ensure compliance with regulationsSupport SAP for the quality unitPerform walk-throughs, changeovers, and QA on the floor inspectionsProvide project support for QAServe as customer proxy for projects as assignedCreate and revise job aidesWorking hours: 8:00 AM - 4:30 PMSkills:General understanding of Q7 (current) Good Manufacturing PracticesGood computer skills, including proficiency MS Word, MS Excel, MS AccessGood time management skillsExcellent interpersonal skills for interacting with many internal departmentsAbility to organize and prioritize tasks effectivelyCapacity for independent workEducation:BachelorsExperience:ExperiencedQualifications:Education: Bachelor's degree with 0-2 years experience in GMP manufacturing, validation, QA, QC, or other functional area applicable to the job or an Associate's degree with 3-5 years applicable GMP experience in the specific QA job function as deemed appropriate by QA Management or at least 5 years experience with a degree not specified in a Life Science required. Please send updated resume to Rebecca.Ricksgers@external.milliporesigma.com or call my desk line at 951-514-4501. We look forward to hearing from you!Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

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