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    1 job found for It in Raleigh, North Carolina

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      • Morrisville, North Carolina
      • Temporary
      • $23.00 per hour
      • 7:30 AM - 4:00 PM
      We are hiring a QA Specialist for a national biotech company located in Morrisville! It's a great opportunity to consider especially if you have experience in Quality Assurance within the medical device, biotech, or pharmaceutical industry.Responsibilities:- Performs inspection tasks by following established work instructions and procedures, by using required tools and methods and, when applicable, equipment, to determine acceptability of product, components, and documentation.- Performs pre-fill, in-process, and final inspections with the aid of documented work instructions and inspection information as required.- Stops production when a non-conformance (NCM) is observed and follows appropriate NCM procedures.- Documents non-conformances following applicable VWR Solon procedures and work instructions.- Documents and trends any quality production issues discovered during the course of inspection duties.- Ensures cleanliness of work areas during the inspection processes.- Utilizes problem solving tools such as 5M+E, 5 Whys, or other root cause analysis tools / methods to identify and permanently resolve issues.- Adheres to VWR Solons QMS and VWR Policies, where applicable.- Walks the floor to observe, train, and facilitate / support change.- Performs other duties as assigned.Working hours: 7:30 AM - 4:00 PMSkills:- Must be able to balance multiple tasks and prioritize efficiently- Knowledge of ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, ISO 17025, or EXCiPACT standard is preferred- Demonstrated experience or knowledge in conducting root cause analysis as it relates to nonconforming material investigations- Knowledge and experience utilizing Microsoft Outlook, Word, Excel, and Access, or equivalent software packages- Good communication skillsEducation:No Degree RequiredExperience:1-4 yearsQualifications:- High School completion or equivalent (GED) and a minimum of 3 years related experience and/or training in a regulated industry is required; OR Bachelors degree is required- Experience in a Quality Assurance role within the medical device, biotech, or pharmaceutical industry is preferred Apply online then call our office at 919-873-5588 and ask for Emily.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. 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.
      We are hiring a QA Specialist for a national biotech company located in Morrisville! It's a great opportunity to consider especially if you have experience in Quality Assurance within the medical device, biotech, or pharmaceutical industry.Responsibilities:- Performs inspection tasks by following established work instructions and procedures, by using required tools and methods and, when applicable, equipment, to determine acceptability of product, components, and documentation.- Performs pre-fill, in-process, and final inspections with the aid of documented work instructions and inspection information as required.- Stops production when a non-conformance (NCM) is observed and follows appropriate NCM procedures.- Documents non-conformances following applicable VWR Solon procedures and work instructions.- Documents and trends any quality production issues discovered during the course of inspection duties.- Ensures cleanliness of work areas during the inspection processes.- Utilizes problem solving tools such as 5M+E, 5 Whys, or other root cause analysis tools / methods to identify and permanently resolve issues.- Adheres to VWR Solons QMS and VWR Policies, where applicable.- Walks the floor to observe, train, and facilitate / support change.- Performs other duties as assigned.Working hours: 7:30 AM - 4:00 PMSkills:- Must be able to balance multiple tasks and prioritize efficiently- Knowledge of ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, ISO 17025, or EXCiPACT standard is preferred- Demonstrated experience or knowledge in conducting root cause analysis as it relates to nonconforming material investigations- Knowledge and experience utilizing Microsoft Outlook, Word, Excel, and Access, or equivalent software packages- Good communication skillsEducation:No Degree RequiredExperience:1-4 yearsQualifications:- High School completion or equivalent (GED) and a minimum of 3 years related experience and/or training in a regulated industry is required; OR Bachelors degree is required- Experience in a Quality Assurance role within the medical device, biotech, or pharmaceutical industry is preferred Apply online then call our office at 919-873-5588 and ask for Emily.Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. 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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