Vakulatech

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Title: Principal Commissioning/Validation Engineer III Location: Framingham MA Duration: 06 months contract (Chances of extension) Requirements: BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience. Experience in pharmaceutical/biopharm More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Title: Principal Commissioning/Validation Engineer III Location: Framingham MA Duration: 06 months contract (Chances of extension) Requirements: BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience. Experience in pharmaceutical/biopharm More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Role : Manufacturing EngineerUrgent Location : Mounds view MN need candidate from Medical domain side Keywords : Risk assessment Labeling TMVProduction control CAPA DFMEA PFMEA IQ/OQ/PQ QSR 21 CFR 820 ISO 13485 ISO 14971 Track wise Job Description: Review and approve the More...

Role : Manufacturing EngineerUrgent Location : Mounds view MN need candidate from Medical domain side Keywords : Risk assessment Labeling TMVProduction control CAPA DFMEA PFMEA IQ/OQ/PQ QSR 21 CFR 820 ISO 13485 ISO 14971 Track wise Job Description: Review and approve the More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Title: Principal Commissioning/Validation Engineer III Location: Framingham MA Duration: 06 months contract (Chances of extension) Requirements: BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience. Experience in pharmaceutical/biopharm More...

Title: Principal Commissioning/Validation Engineer III Location: Framingham MA Duration: 06 months contract (Chances of extension) Requirements: BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience. Experience in pharmaceutical/biopharm More...

Role : Manufacturing EngineerUrgent Location : Mounds view MN need candidate from Medical domain side Keywords : Risk assessment Labeling TMVProduction control CAPA DFMEA PFMEA IQ/OQ/PQ QSR 21 CFR 820 ISO 13485 ISO 14971 Track wise Job Description: Review and approve the More...

Role: Quality Assurance (QA) Specialist Medical Device Manufacturing Location Pleasanton CA Duration: Long Term Contract Responsibilities: Minimum of 46 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation More...

Role : Manufacturing EngineerUrgent Location : Mounds view MN need candidate from Medical domain side Keywords : Risk assessment Labeling TMVProduction control CAPA DFMEA PFMEA IQ/OQ/PQ QSR 21 CFR 820 ISO 13485 ISO 14971 Track wise Job Description: Review and approve the More...

Job Title: Guidewire Business Analyst Location: San Antonio TX Rate: 4547$/Per Hour. Only W2 roleNo C2C. Job Description: Guidewire Claims Center Policy center business Analyst A Guidewire business analyst is expected to carry out the following Requirement Elicitation More...

Title: CSV Engineer Location: Rocky Mount NC Onsite Duration: 12 Months You will be responsible for Resolution of fundamental Computer System Validation compliance issues on assigned projects Writing reviewing and executing computer validation documentation Perform compute More...

Role: Java Frontend Developer Location: Fort Worth TX (Hybrid 2 days a week onsite) Duration: 1 Year Note: Looking for locals only Rate $55/HR on W2 Job Description: Mandatory : Strong Frontend Angular to Angular JS migration experience needed Need 10 Years exp Sr. Java Fronte More...