Database Administration Jobs in Juncos

Specialist QA with experience in the Medical Devices industry:Duties:Revision and approvals of technical documents like URS Design Report of technical data.Auditing Equipment/Facilities/Utilities of Qualification Protocols and execution.Commissioning and Qualification of Equipment/Sys More...

Specialist Quality Control with experience in: Method Transfers Technical Services expertise on NPIRequirementsDoctorate or Masters 2 years of directly related experience orBachelors 4 years of directly related experience orAssociates 8 years of directly related experience ORBiling More...

Method transfers and technical services expertise on NPIRequirementsDoctorate OR Masters 2 years of directly related experience OR Bachelors 4 years of directly related experience OR Associates 8 years of directly related experience OR High school/GED 10 years of directly related More...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on inciden More...

Experienced Quality Assurance Specialist with knowledge in: Commissioning and Qualification of Equipment/Systems/FacilitiesAuditing Equipment/Facilities/Utilities of Qualification Protocols and executionRevision and approvals of technical documents like URS Design Report of technical More...

Experienced quality assurance specialist.Commissioning and Qualification of Equipment/Systems/FacilitiesAuditing Equipment/Facilities/Utilities of Qualification Protocols and executionRevision and approvals of technical documents like URS Design Report of technical data.Deep knowledge More...

Experienced Quality Assurance Specialist with knowledge in:Commissioning and Qualification of Equipment/Systems/FacilitiesAuditing Equipment/Facilities/Utilities of Qualification Protocols and executionRevision and approvals of technical documents like URS Design Report of technical d More...

Quality Professional with Manufacturing Process Audit and Batch Record Review experience. Knowledge or to be familiar with DAI process PASx/MES application MAXIMO SAP and LIMS. Knowledge in tests (PH bioburden) chromatography deviations data analysis alarms. Available for non-sta More...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on inciden More...

Specialist QA with expertise in Quality Systems such as Deviations (Non-conformities CAPA and Change Control). Hands on experience in electronic systems for instance: Documentation platforms (CDOCS) Maximo Trackwise LIMS electronic batch record (MES) and SAP.  Experience with Val More...

Expertise in Quality Systems such as Deviations (Non-conformities CAPA and Change Control).Hands on experience in electronic systems for instance: Documentation platforms (CDOCS) Maximo Trackwise LIMS electronic batch record (MES) and SAPExperience with Validation of GxP applications More...

Experience performing Quality OversightSupporting Supply Chain & Incoming operations experienceMust be available from M-F 3rd shift 9:00 PM to 5:30 AMRequirementsDoctorate OR Masters 2 years of directly related experience Alternatively Bachelors 4 years of directly related exper More...

Specialist QA with expertise in Quality Systems such as Deviations (Non-conformities CAPA and Change Control). Hands on experience in electronic systems for instance: Documentation platforms (CDOCS) Maximo Trackwise LIMS electronic batch record (MES) and SAP. Experience with Validati More...

Specialist QA to perform Quality Oversight supporting Supply Chain & Incoming operations. Third Shift (9:00pm 5:30am) Monday - Friday Requirements Doctorate or Masters degree 2 years of directly related experience or Bachelor Degree 4 years of directly r More...

Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry Fully bilingual communications skills (English and Spanish) Good communications and presentation skills in English and Spanish Project management skills Strong organizational s More...