Biomarker Assay Specialist - Primary Care BU
appropriate level of assay validation. • Oversight of pharmacodynamic (PD) assay programs at contract Biomarker Assay Laboratories and delivery...
Bristol Myers Squibb - Devens, MA
BIOPROCESS SPECIALIST(Job Number:1201345)DescriptionWe are currently hiring for both day and night shifts. The hours for the night shift... (SOPs) and electronic work instructions. 8. Assists with the coordination and implementation of special projects such as validation or complex...
Bristol Myers Squibb - Devens, MA
BIOPROCESS SPECIALIST(Job Number:1201480)DescriptionBioprocess Specialists will work in teams and have continual interaction with members... instructions. 8. Assists with the coordination and implementation of special projects such as validation or complex investigations. 9. Revises...
Genzyme Corporation - Allston, MA
POSITION OVERVIEW/KEY RESPONSIBILTIES: The Validation Specialist I (VS-I) reports directly to the Manager of Validation. The VS... of the Engineering Validation Department is to provide documented evidence that the Performance Qualifications (PQ) of manufacturing equipment...
Software Validation Specialist II
PAREXEL International LLC - Billerica, MA
Software Validation Specialist II Department: Quality and Compliance Location: USA - Massachusetts - Billerica Employment Type: Full Time... implementation, computer systems validation (CSV) and ongoing support & maintenance activities related to systems used by PAREXEL staff in clinical trial...
Genzyme - Allston, MA
Title: Validation Specialist- Requal Location: United States-Massachusetts-Allston Other Locations: Genzyme has pioneered the development... RESPONSIBILTIES: The Validation Specialist I (VS-I) reports directly to the Manager of Validation. The VS-I will be responsible for performing validation...
Sanofi Group - Allston, MA
Title: Validation Specialist- Requal Location: United States-Massachusetts-Allston Genzyme has pioneered the development and delivery... Specialist I (VS-I) reports directly to the Manager of Validation. The VS-I will be responsible for performing validation in a GMP biotech...
Sanofi Group - Allston, MA
Title: Validation Specialist I Location: United States-Massachusetts-Allston One of the world's leading biotechnology companies... of the Allston Landing Facility. Validation Specialist I The Validation Specialist I (VS-I) reports directly to the Manager of Validation. The VS...
Sanofi Group - Cambridge, MA
Title: Validation Specialist I Location: United States-Massachusetts-Cambridge One of the world's leading biotechnology companies... (NYSE: SNY). The Validation Specialist I will perform a variety of moderately complex tasks and duties in support of Operations and Quality...
QA Validation Specialist Senior
Sanofi Group - Framingham, MA
Title: QA Validation Specialist Senior Location: United States-Massachusetts-Framingham One of the world's leading biotechnology... and Validation of Facilities, Utilities, Equipment, and Instruments, and related electronic systems to internal procedures, Standards, Practice documents...
Software Validation Specialist II
PAREXEL International LLC - Billerica, MA
Title: Software Validation Specialist II Department: Quality and Compliance Location: USA - Massachusetts - Billerica Employment Type: Full... implementation, computer systems validation (CSV) and ongoing support & maintenance activities related to systems used by PAREXEL staff in clinical trial...
Title: Validation Specialist I Location: United States-Massachusetts-Allston Other Locations: One of the world's leading biotechnology...: SNY). Validation Engineer I The Validation Engineer I (VE-I) reports to a Validation Engineer III or Manager of Validation. The...
Title: Validation Specialist I Location: United States-Massachusetts-Cambridge Other Locations: One of the world's leading biotechnology...: SNY). The Validation Specialist I will perform a variety of moderately complex tasks and duties in support of Operations and Quality Systems...
Title: Validation Specialist- Requal Location: United States-Massachusetts-Allston Other Locations: Genzyme has pioneered the development... RESPONSIBILTIES: The Validation Specialist I (VS-I) reports directly to the Manager of Validation. The VS-I will be responsible for performing validation...
QA Validation Specialist Senior
Title: QA Validation Specialist Senior Location: United States-Massachusetts-Framingham Other Locations: One of the world's leading... of Engineering and Validation of Facilities, Utilities, Equipment, and Instruments, and related electronic systems to internal procedures, Standards...
Title: Validation Specialist I Location: United States-Massachusetts-Framingham Other Locations: Genzyme has pioneered the development... commitment to improving the lives of patients. Learn more atwww.genzyme.com. The mission of the Validation Department is to provide documented...
Sanofi Group - Allston, MA
within regulatory filings, and during audits and inspections of the Allston Landing Facility. Validation Specialist I The Validation Specialist I (VS... is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY). The mission of the Engineering Validation Department is to provide documented...
Sanofi Group - Cambridge, MA
is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY). The Validation Specialist I will perform a variety of moderately complex tasks... to apply GMP validation principles in accomplishing project goals. The individual will execute predefined installation, operational, and performance...
Charles River Laboratories - Wilmington, MA
Validation Support Specialist Job ID: 120479 Location: USA - MA - Wilmington Full/Part Time: Full-Time Regular/Temporary: Regular Return... to Previous Page Responsibilities: Provide quality assurance monitoring and audits of all Charles River computer validation projects globally...
Research Specialist: Validation Study Methodologist
Institute's Research and Evaluation Group seeks to hire a Research Specialist with demonstrated experience developing and implementing complex... study. Qualified candidates will have demonstrated experience with the validation of quality measurement or other similar systems...