Overview
On Site
USD 177,500.00 - 186,000.00 per year
Full Time
Skills
Privacy
System testing
Regulatory Compliance
Pharmacy
RP
GxP
Data
Technical drafting
Computerized system validation
DSC
Standard operating procedure
GLP
Design
Risk assessment
Functional requirements
Traceability matrix
GAMP
Manufacturing
ROOT
Specification
Chromatography
Spectroscopy
HVAC
Corrective and preventive action
GMP
Preventive maintenance
Analytical skill
UV
FTIR
HPLC
EMS
Element management system
Good manufacturing practice
Art
Mapping
Personal Digital Assistant
Research and Development
Mergers and acquisitions
Job Details
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
External Takeda.com Ad Text
Takeda Development Center Americas, Inc. is seeking a Data Systems QA and Compliance Leader in Lexington, MA with the following requirements: B achelor's degree in Pharmacy or related field plus 4 years of related experience. Prior experience must include: Perform analytical method development (HPLC, UPLC) using reversed phase chromatography (RP) in regulated environment (GxP/GLP) using Agilent ChemStation and Waters Empower 2 and 3 Chromatography Data System (CDS) and drafting SOPs (procedures) thereof; draft and execute Computerized Systems Validation (CSV) for analytical instruments (ICP-MS, DSC,) and enterprise systems (Empower) in accordance with electronic records and electronic signatures regulations, including 21 CFR Part 11; author site-wide Standard Operating Procedures (SOPs) for calibration, preventative maintenance, and operation of agilent High Performance Liquid Chromatography (HPLC and UPLC) 1100/1260/1290 Systems using Waters Empower and Agilent Chemstation in regulated GLP environment; develop analytical and enterprise systems qualification protocols (including design, installation, operation and performance qualifications, risk assessment, validation plan, user requirements, functional requirement, traceability matrix) under GAMP (Good Automated Manufacturing Practice), electronic records and electronic signatures principles (21 CFR Part 11 and Annex 11) in commercial GMP environment; troubleshoot, root-cause analyze, and resolve issues with deviations and out-of-specification (OOS) analytical instruments (chromatography, spectroscopy), infrastructure (Environmental monitoring, HVAC, stability chambers, vaults, freezers, fridges) and continuing qualification (Temperature Mapping) and resolution of issues thereof in Corrective Action/Preventative Action Plans (CAPAs)/Effectiveness Checks (EC) while communicating to multidisciplinary teams, in commercial GMP environment; perform calibration and preventative maintenance on analytical instruments (Karl Fisher, Balances, pH meters, disintegrator, dissolution baths, UV/VIS, FTIR, HPLC, Dataloggers) and laboratory computerized systems (including Empower CDS, Rotronic EMS, Kaye LabWatch) in Commercial cGMP; draft responses to regulatory agencies queries including observations/483s and action plans based on the state of the art and regulations in the field (Temperature/Humidity Mapping and Monitoring guidance from WHO, ISPE, USP, FDA, PDA). Up to 20% domestic & international travel required for R&D quality functions and activities.
Full time. $177,500 - $186,000 per year.
Apply on-line at and search for Req #R0132042.
Locations
Lexington, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Description
External Takeda.com Ad Text
Takeda Development Center Americas, Inc. is seeking a Data Systems QA and Compliance Leader in Lexington, MA with the following requirements: B achelor's degree in Pharmacy or related field plus 4 years of related experience. Prior experience must include: Perform analytical method development (HPLC, UPLC) using reversed phase chromatography (RP) in regulated environment (GxP/GLP) using Agilent ChemStation and Waters Empower 2 and 3 Chromatography Data System (CDS) and drafting SOPs (procedures) thereof; draft and execute Computerized Systems Validation (CSV) for analytical instruments (ICP-MS, DSC,) and enterprise systems (Empower) in accordance with electronic records and electronic signatures regulations, including 21 CFR Part 11; author site-wide Standard Operating Procedures (SOPs) for calibration, preventative maintenance, and operation of agilent High Performance Liquid Chromatography (HPLC and UPLC) 1100/1260/1290 Systems using Waters Empower and Agilent Chemstation in regulated GLP environment; develop analytical and enterprise systems qualification protocols (including design, installation, operation and performance qualifications, risk assessment, validation plan, user requirements, functional requirement, traceability matrix) under GAMP (Good Automated Manufacturing Practice), electronic records and electronic signatures principles (21 CFR Part 11 and Annex 11) in commercial GMP environment; troubleshoot, root-cause analyze, and resolve issues with deviations and out-of-specification (OOS) analytical instruments (chromatography, spectroscopy), infrastructure (Environmental monitoring, HVAC, stability chambers, vaults, freezers, fridges) and continuing qualification (Temperature Mapping) and resolution of issues thereof in Corrective Action/Preventative Action Plans (CAPAs)/Effectiveness Checks (EC) while communicating to multidisciplinary teams, in commercial GMP environment; perform calibration and preventative maintenance on analytical instruments (Karl Fisher, Balances, pH meters, disintegrator, dissolution baths, UV/VIS, FTIR, HPLC, Dataloggers) and laboratory computerized systems (including Empower CDS, Rotronic EMS, Kaye LabWatch) in Commercial cGMP; draft responses to regulatory agencies queries including observations/483s and action plans based on the state of the art and regulations in the field (Temperature/Humidity Mapping and Monitoring guidance from WHO, ISPE, USP, FDA, PDA). Up to 20% domestic & international travel required for R&D quality functions and activities.
Full time. $177,500 - $186,000 per year.
Apply on-line at and search for Req #R0132042.
Locations
Lexington, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.