AVAILABLE Computer Systems Validation Specialist CSV, IT Quality Management, Technical Writing, Project Quality Manager PQM, GxP, GMP, 21 CFR Part 11
Aktualisiert am 19.06.2024
Profil
Freiberufler / Selbstständiger
Remote-Arbeit
Verfügbar ab: 10.06.2024
Verfügbar zu: 100%
davon vor Ort: 40%
Computerized System Validation
Project Quality
IT Quality
IQ
OQ
PQ
GxP
KNEAT
HP ALM
AGILE methodology
21 CFR
SDLC
Test script
Good Documentation Practice
Risk Assessment
FMEA
IT Control Frameworks
SAP Validation
Acceptance Test
Good Manufacturing Practice
Installation Qualification
Technical Documentation
CSV

Einsatzorte

Einsatzorte

Basel (+75km)
Schweiz
möglich

Projekte

Projekte

1 year 7 months
2021-12 - 2023-06

Veeva Vault QMS and Spotfire Dashboard upgrades and enhancements validation

Technical Writer and CSV Engineer csv KNEAT Testmanagement ...
Technical Writer and CSV Engineer

Subprojects included Distribution, Product Quality Complaints, Late Case Reporting, Engineering Docs, Issue Escalation, Batch Disposition.

Utilized KNEAT for document creation, test script execution, discrepancy management, and reviews. Employed ServiceNow for application change Control management.

Veeva Vault
csv KNEAT Testmanagement QMS
Moderna
Basel

Position

Position

Since 2002, I've excelled in validating computer systems crucial for Pharma, Medical Devices, and Life Sciences, ensuring that GMP manufacturing systems and GxP environments comply with quality standards. Skilled in supporting regulated IT infrastructure and fostering collaboration with team cooperation of business leaders, process owners, and experts. Adept at supporting Projects whilst working close to customers.

Kompetenzen

Kompetenzen

Top-Skills

Computerized System Validation Project Quality IT Quality IQ OQ PQ GxP KNEAT HP ALM AGILE methodology 21 CFR SDLC Test script Good Documentation Practice Risk Assessment FMEA IT Control Frameworks SAP Validation Acceptance Test Good Manufacturing Practice Installation Qualification Technical Documentation CSV

Schwerpunkte

CSV
IT Quality
Validation
Technical Writing
Veeva Vault
KNEAT
HP ALM

Creation, review and approval of validation and project lifecycle documents

Managing the CSV aspects ensuring robust and defendable validation

Proficiency in refining existing documents to enhance their overall clarity and effectiveness

Coaching and supervising of testers in good documentation practices according to industry best practices.

Previously engaged in remote transactions to ensure compliance and generate test evidence through proficient English language conversion.

Branchen

Branchen

Computer Systems Validation in the following industries:

Pharma, Medical Device, Biotech, Life Sciences

Einsatzorte

Einsatzorte

Basel (+75km)
Schweiz
möglich

Projekte

Projekte

1 year 7 months
2021-12 - 2023-06

Veeva Vault QMS and Spotfire Dashboard upgrades and enhancements validation

Technical Writer and CSV Engineer csv KNEAT Testmanagement ...
Technical Writer and CSV Engineer

Subprojects included Distribution, Product Quality Complaints, Late Case Reporting, Engineering Docs, Issue Escalation, Batch Disposition.

Utilized KNEAT for document creation, test script execution, discrepancy management, and reviews. Employed ServiceNow for application change Control management.

Veeva Vault
csv KNEAT Testmanagement QMS
Moderna
Basel

Position

Position

Since 2002, I've excelled in validating computer systems crucial for Pharma, Medical Devices, and Life Sciences, ensuring that GMP manufacturing systems and GxP environments comply with quality standards. Skilled in supporting regulated IT infrastructure and fostering collaboration with team cooperation of business leaders, process owners, and experts. Adept at supporting Projects whilst working close to customers.

Kompetenzen

Kompetenzen

Top-Skills

Computerized System Validation Project Quality IT Quality IQ OQ PQ GxP KNEAT HP ALM AGILE methodology 21 CFR SDLC Test script Good Documentation Practice Risk Assessment FMEA IT Control Frameworks SAP Validation Acceptance Test Good Manufacturing Practice Installation Qualification Technical Documentation CSV

Schwerpunkte

CSV
IT Quality
Validation
Technical Writing
Veeva Vault
KNEAT
HP ALM

Creation, review and approval of validation and project lifecycle documents

Managing the CSV aspects ensuring robust and defendable validation

Proficiency in refining existing documents to enhance their overall clarity and effectiveness

Coaching and supervising of testers in good documentation practices according to industry best practices.

Previously engaged in remote transactions to ensure compliance and generate test evidence through proficient English language conversion.

Branchen

Branchen

Computer Systems Validation in the following industries:

Pharma, Medical Device, Biotech, Life Sciences

Vertrauen Sie auf Randstad

Im Bereich Freelancing
Im Bereich Arbeitnehmerüberlassung / Personalvermittlung

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Rufen Sie uns an +49 89 500316-300 oder schreiben Sie uns:

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