(PRT) Senior CSV Manager
Há 1 mês
Time Type:
PLEASE REMEMBER TO CLICK "APPLY" BUTTON AFTER SAVING YOUR PROFILE TO COMPLETE YOUR APPLICATION PROCESS
DSV is on the lookout for a Computerised System Validation (CSV) Senior Manager to be a vital part of our IT Healthcare Center of Excellence team. If you thrive on navigating the dynamic landscape of CSV and are passionate about ensuring compliance with industry standards, then this is the opportunity you have been waiting for As a CSV Senior Manager, you will be at the forefront of implementing validation processes, keeping pace with industry regulations, and leading risk mitigation strategies. Your expertise will shape the future of DSV’s healthcare technology, and your contributions will resonate globally.
This is a permanent position within our Global IT organisation, with potential openings available in Denmark, Poland, Portugal, and India. If you are looking for a role where you can apply your skills and knowledge in a dynamic environment, we encourage you to apply.
As a CSV Senior Manager, You will:
Handle and monitor the implementation of validation protocols, guaranteeing accomplishment and documentation of validation actions in a timely manner
Focusing on Qualified Infrastructure in collaboration with our Enterprise Architecture department and other pertinent stakeholders
Stay updated on industry regulations, guidelines and best practices linked to CSV and incorporate them into the business's procedure
Perform risk assessments as well as offer leadership on risk mitigation methods linked to computerised systems
Write validation plans, IQ, OQ, PQ protocols and validation reports for multiple computerised systems
Evaluate and sign off on user requirement specifications, functional specifications and risk assessment connected to computerised systems
Work alongside cross-functional teams to outline validation needs for new equipment, systems and system upgrades
Other duties may be assigned
The Ideal Candidate:
Is educated to a degree level in a computer science, engineering, life science or similar discipline, though an advanced degree would be ideal
4 years of experience in Computer System Validation, preferably within the logistics or healthcare industry
Can Demonstrate experience within computerised systems validation in a regulated organisation such as pharmaceuticals, biotechnology, medical devices, etc.
Shows expertise in regulatory needs such as FDA, EMA, etc., as well as industry standards such as GAMP 5, 21 CFR Part 11, etc. connected to CSV
Shows leadership and project management abilities with the capacity to efficiently guide a team and handle various projects concurrently
Have excellent communication skills, both verbal and written
Is able to work effectively with others in cross-functional teams and regulatory agencies
Can familiarise with validation documentation, risk assessments, and validation implementation
Is fluent in the English language
What we offer:
Permanent contract (with basic salary in 14 installments per year)*
Private medical care
English courses - financial or co-financed by company
Food allowance (EUR 8.32, per working day)
Work schedule 35h/week
Hybrid and flexible work (3 days in a week at the office)
Comprehensive onboarding program
Buddy assistance
Good access to public transports
DSV – Global Transport and Logistics
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