Senior Life Science Consultant - Senior Computer System Validation Consultant with AI Expertise

Johnson & Johnson; Berlin; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Senior Life Science Consultant with expertise in Computer System Validation and AI. This role involves consulting for clients in the pharmaceutical sector, focusing on validation processes and innovative AI solutions. You will leverage your experience to develop and implement robust testing strategies, ensuring compliance with regulatory standards. Join a dynamic team that values diversity and encourages professional growth while working on exciting global projects. If you are passionate about technology and quality assurance, this opportunity is perfect for you.

Leistungen

Flexible working hours

Home office options

Professional development and training

Competitive salary

Substantial bonus

People-oriented culture

Diversity and inclusion-focused environment

Global client projects

Flat hierarchies

Qualifikationen

• 3+ years in Computer System Validation and AI expertise.
• Experience in FDA regulated environments and GxP standards.

Aufgaben

• Provide consultation in computer system validation and AI solutions.
• Develop and maintain AI solutions using ChatGPT.

Kenntnisse

Computer System Validation (CSV)

AI Solutions

Open AI Technologies

FDA Regulations

GxP Standards

QA Methodologies

Communication Skills

Team Leadership

Ausbildung

Bachelor’s degree in Computer Science

Master’s degree in a related field

Tools

AI Testing Strategies

Test Plans and Scripts

Jobbeschreibung

Senior Life Science Consultant - Senior Computer System Validation Consultant with AI Expertise [Berlin, 10115], [Hessigheim, 74394], [Hamburg Hamburg-Altstadt, 20099], [Baden-Baden, 76530], [Bavaria, ], [Bremen, ], Baden-Württemberg, Bavaria, Bremen, Hamburg, Hesse, Berlin - Germany | Posted - 11 / 07 / 23 Overview

We are looking for enthusiasts

KVALITO Consulting Group is a strategic partner and global Life Science network for regulated industries withafocus on quality. Headquartered in Basel, Switzerland, we have subsidiaries in Germany, Czech Republic, Ireland, Italy, and Malaysia. With our enthusiasm for progressive technologies and our in-depth knowledge of industrybest practicesand regulations, we drive effective and efficient project delivery to keep our industry-leading clients ahead of the competition. Our leadership and consultants combine decades of experience in enterprise environments. To cover all essential technical areas in the field of digital and mobile, KVALITO works with reliable Technology Partners worldwide. For more information, please visit us atwww.KVALITO.ch

Senior Computer System Validation Consultant with AI Expertise

Only candidates located within the European Union (EU) will be considered for this position.

Duration : 6 months (withthe possibility of extension)

We are seeking a highly skilled and motivated senior CSV consultant with expertise in AI to join our team. The ideal candidate should have proven experience with system development, lifecycles, computer system validation, and regulatory standards. Additionally, the candidate should possess extensive knowledge of AL solutions, including using Open AI technologies like ChatGPT, and demonstrate the ability to develop robust testing strategies for these systems.

Responsibilities

• Providing consultation services to our clients in the pharmaceutical industry, with a specific focus on computer system validation (CSV) and AI solutions
• Develop, implement, and maintain AI solutions using technologies like Open AI's ChatGPT.
• Feed internal procedures & documents into AI systems, ensuring the system accurately identifies the source.
• Deliver insights on regulatory differences across various countries and present these findings through clear, concise reports and graphical representations.
• Develop and execute validation deliverables, including requirements, compliance / validation plans, test protocols, test summary reports, and compliance / validation reports.
• Review and approve system tests, user acceptance test scripts, traceability matrices, and design specifications.
• Design and understand test plans, system, and UAT test scripts, and test procedures for AI solutions.
• Guide validation, conduct timely reviews, and escalate to TQ management when necessary.

Minimum Qualification and Experience

Education

• Bachelor’s degree in computer science, Data Science, or a related field.
• Master’s degree is preferred.

Language

• Fluent in English (oral and written) is a requirement.
• Any additional language is plus.
• 3+ years of experience in Computer System Validation.
• 2+ years of experience with the System Development Lifecycle.
• Prior experience in the Pharmaceutical, Biotechnology, or Medical Device industry.
• Familiarity with FDA regulations and global regulatory environments.
• Understanding of GxP standards and risk-based validation.

Skills

• Experience in FDA and / or Global regulated environment with a good understanding of GxP standards and Risk-based validation.
• Proficient knowledge of FDA guidance and industry standards (i.e., GAMP).
• In-depth knowledge and practical experience with AI technologies, specifically Open AI's ChatGPT.
• Proven experience with AI testing strategies and understanding AI models.
• QA methodologies and the ability to design, review, and approve test plans, scripts, and procedures.
• Strong written and verbal communication skills
• Abilityto work as a team player, lead, or complete tasks independently.
• Strong attention to detail and ability to ensure data accuracy and reliability.
• Capability to work with remote teams and support multiple projects simultaneously.
• Exceptional organizational and multitasking skills.
• Proven ability to lead a team and work independently.

We offer great benefits

• Flat hierarchies and responsibility from the beginning
• People-oriented culture
• Diversity and inclusion-focused environment
• Global client projects in a multinational environment
• Flexible working hours and home office
• Individual professional development, training, and coaching
• Unlimited full employment contract
• Excellent remuneration package consisting of a competitive salary plus a substantial bonus.

Contact

If you have the necessary background and experience and would like to join a small team responsible for a truly global operation, then please send your application torecruiting(at)kvalito.ch including your :

• CV, cover letter, and supporting documents(i.e.,diplomas, certificates, references)
• Availability - earliest start date
• Salary expectations
• Location preference

We are looking forward to your application.