Senior Validation Lead – Systems & Compliance (Remote/Hybrid)

Bayer (Schweiz) AG; Poland; Hybrid; PLN 180,000 - 240,000; Full time

Benefits offered by this job

Flexible benefits

Insurance coverage (life/accident/dis/

Pension plan

Home office allowance

Extra paid holidays

Job summary

Bayer (Schweiz) AG is seeking a Sr. Validation Specialist to lead the validation of the Integration Mesh platform. You will develop validation plans for computer systems, ensure regulatory compliance, and guide junior team members in CSV documentation and lifecycle practices.

The role requires 7+ years in validation within pharma/medical devices, with hands-on work on platforms, APIs, and microservices. Strong communication is essential for cross‑functional collaboration and audits.

Qualifications

• Bachelor's degree in Computer Science, Technology, or a related field.
• 7+ years of validation of computer systems in pharma/medical device industries.
• Experience leading validation projects and teams.
• Strong IT background with platform engineering and microservices exposure.
• Ability to write validation plans and CSV-related documentation.

Responsibilities

• Lead validation work and the validation team for the Integration Mesh platform.
• Develop, review, and execute validation plans for computer systems per regulatory requirements.
• Collaborate with cross-functional teams to identify validation needs and ensure implementation.
• Create change requests and perform risk analyses for global/local systems.
• Guide team in lifecycle documents and validation SOPs; support audits.

Skills

Validation leadership

CSV documentation

API & messaging tech

AWS & Terraform

Node.js

GitHub

AI awareness

Communication skills

Education

Bachelor's degree in Computer Science/Technology/related field

Tools

AWS SQS

AWS Lambda

Terraform

Node.js

GitHub

Job description

Bayer (Schweiz) AG is seeking a Sr. Validation Specialist to lead the validation of the Integration Mesh platform. You will develop validation plans for computer systems, ensure regulatory compliance, and guide junior team members in CSV documentation and lifecycle practices.

The role requires 7+ years in validation within pharma/medical devices, with hands-on work on platforms, APIs, and microservices. Strong communication is essential for cross‑functional collaboration and audits.