IT Quality Expert (Bangalore, Karnataka, IN)
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At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.
IT Quality Expert
Purpose
To ensure the quality and regulatory compliance of the computerized system, related IT operations and IT suppliers. The role supports validation and qualification activities throughout system maintenance and development, including change control, deviation management, periodic reviews, while maintaining audit readiness.
Scope
Contribute to the IT Management System maintenance and continuous improvement
Provide product management support for validation and qualification activities
Ensure IT supplier quality and compliance aligned with internal standards
Support audit readiness and remediation activities in IT environment
Operate in an international environment with cross-functional collaboration
Key Tasks
Prepare and maintain validation documentation, including validation plans, risk assessments, requirements traceability, and validation reports
Assess the validation impact of system changes and coordinate updates to affected deliverables
Prepare and review validation test cases and support controlled validation test execution
Support investigations of validation deviations and track related CAPA actions
Perform scheduled periodic reviews of validated systems
Collaborate with cross-functional teams to ensure compliant product development
Maintain audit readiness and provide evidence for audit scoping and planning
Proactively identify risks, evaluate audit and inspection findings, monitor remediation and action plans
Support Quality Assurance Agreements with suppliers.
Train teams on compliance and documentation standards.
Working Relations
Team members and Team Leader
System Owners, Process Managers, internal clients and cross-functional IT and non-IT teams, external IT Service Providers
Internal and external auditors
Qualifications
Soft Skills
Passion for quality, compliance, and technology
Attention to detail and focus on accuracy and completeness
Strong communication and collaboration skills
Ability to work across cultures and global teams
Strong organizational skills and ability to manage multiple tasks
Willingness to learn and develop skills
Ability to train and share knowledge with others
Hard Skills
University degree in IT, natural sciences, or related field
Approx 5 years of experience in computerized system validation (CSV) or IT Quality assurance for regulated industries
Knowledge of GxP environment, preferably in the GCP area, and risk-based validation practices
English proficiency at B2/C1 level
Advanced Microsoft Office skills (Excel, Word, PowerPoint)
Experience with software development, agile environment and digital collaboration tools (Teams, SharePoint, Jira, AzureDevOps)
Basic knowledge of document management and validation lifecycle systems
Familiarity with audit, risk, change, or deviation management (beneficial)
Exposure to Veeva Vault products, Clinical Data management systems, or cloud-based integration and data platforms is an advantage
YOUR APPLICATION Bayer is an equal opportunity employer that strongly values fairness and respect at work. We welcome applications from all individuals, regardless of race, religion, gender, age, physical characteristics, disability, sexual orientation etc. We are committed to treating all applicants fairly and avoiding discrimination.
Location: India : Karnataka : Bangalore || Poland : Pomorskie : Gdańsk Division: Enabling Functions Reference Code: 896276 Contact Us + 022-25311234
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1507 comparable Quality roles across 149 biopharma companies.
Salary context
263 of 1507 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1507 comparable roles
+ 47 more countries
Seniority mix
737 of 1507 peers have a known seniority level
Therapeutic area mix
3 of 1507 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.