Sandoz Posted October 22, 2026

Manager GQS CSV & Digital Quality

Telangana, India Full time
Quality Manager
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About this opportunity

Job Description Summary

• Serve as a senior subject matter expert for Computerized System Validation (CSV), Digital Quality, Data Integrity, AI Governance and digital compliance across the Sandoz organization.

• Provide quality and compliance oversight for GxP computerized systems, digital platforms, data solutions, AI capabilities and automation technologies throughout their lifecycle.

• Support the implementation of Compliance by Design, Quality by Design, digital transformation and process simplification initiatives while ensuring alignment with applicable regulatory requirements and industry best practices.

• Partner with Quality, Digital and IT stakeholders to enable compliant, efficient and sustainable digital solutions across Development, Manufacturing, Quality, Supply Chain and Commercial functions.

Job Description

Position Purpose:

Serve as a senior subject matter expert for Computerized System Validation (CSV), Digital Quality, Data Integrity, AI Governance and digital compliance across the Sandoz organization. Provide quality and compliance oversight for GxP computerized systems, digital platforms, data solutions, AI capabilities and automation technologies throughout their lifecycle. Support the implementation of Compliance by Design, Quality by Design, digital transformation and process simplification initiatives while ensuring alignment with applicable regulatory requirements and industry best practices. Partner with Quality, Digital and IT stakeholders to enable compliant, efficient and sustainable digital solutions across Development, Manufacturing, Quality, Supply Chain and Commercial functions.

Your Key Responsibilities:

Your responsibilities include, but not limited to:

CSV & Digital Quality Oversight

Provide quality oversight and guidance for GxP computerized systems, digital platforms, data solutions, AI capabilities and automation technologies.

Support implementation and maintenance of CSV and Digital Quality frameworks, standards and procedures.

Ensure validation and compliance activities are conducted in accordance with applicable regulatory requirements and internal standards.

Contribute to regulatory inspections, audits and remediation activities related to computerized systems and digital solutions.

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Compliance & Risk Management

Support compliance with global GxP requirements, Annex 11, 21 CFR Part 11, Data Integrity principles, GAMP5, CSA and applicable AI regulations.

Perform risk assessments and support risk-based validation approaches for computerized systems and digital solutions.

Review validation documentation and ensure compliance throughout the system lifecycle.

Identify potential compliance gaps and support implementation of corrective and preventive actions.

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End-to-End Digital Quality Support

Maintain oversight of assigned digital solutions, computerized systems, interfaces and supporting processes.

Support lifecycle activities including requirements, validation, implementation, operation, monitoring, change management and retirement.

Drive standardization and harmonization of validation practices and digital quality processes.

Identify opportunities to improve compliance, efficiency and effectiveness through digitalization, automation and modern validation approaches.

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AI, Data & Automation Quality Assurance

Provide quality oversight for AI, Generative AI, advanced analytics and intelligent automation solutions used in GxP-relevant processes.

Support qualification, validation, monitoring and lifecycle management activities for AI-enabled solutions.

Assess compliance risks associated with digital innovations and recommend appropriate controls.

Support implementation of governance requirements for explainability, traceability and data integrity.

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Business Partnership & Project Support

Partner with Quality, Digital, IT and Business functions to ensure quality and compliance requirements are appropriately incorporated into digital initiatives.

Participate in project teams as Digital Quality subject matter expert.

Support deployment of new digital solutions and system enhancements.

Provide guidance and training on CSV, Digital Quality and Data Integrity requirements.

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Continuous Improvement & Knowledge Management

Monitor regulatory developments, industry trends and emerging technologies relevant to CSV and Digital Quality.

Support development and maintenance of standards, procedures, templates and best practices.

Contribute to inspection readiness, continuous improvement initiatives and knowledge-sharing communities.

Promote risk-based and pragmatic compliance approaches aligned with business objectives.

Key performance indicators:

Compliance & Inspection Readiness

Successful support of inspections, audits and compliance assessments.

Timely closure of digital quality observations and CAPAs.

Inspection readiness of assigned systems and digital solutions.

Digital Quality Excellence

Adoption of risk-based validation and CSA approaches.

Timely completion of validation deliverables and quality reviews.

Improved standardization and efficiency of validation activities.

Digital Transformation Support

Effective support of digital initiatives and system implementations.

Integration of Compliance by Design principles into project delivery.

Positive stakeholder feedback and business partnership.

AI & Digital Governance

Timely completion of AI and digital compliance assessments.

Effective support of AI governance requirements.

Sustainable implementation of compliant digital innovations.

What you’ll bring to the role:  

Essential Requirements:  

10-15 years of overall experience with significant experience in CSV, Digital Quality, IT Quality or GxP Compliance within the pharmaceutical industry.

Strong understanding of global regulations and Health Authority expectations governing computerized systems validation, lifecycle management, Data Integrity and 21 CFR Part 11 requirements.

Experience supporting development, implementation and lifecycle management of computerized systems in regulated environments.

Experience with Cloud, SaaS, digital and AI-enabled platforms used in GxP environments.

Experience with validation and quality oversight of systems such as SAP, ERP, Veeva, MES, LIMS, CDS and related platforms.

Understanding of AI, Generative AI and advanced analytics deployment within regulated environments.

Experience working in cross-functional and global project teams.

Experience supporting supplier qualification and computerized system compliance activities.

Strong communication, influencing and stakeholder management skills.

Proven ability to work independently, manage multiple priorities and deliver results in a complex matrix environment

Why Sandoz?

Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more, so that everyone can achieve the basic human right of access to good healthcare.

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.

Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!

Join us, help us make healthcare fairer and faster.

Commitment to Diversity & Inclusion: 

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Skills Desired

Agility, Business Acumen, Business Partnering, Collaboration / Teamwork, Communication Skills, Continued Learning, Dealing With Ambiguity, Decision Making Skills, Gmp Procedures, Goal-Oriented, Health Authorities, Leadership, Logical Thinking, Problem Solving Skill, Problem Solving Skills, Qa (Quality Assurance), Self-Awareness, Smart Risk Taking, Sop (Standard Operating Procedure)  , Technological Expertise

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Telangana, India
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 330 comparable Manager Quality roles across 80 biopharma companies.

330Comparable roles tracked
292Currently active
80Companies hiring similar roles
38Countries represented

Salary context

58 of 330 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate I, Quality Control, Raw Materials · ModernaTX, Inc. $53,500/yr – $85,600/yr
Highest disclosed · Advisor, Design Validation & Learning, Biotherapeutics · Lilly $168,000/yr – $268,400/yr
Peer group range $69,550 – $218,200 (median $167,850)

Where these roles are based

Top locations among the 330 comparable roles

United States137
India27
Ireland25
China23
Germany13
United Kingdom11

+ 32 more countries

Seniority mix

330 of 330 peers have a known seniority level

Manager219
Associate66
Associate Director45

Therapeutic area mix

1 of 330 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Respiratory1

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.

60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Bayer Bangalore, India Manager
Same function Same seniority Same country
60%similar
Teva Pharmaceuticals Mumbai, India Manager
Same function Same seniority Same country
60%similar
Pfizer Healthcare India Private Limited Vizag, India Manager
Same function Same seniority Same country

Notify me about similar jobs

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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.

60%
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Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
60%
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Function Therapeutic area Seniority Country
60%
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Novartis · Hyderabad (Office), India · Manager
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60%
Senior QA Manager ESO Biosimilars, LM
Sandoz · Telangana, India · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.