Business Analyst Quality Control Solutions- CDS

Posted Yesterday
Sandoz, CA, USA
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Acts as the bridge between business and technology for global Quality Control systems. Responsibilities include gathering requirements, designing and implementing QC solutions, supporting validation and testing in GxP environments, documenting processes, improving QC operations, managing stakeholder relationships, supporting change and training, and contributing to technology strategy and roadmaps. The role requires experience with regulated pharmaceutical or manufacturing environments and laboratory systems such as LIMS, CDS, or LabX.
Summary Generated by Built In

Job Description Summary

We are seeking an experienced Quality Control Solutions Business Analyst to join the Quality Control Solutions Team within the Supply Chain, Manufacturing & Quality Technology organization. This role is critical to delivering Sandoz's Digital Quality Strategy, acting as the bridge between business and technology to drive the development, implementation, and continuous improvement of global Quality Control systems. The successful candidate will work closely with global stakeholders to translate business requirements into scalable digital solutions, enhance QC processes, ensure compliance within GxP environments, and support the rollout of innovative technologies across Technical Operations.

Job Description

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally.

 

Job Summary


We are seeking an experienced Quality Control Solutions Business Analyst to join the Quality Control Solutions Team within the Supply Chain, Manufacturing & Quality Technology organization. This role is critical to delivering Sandoz's Digital Quality Strategy, acting as the bridge between business and technology to drive the development, implementation, and continuous improvement of global Quality Control systems. The successful candidate will work closely with global stakeholders to translate business requirements into scalable digital solutions, enhance QC processes, ensure compliance within GxP environments, and support the rollout of innovative technologies across Technical Operations.


Job Responsibilities

  • Act as a trusted advisor, using data-driven insights to improve Quality Control processes, systems, and services globally.
  • Capture, analyse, and translate business requirements into functional specifications for global QC systems and applications.
  • Lead and support the delivery, enhancement, validation, and rollout of Quality Control technology solutions.
  • Partner with business and technology stakeholders to identify process improvements and implement best practices across QC operations.
  • Develop and maintain business process documentation, ensuring consistency, traceability, and compliance with regulatory requirements.
  • Support computerized system validation (CSV), testing activities, qualification processes, and GxP documentation requirements.
  • Contribute to change management, training, deployment planning, and business adoption of new technologies and system upgrades.
  • Support the Quality Control Solutions leadership team in defining technology strategy, roadmap development, and future system capabilities.

Essential Requirements

  • Minimum 5 years' experience within manufacturing, process, or pharmaceutical industries, with exposure to digital technologies and global business environments.
  • Minimum 3 years' experience delivering Quality IT projects and managing system implementations within regulated environments.
  • Proven experience in Computerized System Validation (CSV) and working within GxP-compliant environments.
  • Strong business analysis skills, including requirements gathering, process mapping, stakeholder management, and solution design.
  • Experience with Quality Control systems such as LIMS, CDS, LabX, or similar laboratory technologies.
  • Excellent analytical, communication, influencing, and presentation skills with the ability to engage senior stakeholders.
  • Strong understanding of system lifecycle management, testing, validation, and quality management practices.
  • Fluent English, with the ability to communicate complex technical and business concepts effectively.

Education

  • Bachelor's degree (or equivalent) in Computer Science, Management Information Systems, Information Technology, or a related discipline.
  • Relevant certifications in Quality Systems, Business Analysis, Project Management, or Computerized System Validation would be advantageous.


Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients 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, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported! 


#Sandoz



Skills Desired

Budget Management, Business Acumen, Performance Management, Planning, Risk Management, Service Delivery Management, Stakeholder Management, Waterfall Project Management

Skills Required

  • Minimum 5 years of experience in manufacturing, process, or pharmaceutical industries
  • Experience with digital technologies and global business environments
  • Minimum 3 years of experience delivering Quality IT projects and managing system implementations in regulated environments
  • Experience with Computerized System Validation and GxP-compliant environments
  • Strong business analysis skills, including requirements gathering, process mapping, stakeholder management, and solution design
  • Experience with Quality Control systems such as LIMS, CDS, LabX, or similar laboratory technologies
  • Excellent analytical, communication, influencing, and presentation skills
  • Ability to engage senior stakeholders
  • Strong understanding of system lifecycle management, testing, validation, and quality management practices
  • Fluent English
  • Bachelor's degree or equivalent in Computer Science, Management Information Systems, Information Technology, or a related discipline
  • Relevant certification in Quality Systems, Business Analysis, Project Management, or Computerized System Validation

Sandoz Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Sandoz and has not been reviewed or approved by Sandoz.

  • Healthcare Strength — Health, dental, vision, and prescription coverage are consistently described as core components across U.S. roles and materials. Feedback suggests the medical offering is broad and a standard pillar of the package.
  • Retirement Support — A 401(k) plan with a company match described as generous is commonly included for U.S. roles. This savings support is positioned alongside other primary benefits as part of total rewards.
  • Equity Value & Accessibility — Equity eligibility is noted for many positions and a global all‑employee share program is being introduced from 2026. These elements add upside beyond base salary and annual bonus.

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The Company
HQ: Basel
17,135 Employees

What We Do

Sandoz is the global leader in generic and biosimilar medicines. ​ ​Our Purpose is to pioneer access to medicines for patients globally. We are on a mission to drive innovation in the healthcare industry by freeing up resources sustainably and responsibly while continuing to address global health challenges such as antimicrobial resistance.​ We are present in more than 100 countries and our medicines serve some 500 million people every year. We have two main global businesses: Generics - divided between standard generics and complex generics - and Biosimilars.

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