Quality & Compliance Expert

Posted Yesterday
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Indianapolis, IN, USA
In-Office
82K-117K Annually
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Provide QA oversight for regulated IT systems, develop and revise CSV and GxP standards, gather global feedback, support IT4IT system validation and M&A activities, escalate non-compliance, partner with stakeholders to define product roadmap and governance, manage product lifecycle, and lead quality and compliance discussions.
Summary Generated by Built In

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

As part of the Quality Assurance team,  you will be a trusted partner for customers to ensure and improve the overall quality of IT systems throughout their lifecycle.  You are a customer-focused, highly collaborative individual who will work with delivery units across both Business and Informatics to advance existing and emerging business-critical technology according to Roche’s needs.

The Opportunity

You will ensure that Roche’s regulated/critical systems and services adhere to regulatory standards (e.g., CSV, GMP, GCP) and regulatory risks are managed adequately to protect Roche's business. By providing automated control insights and streamlined monitoring capabilities, an effective and consistent tracking of Information on Quality Oversight is enabled. Governance and processes are provided to comply with GxP,  Data privacy laws, and regulations when processing and hosting Roche data.

  • Participate in the development of new standards and the revision of existing standards related to Computer Systems Validation (CSV). 

  • Assemble global feedback on proposed or existing standards and tools and provide recommendations for new guidance/standards or revisions to existing guidance/standards.

  • Provide independent Quality Assurance oversight/support for IT4IT systems (and some business domains) with regard to Computer Systems Validation and other regulatory systems, including merger and acquisition activities.

  • Escalate non-compliance against quality standards to the appropriate governance bodies and Risk Management functions for resolution. 

 

STAKEHOLDER MANAGEMENT AND PARTNERING:

  • Connect and understand the regulatory and compliance needs in the context of the stakeholders and closely partner with them to develop the strategic direction of the product. Shape the Digitalized Compliance roadmap and portfolio to deliver high value outcomes for the customers of the product.

  • Define and deliver the product roadmap and manage the end-to-end product lifecycle (including continuously facilitating product discovery), ensuring it delivers tangible and meaningful value aligned with customer needs and expected business outcomes.

IMPACT AND COMPLEXITY

  • Define and manage product service levels, governance and operational support model aligned with stakeholder needs.

  • Lead or coordinate quality and compliance discussions for pragmatic solutions assuring a  quality is everyone’s responsibility mindset.

Who you are:

  •  You have a minimum of a Bachelor’s degree in Information Technology, Computer Science, Engineering, or equivalent.

  • You have a minimum of 5 + years of experience in information technology, data science, quality, or related professional competence. 

  • Exhibits a Lean-Agile Mindset and excels at Product Management practices. 

  • Takes 'progressive risk'--not thrill-seeking, but risk that leads to opportunity.

  • Has a keen Quality & Regulatory Expertise: You are passionate about major technology trends and continuously learning new capabilities (e.g. AI, Cloud, Data Meshes).

  • Demonstrates an executive presence, strong business acumen, ability to navigate ambiguity, and manages complexity.

  • Understanding of health regulatory frameworks (FDA, EMEA, ISO9001, ISO13485, PIC/s).

  • Understanding of risk and control frameworks and quality standards including government guidelines and laws (NIST, HIPAA, GDPR, EU AI Act).

 

Relocation benefits are available for this job posting.

Must be willing to work onsite in our Indianapolis, Roche location

The expected salary range for this position, based on the primary location of Indianapolis, is between $82,000 and $117,200. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.

Benefits

 

 

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.


Let’s build a healthier future, together.

Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Skills Required

  • Bachelor's degree in Information Technology, Computer Science, Engineering, or equivalent
  • Minimum of 5+ years experience in information technology, data science, quality, or related field
  • Experience with Computer Systems Validation (CSV) and GxP (GMP, GCP) compliance
  • Understanding of health regulatory frameworks (FDA, EMEA, ISO9001, ISO13485, PIC/s)
  • Understanding of risk and control frameworks and quality standards (NIST, HIPAA, GDPR, EU AI Act)
  • Lean-Agile mindset and strong Product Management practices
  • Demonstrated executive presence, business acumen, ability to navigate ambiguity and manage complexity
  • Willingness to work onsite in Indianapolis
  • Familiarity with IT4IT systems and providing independent QA oversight for IT services
  • Passion for and continuous learning of emerging technologies (e.g., AI, Cloud, Data Meshes)

Roche Compensation & Benefits Highlights

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

  • Retirement Support U.S. materials describe a 401(k) with both matching and an additional company contribution, supported by formal plan documents and true‑up features. This structure is positioned as a standout element of the total package, particularly at Genentech.
  • Leave & Time Off Breadth Time‑off provisions include substantial vacation, a year‑end shutdown, and a paid six‑week sabbatical after six years. These elements indicate a recharge‑oriented approach within the U.S. offering.
  • Healthcare Strength Company materials emphasize comprehensive medical, dental, vision, and mental‑health resources alongside well‑being programs. Benefits pages consistently highlight breadth across core health coverage elements.

Roche Insights

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The Company
Provincia de Buenos Aires
93,797 Employees
Year Founded: 1896

What We Do

Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. Thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry ten years in a row by the Dow Jones Sustainability Indices (DJSI).

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