Genentech

Quality & Compliance Expert

Genentech$82K — $117K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in IT, Computer Science, Engineering, or equivalent
  • 7+ years of experience in IT, data science, quality, or a related field
  • Exhibits a Lean-Agile Mindset with strong Product Management skills
  • Understands health regulatory frameworks (FDA, EMEA, ISO9001, ISO13485, PIC/s)
  • Has knowledge of risk and control frameworks and quality standards (NIST, HIPAA, GDPR, EU AI Act)
  • Demonstrates an executive presence and strong business acumen

Responsibilities

  • Ensure IT systems comply with regulatory standards (CSV, GMP, GCP)
  • Develop and revise standards related to Computer Systems Validation (CSV)
  • Gather global feedback on proposed or existing standards and provide recommendations
  • Provide independent QA support for IT systems regarding regulatory compliance
  • Escalate non-compliance issues to governance and Risk Management
  • Collaborate with stakeholders to define strategic direction for the product
  • Manage product lifecycle and deliver value aligned with customer needs

Benefits

  • Opportunities for personal expression and open dialogue
  • Supportive and collaborative company culture
  • Access to ongoing learning and professional development
  • Work in the impactful biotech industry
  • Contribute to innovative healthcare solutions
Full Job Description
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

About Genentech

Genentech is a biotechnology company that develops and manufactures drugs for the treatment of serious medical conditions. The company was founded in 1976 and is headquartered in South San Francisco, California. Genentech's products include treatments for cancer, multiple sclerosis, and other diseases. The company is a subsidiary of Roche, a Swiss pharmaceutical company. Genentech has been recognized for its innovative research and development, and has received numerous awards for its contributions to the biotechnology industry.
Learn more about Genentech
Size
14,000 employees
Industry
Founded
1976

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