Senior Analyst, Quality Systems

Posted 14 Days Ago
Be an Early Applicant
Minnetonka, MN
In-Office
78K-115K Annually
Senior level
Healthtech • Biotech
The Role
The Senior Analyst in Quality Systems drives quality intelligence through data analysis, improving the Quality Management System, ensuring compliance, and streamlining quality processes across multiple areas.
Summary Generated by Built In

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We look forward to discovering your talents.

Welcome to an inspired career.

At Halozyme, we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and constantly strive to do more. We embrace transformation and work hard to innovate for the future. We do this together, as One Team – we rise by lifting others up and believe in the power of working together for the collective win. That’s why we need you—to help us make a significant impact by taking on increasingly complex challenges, leaping beyond the status quo, advancing our mission and making our One Team culture thrive.

Join us as a Senior Analyst 1, Quality Systems, and you’ll be part of a culture that welcomes diversity, thinks differently to solve problems, works collaboratively as one team, and delivers meaningful innovations that impact people’s lives.

How you will make an impact

The Senior Analyst 1, Quality Systems supports the oversight and continuous improvement of our Quality Management System (QMS). This position focuses on leveraging data to drive quality intelligence—developing and standardizing key metrics, building dashboards, and performing trend and gap analyses to identify opportunities for improvement. Working across multiple quality system areas, including CAPA, Deviation, and Change Control, the Senior Analyst transforms complex data into actionable insights that enhance compliance, streamline processes, and strengthen overall quality performance.

In this role, you’ll have the opportunity to:

  • Support the maintenance and enhancement of the QMS to ensure compliance with cGMP, FDA, ISO, and other applicable standards
  • Collect, analyze, and interpret quality data to identify trends, gaps, and opportunities for improvement across a variety of quality system areas including CAPA, Deviation, and Change Control processes
  • Design, standardize, and monitor key Quality Metrics to measure system health and performance
  • Collaborate with MasterControl System Administrators to build and maintain interactive dashboards that provide leadership with real-time visibility into QMS performance and compliance indicators
  • Perform deep-dive statistical analyses to detect early signals of systemic issues and recommend proactive corrective actions
  • Lead or support continuous improvement initiatives to streamline workflows, reduce waste, and optimize quality processes based on data-driven insights
  • Oversee and compile data for Quality Metrics meetings and Management Review meetings to ensure accurate reporting and informed decision-making
  • Partner with quality teams, process owners, and leadership to communicate findings, influence decisions, and drive standardization and simplification
  • Present data insights and improvement recommendations to senior management in a clear, actionable format; build strong relationships across all organizational levels
  • Promote a culture of quality awareness and continuous improvement through data transparency and proactive problem-solving

To succeed in this role, you’ll need:

  • Bachelor’s degree in Biology, Chemistry, Pharmaceutical Sciences, or a related field required with 5+ years of experience in Quality Assurance or Quality Systems within a biotech, diagnostic, or therapeutic environment (An equivalent combination of experience and education may be considered)
  • Strong foundation in regulatory compliance and quality system processes (CAPA, Deviation, Change Control)
  • Deep understanding of FDA 21 CFR Part 820, Part 11, ISO 13485, and related regulations and standards
  • Proficiency in electronic Quality Management Systems (eQMS) such as MasterControl, Veeva or TrackWise
  • Skilled in data visualization and dashboard development In return, we offer you:
  • Full and comprehensive benefit program, including an Employee Stock Purchase Program and 401(k) matching.
  • Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs and tuition reimbursement.
  • A collaborative, innovative team that works as one to amplify your impact—on your career, the work you do and patients’ lives.

The most likely base pay range for this position is $78K - $115K per year. Several factors, such as experience, tenure, skills, and particular business needs, will determine an individual’s exact level of compensation. Base salary is only one element of employee compensation at Halozyme. Total compensation could include bonuses, sales incentives, and equity awards.

Halozyme, Inc. is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.

Accessibility and Reasonable Accommodations:

Halozyme is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans during our application process. If you need assistance or accommodation due to a disability, contact Human Resources at [email protected].

To view all our open positions, please visit our career page. Additionally, our benefit offerings can be found here.

Top Skills

Data Visualization
Electronic Quality Management Systems
Mastercontrol
Quality Management
Quality Metrics
Trackwise
Veeva
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The Company
HQ: San Diego, CA
393 Employees

What We Do

Halozyme is a biopharmaceutical company bringing disruptive solutions to significantly improve patient experiences and outcomes for emerging and established therapies. Halozyme advises and supports its biopharmaceutical partners in key aspects of new drug development with the goal of improving patients' lives while helping its partners achieve global commercial success. As the innovators of the ENHANZE® technology, which can reduce hours-long treatments to a matter of minutes, Halozyme's commercially-validated solution has positively impacted more than 400,000 patient lives via five commercialized products across more than 100 global markets. Halozyme and its world-class partners are currently advancing multiple therapeutic programs intended to deliver innovative therapies, with the potential to improve the lives of patients around the globe. Halozyme's proprietary enzyme rHuPH20 forms the basis of the ENHANZE® technology and is used to facilitate the delivery of injected drugs and fluids, potentially reducing the treatment burden of other drugs to patients. Halozyme has licensed its ENHANZE® technology to leading pharmaceutical and biotechnology companies including Roche, Baxalta, Pfizer, Janssen, AbbVie, Lilly, Bristol-Myers Squibb, Alexion and argenx. Halozyme derives revenues from these collaborations in the form of milestones and royalties as the company's partners make progress developing and commercializing their products being developed with ENHANZE®.

We are a diverse team, who are committed to bringing therapies and results to patients. It's not enough to be qualified and experienced at what you do, we are looking for people who believe in our mission and match our values.
We are building a company where people can pursue their career goals in a supportive and collaborative team environment. Visit www.halozyme.com/careers for more details.

We are Halozyme.

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