About Cardinal Health

Cardinal Health is a global, integrated healthcare services and products company connecting people, data, and technology to improve health outcomes. With over 48,000 employees worldwide, we provide pharmaceuticals, medical products, and services that enhance supply chain efficiency and patient care. Our Chemistry Services Center, part of QRMA Scientific Services, specializes in laboratory testing for medical devices and pharmaceutical stability, ensuring product safety and efficacy through advanced analytical techniques.

Role Overview

As a Scientist I, Pharmaceutical Analysts at Cardinal Health's state-of-the-art Scientific Service Center in Mansfield, MA, you will play a critical role in quality control for pharmaceutical products. This 100% onsite position involves reviewing stability test data, ensuring GMP compliance, and supporting regulatory requirements. Ideal for entry-level scientists with a passion for analytical chemistry and pharmaceutical quality assurance, this role offers hands-on experience in a cutting-edge lab environment focused on solid-dose pharmaceuticals and medical device characterization.

Key Responsibilities

In this position, you will:

• Provide thorough Quality Control review of pharmaceutical stability test data to verify compliance with quality standards.
• Analyze analytical data from tests like HPLC, GC, and dissolution, identifying deviations and investigating root causes.
• Ensure strict adherence to Good Manufacturing Practices (GMP), including SOP documentation and quality protocols.
• Review, approve, and manage stability studies, collaborating across departments to maintain product integrity and shelf-life.
• Conduct stability data trending, statistical analysis, and interpretation to predict degradation and shelf-life.
• Identify and report stability trends, deviations, or OOS results to QA leadership.
• Support change controls, stability study lifecycles, and preparation for regulatory inspections and audits.

Qualifications & Requirements

To succeed in this Scientist I role, candidates should have:

• A Bachelor's degree in chemistry or a related scientific field (preferred).
• 0-2 years of experience in pharmaceutical or biopharmaceutical quality control or testing.
• Strong knowledge of analytical techniques including HPLC, GC, UV-Vis, Karl Fischer, and dissolution.
• Familiarity with ICH guidelines, FDA regulations, data integrity, and Quality Risk Management.
• Working knowledge of method verification, validation, transfer, and OOS investigations (a plus).
• Experience with QMS (TrackWise, Veeva, Agile) and LIMS (LabWare) preferred.
• Excellent attention to detail, ability to prioritize multiple projects, and proactive mindset with minimal supervision.

Significant knowledge of USP, FDA, ICH requirements, GLP, and GMP is essential for maintaining compliance in stability testing.

Benefits & Perks

Cardinal Health offers competitive compensation estimated at $65,000-$95,000 annually, plus:

• Comprehensive medical, dental, and vision insurance plans.
• 401(k) retirement savings with generous company matching.
• Paid vacation, holidays, and flexible time off.
• Tuition reimbursement and professional development programs.
• Access to modern lab facilities and advanced instrumentation.
• Employee wellness programs and discounts on health products.

Career Growth

At Cardinal Health, your professional development is a priority. This entry-level Scientist I role provides a platform to build expertise in pharmaceutical analytics and quality assurance. With a structured Professional Development Plan, you'll gain exposure to regulatory affairs, advanced stability studies, and cross-functional collaboration. High performers advance to senior scientist or QA management positions within QRMA, leveraging our global network for long-term career progression in healthcare innovation.

Why Join Us

Join Cardinal Health in Mansfield, MA, to contribute to life-saving pharmaceuticals in a collaborative, innovation-driven environment. Our commitment to quality impacts millions through reliable medical devices and stable drug products. Enjoy a supportive culture emphasizing continuous improvement, work-life balance, and cutting-edge science. This onsite role at our West Building facility offers stability, growth, and the chance to make a tangible difference in patient health outcomes.

Role FAQs

Is this role entry-level?

Yes, it requires 0-2 years of experience, making it ideal for recent graduates with a chemistry degree.

What analytical skills are needed?

Proficiency in HPLC, GC, UV-Vis, Karl Fischer, and dissolution is preferred.

Is the position onsite?

Yes, 100% onsite at our Mansfield, MA facility.

What software experience is required?

Experience with QMS like TrackWise or Veeva and LIMS like LabWare is a plus.

How does Cardinal Health support regulatory compliance?

We emphasize GMP, GLP, ICH, and FDA guidelines, with training and tools for data integrity and audits.