Job summary
Job post source
This job is directly from Cardinal Health
Job overview
The Scientist III, Pharmaceutical Analyst at Cardinal Health performs pharmaceutical stability testing and analysis to ensure product quality and regulatory compliance.
Responsibilities and impact
The role involves conducting analytical testing using HPLC, GC, UV-Vis, Karl Fisher, and dissolution testing, compiling and reviewing stability data, performing method validation and transfer, investigating out-of-specification results, and collaborating with cross-functional teams to communicate findings.
Compensation and benefits
The salary range is $104,700 to $149,600 with no bonus eligibility. Benefits include medical, dental, vision coverage, paid time off, 401k, health savings account, flexible spending accounts, disability coverage, paid parental leave, and wellness programs.
Experience and skills
Candidates should have a bachelor's degree in chemistry or related field with 4-8 years of analytical lab experience using pharmaceutical testing techniques and knowledge of regulatory guidelines such as ICH, USP, and FDA. Experience with quality management systems and LIMS is preferred.
Career development
The position includes mentoring junior team members and working with senior staff, offering opportunities to develop expertise in pharmaceutical stability testing and regulatory compliance.
Work environment and culture
Cardinal Health promotes an inclusive workplace valuing diversity and supports employees being their authentic selves, emphasizing collaboration and compliance with quality and regulatory standards.
Company information
Cardinal Health is a healthcare services company with a Scientific Services Center focused on quality, regulatory, and medical affairs, providing laboratory testing for medical device and pharmaceutical products.
Team overview
The candidate will join the Pharmaceutical Analysis Department within the Chemistry Services Center, working alongside lab managers and senior staff in a collaborative environment.
Job location and travel
This is a 100% onsite position at the Scientific Service Center in Mansfield, MA.
Application process
Applicants are encouraged to apply as soon as possible before the anticipated closing date of July 11, 2025, with submission of an application through the company's process.
Unique job features
The role involves working with state-of-the-art analytical instruments and software, adherence to cGMP and GLP standards, and participation in method validation and regulatory compliance activities.
Company overview
Cardinal Health is a global, integrated healthcare services and products company headquartered in Dublin, Ohio. It operates through two primary segments: Pharmaceutical and Medical. The Pharmaceutical segment distributes branded and generic pharmaceuticals, specialty drugs, and over-the-counter healthcare products, while the Medical segment provides medical, surgical, and laboratory products. Founded in 1971, the company has grown through strategic acquisitions, including the purchase of Kinray and AssuraMed. Cardinal Health generates revenue by supplying healthcare providers and pharmacies with essential products and services, leveraging its extensive distribution network and expertise in supply chain management.
How to land this job
Position your resume to highlight your expertise in pharmaceutical stability testing, specifically your experience with HPLC, GC, UV-Vis, Karl Fisher, and dissolution testing as these are core to the Scientist III role at Cardinal Health.
Emphasize your knowledge and application of cGMP principles, regulatory guidelines such as ICH, USP, and FDA, and your ability to perform method validation, verification, and transfer protocols, as these are key responsibilities.
Apply through multiple channels including Cardinal Health's official career site and LinkedIn to maximize your chances of being noticed for this onsite Mansfield, MA position.
Connect with professionals in Cardinal Health's Chemistry Services Center or QRMA Scientific Services division on LinkedIn; start conversations by referencing recent company innovations in pharmaceutical analysis or asking about team culture and challenges in stability testing.
Optimize your resume for ATS by incorporating keywords from the job description such as 'pharmaceutical stability testing,' 'analytical method validation,' 'cGMP,' 'HPLC,' 'FDA guidelines,' and 'data trend analysis' to ensure it passes initial automated screenings.
Use Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple relevant job portals, and find LinkedIn contacts to network with, allowing you to focus more effectively on preparing for interviews and skill development.
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