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- Tasks: Conduct stability testing and data analysis for pharmaceutical products using advanced lab techniques.
- Company: Join Cardinal Health, a leader in healthcare solutions dedicated to improving patient outcomes.
- Benefits: Enjoy medical coverage, paid time off, flexible spending accounts, and a 401k savings plan.
- Why this job: Be part of a dynamic team that values innovation and diversity while making a real impact in healthcare.
- Qualifications: Bachelor's degree in chemistry or related field with 2-4 years of lab experience preferred.
- Other info: This role is onsite in Mansfield, UK, and requires a work permit for non-residents.
The predicted salary is between 70000 - 90000 £ per year.
What Chemistry Services Center contributes to Cardinal Health
Chemistry Services Center perform laboratory testing to characterize the chemistries of our medical device products and stability testing for pharmaceutical products of Cardinal Health. Chemistry Services is a part of Quality, Regulatory & Medical Affairs (QRMA) Scientific Services. Under the umbrella of QRMA, Chemistry Services Center will use specialized instruments to perform Assay and impurity/degradant tests for stability program for solid dose pharmaceuticals.
This role is 100% onsite at our state-of-the-art Scientific Service Center in Mansfield, MA.
Responsibilities
As an experienced analytical chemist in Pharmaceutical Analysis Department, produces high quality data for pharmaceutical stability analyses.
Perform data compilation, review, evaluation and trend analysis on data as applicable.
Perform analytical testing on stability samples using various techniques like HPLC, GC, UV-Vis, Karl Fisher and dissolution testing to assess drug product stability.
Ensure accuracy and precision of analytical methods by adhering to established quality control procedures.
Ensure all stability testing is conducted according to cGMP principles.
Perform analytical method verification, validation and analytical method transfer protocols following the regulatory requirements (ICH, USP and FDA).
Perform investigations of Out of Specification (OOS) test results as needed follow FDA guidelines.
Maintain compliance with relevant regulatory requirements (e.g. ICH and FDA) related to stability studies and data documentation.
Communicate stability data findings to stakeholders through reports.
Qualifications
Bachelor’s degree in chemistry or a related scientific field, preferred or equivalent work experience.
2-4 years of analytical laboratory experience performing analyses using HPLC, GC, UV-Vis, Karl Fisher and dissolution testing to support pharmaceutical stability testing, preferred
Experience with commercial stability programs following ICH guidelines, preferred
Experience with analytical method verification and validation following regulatory guidelines, preferred
Experience with analytical method transfer following regulatory requirements such as USP , preferred
Experience with investigations of Out of Specification (OOS) per FDA guidelines, preferred
Knowledge of cGMP regulation/guidance.
Experience with pharmaceutical stability test analysis software and LIMS systems for data management, preferred
Experience with quality management systems (e.g., TrackWise, Veeva or Agile), experience with LIMS (e.g., LabWare) is a plus.
Proficient in the use of instrumental data systems, including data acquisition, analysis and processing (e.g., Waters’ Empower software and Mettler Toledo’s Labx) , preferred
Must be able to convey recommendations, data, observations, results, and problems accurately and effectively to co-workers, customers and management.
Ability to handle multiple projects, adhere to scheduled timelines while maintaining flexibility and attention to detail.
Good communication and interpersonal skills. Can operate independently with minimal guidance and supervision and a team player.
What is expected of you and others at this level
Produces high quality data and provides are able to provide interpretations of pharmaceutical stability analyses.
Experience with data chromatography acquisition software such as Waters Empower desired.
Experience with Quality Management Software (QMS), such as Trackwise, Veeva or Agile and Laboratory Information Management System (LIMS), such as LabWare.
Reports test data in a form and format that facilitates the use of the data by team members.
Work with lab manager and senior staff members of pharmaceutical analysis department, develops instrument testing protocol and methods, standard operating procedures (SOPs), work instructions and other instrument documentation.
Ensures that the necessary testing is performed according to the test specification, test method and to ensure testing is completed in a timely and efficient manner.
Work with senior chemists, participate in preparations of analytical method transfer and validation/verification protocols and reports.
Possesses working knowledge of USP, FDA and ICH regulatory requirements as applicable to pharmaceutical stability testing is desired.
Possess a thorough understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) to ensure compliance of systems and procedures.
Anticipated salary range : $80,500 – $92,500
Bonus eligible : No
Benefits : Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
Medical, dental and vision coverage
Paid time off plan
Health savings account (HSA)
401k savings plan
Access to wages before pay day with myFlexPay
Flexible spending accounts (FSAs)
Short- and long-term disability coverage
Work-Life resources
Paid parental leave
Healthy lifestyle programs
Application window anticipated to close: 1/2/2026 *if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
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Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.
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Scientist II Pharmaceutical Analyst employer: Cardinal Health
Contact Detail:
Cardinal Health Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Scientist II Pharmaceutical Analyst
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC, GC, and UV-Vis. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your suitability for the role.
✨Tip Number 2
Research Cardinal Health's Chemistry Services Center and understand their approach to pharmaceutical stability testing. This knowledge will help you tailor your responses in interviews and show that you're genuinely interested in the company and its work.
✨Tip Number 3
Prepare to discuss your experience with regulatory guidelines like ICH and FDA. Highlight any specific projects where you ensured compliance, as this is crucial for the role and will set you apart from other candidates.
✨Tip Number 4
Network with professionals in the pharmaceutical analysis field, especially those familiar with Cardinal Health. Engaging with current or former employees can provide valuable insights and potentially lead to referrals, increasing your chances of landing the job.
We think you need these skills to ace Scientist II Pharmaceutical Analyst
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in analytical chemistry, particularly with techniques like HPLC, GC, and UV-Vis. Emphasise any previous work with pharmaceutical stability testing and regulatory compliance.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention specific experiences that align with the job description, such as your familiarity with cGMP principles and your ability to conduct investigations of Out of Specification (OOS) results.
Highlight Relevant Skills: Clearly outline your skills related to data analysis, method validation, and quality management systems. Use examples from your past work to demonstrate your proficiency with software like Waters Empower and LIMS.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is accurate and presented professionally.
How to prepare for a job interview at Cardinal Health
✨Know Your Analytical Techniques
Make sure you are well-versed in the analytical techniques mentioned in the job description, such as HPLC, GC, and UV-Vis. Be prepared to discuss your experience with these methods and how you've applied them in previous roles.
✨Understand Regulatory Guidelines
Familiarise yourself with ICH, USP, and FDA guidelines related to pharmaceutical stability testing. Being able to demonstrate your knowledge of these regulations will show that you are serious about compliance and quality control.
✨Prepare for Data Analysis Questions
Expect questions about data compilation, review, and trend analysis. Have examples ready that showcase your ability to interpret data accurately and how you've used it to make informed decisions in past projects.
✨Communicate Effectively
Since the role involves communicating findings to stakeholders, practice articulating complex scientific concepts in a clear and concise manner. This will help you convey your recommendations and observations effectively during the interview.
