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Senior Scientist, Analytical Chemistry & Compliance

Job in Reading, Berks County, Pennsylvania, 19610, USA
Listing for: MSD Malaysia
Full Time position
Listed on 2026-07-27
Job specializations:
  • Science
    Pharmaceutical Science/ Research, Research Scientist, Analytical Chemist
Salary/Wage Range or Industry Benchmark: 117000 - 184000 USD Yearly USD 117000.00 184000.00 YEAR
Job Description & How to Apply Below
Senior Scientist, Analytical Chemistry & Compliance Skip to main content
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Hybrid locations:
USA
- Pennsylvania
- West Pointtime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
August 8, 2026 (14 days left to apply) job requisition :
R409334
** Job Description
** The Analytical Commercialization Technology (ACT) department within Analytical Chemistry in Development and Supply (ACDS) is seeking an applicant for a Senior Scientist position available at the West Point, PA site in the small molecule drug product Preliminary Stability Study testing laboratory.  The successful candidate will utilize analytical characterization technologies and compliance principles to drive method robustness and high-quality stability data in support of late-stage pharmaceutical drug product development and commercialization.  

The Senior Scientist responsibilities include, but are not limited to, stability sample analysis, leading analytical investigations in a cGMP environment, implementing new technology or continuous improvement measures for optimized laboratory operations, involvement in quality audits, and participating in or leading cross-functional compliance initiatives.  The successful candidate must have a proactive mindset and be able to collaborate in a dynamic, integrated, and multidisciplinary environment.
** Minimum

Education Requirements:

** Bachelor’s degree in Chemistry or related discipline with at least five (5) years of required experience and skills [Master’s degree with at least three (3) years] in the pharmaceutical industry.
** Required

Experience and Skills:

*** Familiarity with regulatory compliance principles [Good Manufacturing Practices (GMPs), Good Documentation Practices (GDPs)] and quality assurance practices related to analytical testing of pharmaceutical products.
* Strong background and hands-on experience with common analytical characterization techniques such as UPLC/HPLC, dissolution, and/or Karl Fischer titration.
* Demonstrated leadership skills and problem-solving abilities.
* Excellent verbal and written communication skills.
* Ability to work in a team environment with cross-functional interactions.
* Effective organizational skills and ability to manage competing priorities.
** Preferred

Experience and Skills:

*** Experience authoring deviations and investigations.
* Experience leading cross-functional teams.
* Experience mentoring others.
* Experience implementing digital tools in the workplace.
*
* Required Skills:

** Analytical Chemistry, Analytical Method Development, cGMP Regulations, Chemical Synthesis, Chromatography, Deviations, Flow Cytometry, Good Manufacturing Practices (GMP), Karl Fischer Titrations, Mass Spectrometry Based Proteomics, Mentorship, Pharmaceutical Development, Proper Documentation, Regulatory Compliance, Small Molecules, Spectroscopy
** Preferred

Skills:

** Current Employees apply HERE Current Contingent Workers apply HERE
** US and Puerto Rico Residents Only:
** Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please  if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and…
Position Requirements
10+ Years work experience
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