Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

QC Analytical Chemist II

Job

DVM Manufacturing LLC

Malvern, PA (In Person)

Full-Time

Posted 2 weeks ago (Updated 1 week ago) • Actively hiring

Expires 7/12/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
62
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

QC Analytical Chemist II Malvern, PA 2 DAYS AGO 22637672 Summary Malvern, PA In-Person Competitive Salary 2 Years Experience Master's degree No Commission 40.00 hours per week / Day Shift / Full-Time Description Flamma
USA, LLC
seeks a QC Analytical Chemist II for its 383 Phoenixville Pike, Malvern, Chester County, PA 19355 location. As a QC Analytical Chemist II for a small molecule active pharmaceutical ingredient manufacturer and developer, the role will involve conducting GMP (Good Manufacturing Process) analyses on raw materials, in-process materials, final products, and stability samples. Also generating documentation to support the release of GMP materials. The QC Analytical Chemist II will participate in the development and validation of analytical methods and prepare related documentation. Additionally, will provide analytical support to the Process Research & Development (R D) group (Synthetic R D), collaborating on project advancements.
Primarily responsible for the following:
Calibrating, maintaining and operating laboratory equipment such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Gas Chromatography-Headspace analysis (GC-HS), Fourier Transform Infrared (FTIR) analysis, pH meter, balances, Karl Fischer (KF) titration, and Liquid Chromatography-Mass Spectrometry (LCMS); Conducting GMP analyses of raw materials, in-process materials, final product, and stability samples. Completing GMP documentation needed to support release of raw materials, intermediates, and final products. Validating methods for use in GMP environment. Preparing documents such as methods of analysis, specification, analytical reports, etc. Providing analytical support to Process R D (Synthetic R D) group and collaborating to advance the project. Participating in method development and optimization as necessary
Requirements:
Minimum of a Master's degree in Pharmaceutical Chemistry, Pharmaceutical Studies or a related field and at least 24 months of experience in the pharmaceutical industry, or related occupation. Must have at least twenty-four (24) months of experience with each of the following required skills: (1) Development, Validation, and Optimization of Analytical Method; (2) Method Validation Reports; and (3) Using instruments such as: High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Karl Fischer (KF) titration, pH meter, and Liquid Chromatography-Mass Spectrometry (LCMS). To apply, email HRFlammaUS@flammagroup.com Additional Details How To Identify Potential Job Scams