Chemist

Ferndale Pharma Group • Ferndale, MI

1d

About The Position

Carry out routine day-to-day quality control testing of raw materials, in-process samples, bulk samples, finished product samples and/or stability samples. Prepare solutions for testing and achieve familiarity with preparing solutions based on units of normality (N), molarity (M), %v/v, %w/w, %w/v, etc. Progress in understanding and use of basic instrumentation in the QC Laboratory used in the performance of their specific duties (e.g., RM testing, FP/Stability testing). Document all aspects of testing in the laboratory notebook. Maintain an organized and neat workspace. Learn and utilize the basics of cGMP (current Good Manufacturing Practices) and GDP (Good Documentation Practices). Familiarity with use of the electronic USP-NF and FLI’s document management systems. Develop meticulous documentation skills. Generate test reports for review and approval. Other duties as assigned by the Supervisor.

Requirements

• Knowledge of basic Chemistry is a must; elements, compounds, chemical classes, solutions, how to prepare solutions by Normality, etc.
• Solid grasp of math skills.
• Must possess or be able to acquire basic skills involved in the use of a computer, including familiarity with Microsoft Outlook, Word and Excel.
• Bachelor’s degree in Chemistry or closely-related field, or a combination of relevant education and experience.
• Please note- this position requires background checks and a pre-placement physical and 10-panel drug screen (includes testing for marijuana due to federal contracts).

Responsibilities

• Carry out routine day-to-day quality control testing of raw materials, in-process samples, bulk samples, finished product samples and/or stability samples.
• Prepare solutions for testing and achieve familiarity with preparing solutions based on units of normality (N), molarity (M), %v/v, %w/w, %w/v, etc.
• Progress in understanding and use of basic instrumentation in the QC Laboratory used in the performance of their specific duties (e.g., RM testing, FP/Stability testing).
• Document all aspects of testing in the laboratory notebook.
• Maintain an organized and neat workspace.
• Learn and utilize the basics of cGMP (current Good Manufacturing Practices) and GDP (Good Documentation Practices).
• Familiarity with use of the electronic USP-NF and FLI’s document management systems.
• Develop meticulous documentation skills.
• Generate test reports for review and approval.
• Other duties as assigned by the Supervisor.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level