Associate Quality Control

Responsibilities

• Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
• Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
• Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations
• Operate laboratory equipment and instrumentation
• Performs review and approval of assays, documents and records
• Supports Continual Improvement initiatives
• Alerts management of quality, compliance, supply and safety risks
• Participate in laboratory investigations
• Performs general laboratory housekeeping activities
• Completes required assigned training to permit carry through of required tasks
• Performs additional duties as specified by management

Qualifications

• High school diploma / GED and 2 years of Quality or Operations experience OR
• Associates degree and 6 months of Quality or Operations experience OR
• Bachelors degree

Preferred Qualifications

• Professional work experience in a fast-paced, flexible GxP laboratory
• Demonstrated experience with various laboratory practices
• Self-motivated, strong organizational skills and ability to handle multiple tasks at one time with supervision
• Strong interpersonal skills (both written and oral), facilitation and presentation skills
• Demonstrate ability to be flexible and adaptable
• Knowledge of pharmacopeial testing, USP (United States Pharmacopeia) and PhEUR (European Pharmacopeia)
• Experience with benchtop wet chemistry (color change/precipitation reactions, titrations etc.) or HPLC/GC (high-performance liquid chromatography/gas chromatography) experience