Manufacturing and Formulations Associate

About the Role

Quality Chemical Laboratories (QCL), a leading pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for a Manufacturing and Formulations Associate position.

Requirements

Minimum requirements for this position include an Associate's degree or higher in a scientific or engineering discipline with 0 to 3 years of experience, or an equivalent combination of education and experience.

Responsibilities

• Assist in carrying out any GMP or R&D manufacturing operations.
• Assist in the management and handling of all GMP and R&D materials, including receiving material, performing required sampling, and maintaining records to ensure the timely retesting of materials.
• Assist in all cleaning activities.
• Perform evaluations including but not limited to Powder Characterizations (Density, Particle Size, Flodex).
• Perform evaluations including but not limited to Tablet Characterizations (weight, thickness, hardness, friability).
• Assist in equipment installations and qualifications as needed.
• Perform viable and non-viable monitoring in the GMP Synthesis Clean Room and the Formulations GMP areas.
• Maintain strict client confidentiality.
• Work with the quality group to ensure compliance for all GMP work.
• Communicate daily with manufacturing and formulation management about work scheduling and project progress/results.
• Maintain training requirements on all necessary disciplines.
• Maintain adherence to safety standards as required by QCL SOPs.
• Perform other related duties as required.
• Report to the department Manager or Director, as applicable.