What are the responsibilities and job description for the Manufacturing and Formulations Associate position at Quality Chemical Laboratories?
Quality Chemical
Laboratories (QCL), a leading Pharmaceutical testing and manufacturing
laboratory in Wilmington, is seeking a qualified candidate for the position
of Manufacturing and Formulations Associate.
Minimum Requirements:
This position requires 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 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 SOP’s.
Perform other related duties, as required.
Report to the department Manager or Director, as applicable.
QCL offers competitive salaries commensurate with experience and an excellent benefits package as well as great potential for career advancement and leadership in a rapidly growing company.
Salary : $34,300 - $43,500