About our client : Our client is a dynamic company at the forefront of the beauty industry, committed to delivering high-quality, innovative cosmetic and personal care products. Their mission is to enhance beauty and confidence in our consumers through scientifically advanced and ethically formulated products.
SUMMARY : Manages and coordinates the activities and operations of Quality Control
department and staff.
DUTIES AND RESPONSIBILITIES :
- Directs and coordinates the activities of the quality control function to ensure
achievement of company objectives.
Evaluates current procedures and practices for accomplishing departmentobjectives; develops and implements improvements as needed.
Develops and implements primary quality control systems consistent with GxPGMP, GLP, GCP) and SOPs.
Generates protocols, reports, and SOPs; reviews protocols, SOPs, productspecifications, and batch records.
Ensures that cGMPs are always met.Directs and coordinates analysis of products in compliance with cGMP regulationsand SOPs.
Identifies technical problems and develops solutions.Oversees completion of appropriate documentation to support testingprocedures.
Develops and maintains department budget.Manages laboratory equipment maintenance schedules; ensures laboratoryequipment is maintained in accordance with established schedules, GMP
requirements, and SOPs.
Participates in GMP audits.Hires, trains, supervises, motivates, and develops quality control staff; managesschedules and workflow.
Assigns duties and monitors quality of work; assures staff conforms toorganizational policies and procedures and government regulations.
Keeps up to date on overall activities of the team, identifying problem areas andtaking corrective actions.
Perform other activities as required.QUALIFICATIONS :
M.S. in related field and minimum of three years related experience or B.S.in related field and minimum of five years related experience.
Strong knowledge of Cosmetic manufacturing processes, computer andequipment validation, GMPs, and product / process validation.
Thorough knowledge of GMP, CFR, and factors impacting compliance.Knowledge of and ability to utilize statistic in evaluation of data.Thorough knowledge of ISO 22716 regulations.Experience with laboratory environment, equipment, and safety procedures.Excellent written and oral communication skillsStrong organizational, problem-solving, and analytical skillsAbility to manage priorities and workflowVersatility, flexibility, and a willingness to work within constantly changingpriorities with enthusiasm
