QC Manager

Job Description

Job Description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Manager to work for a leading Greater Los Angeles area cosmetic company.

Salary : $90-110k

Responsibilities :

• Directs and coordinates the activities of the quality control function to ensure achievement of company objectives.
• Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed.
• Develops and implements primary quality control systems consistent with GXP (GMP, GLP, GCP) and SOPs.
• Generates protocols, reports, and SOPs; reviews protocols, SOPs, product specifications, and batch records.
• Ensures that cGMPs are always met.
• Directs and coordinates analysis of products in compliance with cGMP regulations and SOPs.
• Identifies technical problems and develops solutions.
• Oversees completion of appropriate documentation to support testing procedures.
• Develops and maintains department budget.
• Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, GMP requirements, and SOPs.
• Participates in GMP audits.
• Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow.
• Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations.
• Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions.

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 and equipment 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 skills
• Strong organizational, problem-solving, and analytical skills
• Ability to manage priorities and workflow
• Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm

Please send resumes to [email protected] and visit our website at www.biophaseinc.com for additional job opportunities!!!