QC Manager

3 months ago


Orange County, United States BioPhase Solutions Full time
Job DescriptionJob DescriptionBioPhase 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 tiffany@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities
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