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Quality Control Supervisor

2 months ago

Orange, California, United States BioPhase Solutions Full time
Job Overview

BioPhase Solutions is dedicated to connecting exceptional talent with the thriving Scientific sector in Southern California. We are currently seeking a QC Manager for a prominent cosmetic firm located in the Greater Los Angeles area.

Compensation: $90-110k

Key Responsibilities:
  • Oversee and manage the quality control operations to meet organizational goals.
  • Assess existing protocols and practices to enhance departmental effectiveness; initiate and execute necessary improvements.
  • Establish and maintain primary quality control systems in alignment with GXP (GMP, GLP, GCP) and SOPs.
  • Create and review protocols, reports, and SOPs; ensure compliance with product specifications and batch records.
  • Guarantee adherence to cGMP standards at all times.
  • Supervise product analysis in accordance with cGMP regulations and established SOPs.
  • Identify and resolve technical challenges.
  • Ensure proper documentation is completed to support testing processes.
  • Manage and oversee the department's budget.
  • Coordinate maintenance schedules for laboratory equipment; ensure compliance with GMP requirements and SOPs.
  • Participate in GMP audits.
  • Recruit, train, and lead quality control personnel; manage team schedules and workflow.
  • Delegate tasks and monitor work quality; ensure compliance with organizational policies and regulatory standards.
  • Stay informed about team activities, identifying issues and implementing corrective measures.
Required Qualifications:
  • Master's degree in a relevant field with a minimum of three years of experience, or a Bachelor's degree with at least five years of related experience.
  • In-depth knowledge of cosmetic manufacturing processes, equipment validation, GMPs, and product/process validation.
  • Comprehensive understanding of GMP, CFR, and compliance factors.
  • Ability to apply statistical methods for data evaluation.
  • Thorough familiarity with ISO 22716 regulations.
  • Experience in laboratory settings, including equipment and safety protocols.
  • Exceptional written and verbal communication skills.
  • Strong organizational, analytical, and problem-solving abilities.
  • Capability to prioritize tasks and manage workflow effectively.
  • Adaptability and a proactive approach to shifting priorities.