The vision of Sombra Cosmetic, Inc. is to continue the heritage of our Company and be a premier American manufacturer of top-quality products. We dedicate ourselves to be the supplier of choice when our type of products is being sought. This vision will be accomplished by sharing the responsibilities of planning and decision making with all our employees. Sombra will strive to maintain the image it has developed over the many years with its suppliers, customers, employees and community as a company of excellence.

Sombra Cosmetics is seeking a detail-oriented and knowledgeable cGMP Compliance Officer to oversee and ensure compliance with current Good Manufacturing Practices (cGMP) within our organization. This role is crucial in maintaining regulatory adherence, implementing quality assurance protocols, and supporting continuous improvement initiatives. The Compliance Officer will work closely with production, quality control, and management teams to uphold industry standards and regulatory requirements.

Key Responsibilities

  • Develop, implement, and maintain cGMP compliance programs, policies, and procedures.
  • Conduct internal audits and inspections to ensure adherence to cGMP regulations and company SOPs.
  • Identify and address compliance risks, non-conformances, and deviations; coordinate corrective and preventive actions (CAPAs).
  • Collaborate with quality control, production, and other departments to maintain a culture of compliance.
  • Ensure all employees receive appropriate cGMP training and maintain up-to-date training records.
  • Review and approve batch records, SOPs, and documentation to ensure regulatory compliance.
  • Stay current with regulatory changes and industry best practices, providing updates and recommendations to management.
  • Assist in regulatory inspections, customer audits, and certification processes.
  • Maintain documentation and records in accordance with FDA and other regulatory requirements.

Qualification & Requirements

  • Bachelor's degree in a relevant field (e.g., Life Sciences, Chemistry, Engineering, or related discipline).
  • Minimum of 2-5 years of experience in a cGMP-regulated industry (pharmaceutical, biotechnology, food, or supplements manufacturing).
  • Strong understanding of FDA regulations, cGMP requirements, and industry standards.
  • Experience conducting internal audits and managing CAPAs.
  • Excellent attention to detail, organizational skills, and problem-solving abilities.
  • Strong communication and interpersonal skills for training and collaboration.
  • Proficiency in Microsoft Office Suite and documentation management systems.

Preferred Qualifications:

  • Experience in a small business or startup environment.
  • Certification in Quality Assurance or Regulatory Affairs (e.g., ASQ, RAPS).
  • Knowledge of additional compliance standards such as ISO 9001, HACCP, or FDA Part 111.

Benefits

  • Competitive salary based on experience.
  • Health, dental, and vision insurance.
  • Paid time off and holidays.
  • Opportunities for professional growth and development.

If you are passionate about compliance and quality assurance and want to make a
significant impact in a growing company, we encourage you to apply.

Job Type: Full-time
Pay: From $70,000.00 per year
Schedule:
• 8 hour shift
• Monday to Friday
Ability to Commute:
• Albuquerque, NM 87109 (Required)
Ability to Relocate:
• Albuquerque, NM 87109: Relocate before starting work (Required)
Work Location: In person