Senior Quality Manager (Consultant/Part Time)

Astrix; California; On-site; USD 125,000 - 150,000; Part time

Job summary

A leading company in IT Services and Consulting is seeking a Senior Quality Manager on a part-time basis. This role involves enhancing quality programs and procedures according to regulatory standards. The ideal candidate should have a minimum of 10 years in Quality Assurance, specifically in cGMP compliance, and provide leadership to team members.

Qualifications

• Minimum of 10 years of Quality Assurance experience, focusing on cGMP compliance.
• Proven track record in effective QA/QC compliance programs.
• Understanding of FDA guidelines and industry standards.

Responsibilities

• Design, implement, and enhance quality programs.
• Develop validation protocols for critical areas.
• Mentor QA and Production team members.

Skills

Quality Assurance

Problem Solving

Communication

Job description

Senior Quality Manager (Consultant/Part Time)

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Senior Quality Manager (Consultant/Part Time)

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• Design, implement, and enhance quality programs, policies, and procedures aligned with regulatory requirements and industry best practices.
• Develop and execute validation protocols for water systems, equipment, manufacturing processes, cleaning and sanitization (C&S), and other critical areas.
• Identify areas of non-compliance and implement corrective and preventive actions (CAPAs).
• Mentor and support QA and Production team members to build a culture of collaboration, continuous improvement, and compliance excellence.
• Perform other QA-related tasks as assigned, in support of overall quality objectives.
  
  

Part Time Quality Assurance Manager

$65-$75 per hour

Onsite to start

Key Responsibilities:

• Design, implement, and enhance quality programs, policies, and procedures aligned with regulatory requirements and industry best practices.
• Develop and execute validation protocols for water systems, equipment, manufacturing processes, cleaning and sanitization (C&S), and other critical areas.
• Identify areas of non-compliance and implement corrective and preventive actions (CAPAs).
• Mentor and support QA and Production team members to build a culture of collaboration, continuous improvement, and compliance excellence.
• Perform other QA-related tasks as assigned, in support of overall quality objectives.
  
  

Qualifications & Requirements:

• Minimum of 10 years of Quality Assurance experience, with a strong focus on cGMP compliance in the OTC and/or cosmetic industry.
• Proven track record of designing and implementing effective QA/QC compliance programs.
• Hands-on experience with authoring and reviewing validation protocols and reports, as well as other GMP documentation.
• Strong understanding of regulatory expectations, including FDA guidelines and relevant industry standards.
• Excellent communication, problem-solving, and organizational skills.
  
  

This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

INDBH

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Part-time

Job function

• Job function

  Quality Assurance

• Industries

  IT Services and IT Consulting

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