Associate Director Quality Assurance
: Job Details :


Associate Director Quality Assurance

Arevna

Location: San Antonio,TX, USA

Date: 2025-01-01T18:08:39Z

Job Description:

Job Title: Senior Quality Manager / Associate Director

Industry: Generics Pharmaceutical Manufacturing

About the Company:

Arevna is partnering with a fast-growing biopharmaceutical company based in Texas. This innovative organization is expanding its operations and is seeking a dynamic Senior Quality Manager/Associate Director to lead key quality initiatives and ensure compliance in a regulated generics manufacturing environment.

Key Requirement:

Candidates must have hands-on experience in generics development and a strong understanding of Chemistry, Manufacturing, and Controls (CMC).

Role Overview:

In this critical role, you will manage the quality assurance systems and processes, ensuring compliance with FDA regulations and GMP standards. You will play a significant role in the preparation and management of ANDA submissions and provide strategic guidance on quality issues.

Key Responsibilities:

  • Develop, implement, and maintain quality systems, including CAPA, change control, deviation management, and audit programs.
  • Lead or support the preparation of ANDA filings, ensuring compliance with CMC requirements.
  • Collaborate with regulatory, manufacturing, and R&D teams to address quality-related aspects of generics development.
  • Support internal and external audits, ensuring readiness for FDA and other regulatory inspections.
  • Oversee supplier and vendor qualification processes to ensure compliance with quality standards.
  • Conduct risk assessments and contribute to continuous improvement initiatives in quality systems.
  • Train and mentor team members on quality practices and regulatory compliance.

Qualifications:

  • Bachelor's degree in a scientific or technical discipline; advanced degree preferred.
  • 5+ years of quality assurance experience in a regulated pharmaceutical environment, with a focus on generics manufacturing.
  • Strong knowledge of FDA regulations, GMP standards, and CMC processes.
  • Proven experience supporting ANDA submissions.
  • Excellent problem-solving skills, with a demonstrated ability to lead root cause analysis and implement effective CAPAs.
  • Strong interpersonal and communication skills with the ability to work collaboratively across teams.

Compensation:

Competitive salary package, with opportunities for professional growth and development.

Apply Now!

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