Associate Director Quality Assurance Job at Arevna, San Antonio, TX

YVYyZy9iS3d2Q0RPZ3p2VVYvdTQ3djQ9
  • Arevna
  • San Antonio, TX

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.

Job Tags

Similar Jobs

The AES Corporation

Legal Counsel Job at The AES Corporation

 ...committed to meeting the Paris Agreements goals by 2050. Legal Counsel Clean Energy Provide advice and counsel to...  ...relevant legal experience, preferably at a major law firm or in?house. R enewable energy experience; wind energy, battery storage or... 

Metropolitan Market

Meat/Seafood Assistant Team Leader Job at Metropolitan Market

 ...THE ROLE As a key member of the Meat/Seafood department leadership team, the Meat/Seafood Assistant Team Leader has a breadth of responsibilities spanning from team member development and sales generation, to product management and merchandising. In this role, you... 

Novant Health

Registered Nurse, Pelvic Specialty Job at Novant Health

What We Offer: The Registered Nurse serves as a leader of the healthcare team at Novant Health by establishing an authentic personalized...  ...nursing required. If your RN nursing license has been inactive, retired or lapsed for five years or more and you have not been licensed...