Quality Consulting Group, LLC

JT371- SPECIALIST QA

Quality Consulting Group, LLC  •  Juncos, PR (Onsite)  •  4 hours ago
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Job Description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

  • Perform quality disposition decisions (approval/rejection) for bulk drug substances in compliance with regulatory standards.
  • Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), and other applicable regulations.
  • Ensure all deviations are properly identified, investigated, documented, and resolved according to procedures.
  • Ensure that changes that could potentially impact drug substance quality are assessed according to procedures
  • Verify that production records and laboratory results are complete, accurate, and compliant with established procedures.
  • Ensure facilities, equipment, materials, and processes meet regulatory and quality requirements.
  • Lead and support continuous improvement initiatives, driving operational efficiency and quality enhancements.
  • Collaborate cross-functionally to ensure Quality Management System (QMS) processes are properly executed.
  • Support and participate in internal and external audits and regulatory inspections, serving as a Quality representative when needed.
  • Provide quality oversight and support for New Product Introduction (NPI) activities.


Qualifications:

  • Bachelor’s degree in Life Sciences or Engineering
  • 4 + years of directly related QA experience in a regulated manufacturing environment
  • Experience performing batch record (EBR) review, approval, and reconciliation
  • Experience as Manage events and decision making
  • Oversight manufacturing operations (during a 12-hour night shift (5:00 PM – 5:30 AM), providing rotating coverage that includes weekends and holidays.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

Quality Consulting Group, LLC

About Quality Consulting Group, LLC

The Quality Consulting Group is a pharmaceutical, biotechnology, food and medical device specialty consultant that supports the manufacturing industry; services are provided in multiple areas including: Regulatory Compliance, Quality Operations, Validation, Manufacturing, Training and Technical Support. Starting, as individual services provider since 2002, Quality Consulting Group has supported clients implementing the latest standards such as Validation Guidance, ICH Guidelines, and Process Excellence and Risk Management tools.

Quality Consulting Group has provided expertise in such areas as: business, operational, quality, regulatory and manufacturing strategies; organizational structures; management controls; manufacturing and quality systems methodologies and practices; compliance programs; and accuracy reviews; FDA, EMEA and other regulatory matters.

Industry
Consulting & Advisory
Company Size
11-50 employees
Headquarters
San Juan, PR
Year Founded
2011
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