The QA Associate assists ComTrans QI Department by performing clerical tasks related to internal monitoring, incident review, research and follow up. The QA Associate assists ComTrans QI Department by performing clerical tasks related to internal monitoring, incident review, research and follow up.

Title Associate Director, Quality Assurance Pharmacovigilance Auditor (Remote) + Serve as the pharmacovigilance and quality assurance expert to review the audit language in PV suppliers’ contracts including Market Research and Patient Support Programs contracts, Business Partner Pharmacovigilance Agreements (PVAs) to ensure compliance with Takeda policies and procedures and regulatory guidance.

Assists with providing employee new hire and annual training programs including but not limited to: GMP, HACCP, Allergen, Food Defense.

Trigo’s team of dedicated Delivery Assurance Specialists, Supplier Development Specialists, Supplier Quality Engineers and Program Managers support hundreds of Customers and are deployed to thousands of Suppliers worldwide focused on achieving On-Time and On-Quality Delivery results.

TRIGO ADR Americas is the leader in the Aerospace & Defense Industry providing global Supplier Delivery Assurance, Supplier Development and Quality Management Services. As a Delivery Assurance Specialist (DAS), you will be working as a vital link between the Prime Aerospace customers and their supplier base to improve delivery performance by tracking, validating, expediting and reporting real time part delivery status.

We currently have an exciting career opportunity for an Assurance Senior Associate to join the team in our New York City, Renewable Energy office/practice. In New York City , the salary range for a Senior Assurance Associate is $85,000.00 to $140,000.00.

We are seeking a Quality Assurance Manager to support the Pilot Bio-Production Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. Serves as the Section Head of Quality Assurance at the WRAIR Pilot Bioproduction Facility (PBF.

Review and support required updates to QMS Processes, Quality System Manual (QSM), Quality Policy and Procedure Manual (QPPM), Design Quality Assurance Manual (DQAM), FAA Supplemental Quality Manuals, Repair Station Manuals (FAA, EASA, and CAAC) for compliance with internal QMS Requirements, external customer requirements, AS/ISO standards, and regulatory requirements.

5-15 years of experience in QA/QC roles within scientific research, with a demonstrated emphasis on quality assurance and compliance advancement. As the driving force behind our Quality Assurance (QA) and Quality Control (QC) efforts, you will play a critical role in ensuring that our research activities, documentation, and data uphold the highest standards of integrity, quality, and compliance with regulatory requirements.

QA/QC Manager for In Vivo Research Facility (GLP Compliance Journey) As we embark on our journey to achieve Good Laboratory Practice (GLP) compliance, we are seeking a proactive and skilled QA/QC Manager to guide us in aligning our processes with FDA regulations, including 21CFR Part 11.

Join our team as the QA/QC Manager and be an instrumental part of our transformation towards GLP compliance. Monitor emerging trends in regulatory compliance, GLP guidelines, and 21CFR Part 11 updates to drive ongoing enhancement and alignment of QA/QC practices.

Collaborate closely with cross-functional teams to develop and implement comprehensive QA/QC strategies, processes, and Standard Operating Procedures (SOPs) in line with GLP principles and FDA regulations, including 21CFR Part 11.

A unique opportunity to be a catalyst for positive change in our pursuit of GLP compliance. Familiarity with GLP principles, FDA regulations, and a keen interest in learning and implementing 21CFR Part 11 requirements.

If you are an enthusiastic QA/QC professional with a desire to shape the future of research quality and compliance, we encourage you to apply. Lead the design and implementation of a robust data integrity program, encompassing audit trails, electronic signatures, data validation, and security controls, ensuring adherence to 21CFR Part 11 guidelines.

Establish and deliver training programs that educate research staff about GLP principles, FDA regulations, and the significance of compliance, fostering a culture of awareness and accountability. Bachelor's or Master's degree in a relevant scientific field (Biology, Pharmacology, etc.