Quality Assurance
Aclinix Research is your trusted partner for sourcing top-tier talent in Quality Assurance (QA) and Quality Control (QC) within the life sciences sector. Our expertise extends across a comprehensive spectrum of quality management areas, enabling us to assist organizations in meeting stringent regulatory requirements and maintaining the highest standards of quality across their operations.
With our support, life sciences companies gain access to skilled professionals who specialize in ensuring compliance with a range of regulatory frameworks, including Good Laboratory Practices (GLP), Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GVP), and Good Manufacturing Practices (GMP). Whether you’re conducting preclinical studies, clinical trials, or post-market surveillance, we have the talent to bolster your quality management efforts at every stage of the research and development lifecycle.
Our network includes QA and QC experts with in-depth knowledge of industry best practices, regulatory guidelines, and quality standards. These professionals play a pivotal role in implementing robust quality systems, conducting audits and inspections, managing deviations and CAPAs (Corrective and Preventive Actions), and ensuring the integrity and reliability of data and processes.
By partnering with Aclinix Research, organizations gain a competitive edge in maintaining product quality, safeguarding patient safety, and achieving regulatory compliance. We understand the critical importance of quality management in the life sciences sector, and we’re committed to helping our clients build and sustain excellence in every aspect of their operations.
Here's a glimpse of the searches we've supported
Oversees the development and implementation of quality management systems, policies, and procedures to ensure compliance with regulatory requirements and industry standards.
Performs analytical testing and inspections on raw materials, in-process samples, and finished products to assess quality and compliance with specifications.
Designs and executes validation protocols for equipment, processes, and systems to ensure they meet regulatory requirements and perform as intended.
1.Monitors regulatory changes, assesses their impact on operations, and develops strategies to maintain compliance with applicable regulations and standards.
Conducts internal and external audits to evaluate compliance with quality management systems, procedures, and regulations, and identifies areas for improvement.
Manages the creation, review, and maintenance of quality-related documents, including standard operating procedures (SOPs), batch records, and regulatory submissions.
Ensures compliance with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), or Good Clinical Practices (GCP) through training programs, inspections, and audits.
Coordinates the identification, investigation, and resolution of deviations, non-conformances, and complaints to prevent recurrence and improve processes.
Evaluates and qualifies suppliers and vendors to ensure they meet quality and regulatory requirements for raw materials, components, and services
1.Manages and maintains quality management systems, such as document control, change control, and training programs, to ensure compliance and efficiency.
Our team is adept at sourcing top-tier talent across the following functional domains:
- Implementation of Quality Management Systems (QMS)
- Audit Preparation and Execution
- Validation and Qualification Activities
- CAPA (Corrective and Preventive Actions) Management
- Quality Risk Management
- SOP (Standard Operating Procedure) Development and Revision
- Training and Development Programs
- Continuous Improvement Initiatives