Senior QA Associate – Operations

Job title:

Senior QA Associate – Operations

Company:

Life Science Recruitment

Job description

Sr. Associate – Quality – Biotechnology Operations
Our client, a global biotech company, are seeking a highly motivated and detail-oriented Biotechnology QA Sr. Associates to join our quality assurance team and ensure the highest standards of product quality and compliance.Key Responsibilities:
As a Biotechnology QA Sr. Associate, you will play a critical role in maintaining the quality and regulatory compliance of the biopharmaceutical products within the next-generation manufacturing facility. You will work closely with cross-functional teams to implement and uphold quality assurance standards, facilitate inspections and audits, and support continuous improvement initiatives.Quality Assurance Oversight:

• Develop and maintain quality assurance procedures, policies, and systems.
• Conduct routine self-inspections and monitoring assessments (time-on-the-floor) to ensure compliance with cGMP (current Good Manufacturing Practices) and other relevant regulations.
• Collaborate with production and QC teams to ensure product quality throughout the manufacturing process.
• Investigate and address deviations, non-conformities, and CAPA (Corrective and Preventive Actions) to maintain product quality.

Regulatory Compliance:

• Stay current with industry regulations, guidelines, and best practices.
• Assist in the preparation and execution of regulatory inspections and audits.
• Ensure that all products meet regulatory requirements, including documentation and reporting.

Documentation and Reporting:

• Maintain accurate and comprehensive quality records, including batch records, change control documentation, and quality reports.
• Prepare and review documentation related to product quality and compliance including GMP standard operating procedures, process flow documents as well as equipment qualification and process validation documentation.
• Perform batch disposition, including approval of drug substance batch records and associated CoA’s.

Quality Improvement Initiatives:

• Identify areas for process improvement and work collaboratively with cross-functional process teams to implement changes.
• Participate in risk assessments and quality improvement projects.

Training and Development:

• Provide training to staff on quality-related procedures and best practices.
• Stay informed about the latest developments in biotechnology and quality assurance.

Requirements:

• BSc Hons, MSc, or PhD in Pharmacy, Science, Engineering, Quality, or related discipline.
• Minimum of 5 years of experience in quality assurance within a biotechnology or pharmaceutical manufacturing environment.
• Strong knowledge of cGMP, FDA, Data Integrity, Quality Risk Management and other biopharmaceutical regulatory requirements.
• Experience with quality management systems (e.g., TrackWise, MES) is a plus.

For more information, contact Sinéad on / +353879500821

Expected salary

Location

Limerick

Job date

Fri, 29 Mar 2024 06:06:01 GMT

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