- Implement and maintain robust quality management systems to uphold product integrity and safety.
- Collaborate closely with cross-functional teams including QC, production, and regulatory affairs to resolve quality issues and drive continuous improvement initiatives.
- Lead investigations into deviations, non-conformances, and complaints, implementing corrective and preventive actions to mitigate risks and drive process improvements.
- Provide guidance and support during internal and external audits, demonstrating a commitment to excellence and regulatory compliance.
- Demonstrated expertise in quality assurance activities, including document control, change control, CAPA management, and risk assessment.
- Excellent understanding of regulatory requirements governing the pharmaceutical industry, including FDA and MHRA guidelines.
- Strong analytical and problem-solving skills, with a keen attention to detail and a proactive approach to quality assurance.
- Exciting Challenges: Be part of a fast-paced and dynamic environment where every day brings new challenges and opportunities for growth.
- Cutting-
- Career Development: Take your career to new heights with ample opportunities for training, development, and advancement within our organization.
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QA Officer/Manager
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School Bursar
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Admissions Officer
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Admissions Officer
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Quality Assurance Officer
1 week ago
Charles River Laboratories, Research Models and Services, Germany GmbH Keele, Staffordshire, United KingdomPress Tab to Move to Skip to Content Link · Select how often (in days) to receive an alert: · At Charles River, we are passionate about improving the quality of people's lives. When you join our global family, you will help create healthier lives for millions of patients and th ...
QA Officer/Manager - Keele, Staffordshire, United Kingdom - RBW Consulting
Description
Quality Assurance Officer
Are you ready to embark on a new QA journey in the heart of the pharmaceutical industry? We're seeking a passionate and experienced Quality Assurance Officer to join a dynamic team at a state-of-the-art sterile production facility in Keele, Staffordshire.
As a QA Officer, you will play a pivotal role in ensuring the highest standards of quality and compliance are maintained throughout operations.
Conduct thorough reviews and evaluations of manufacturing processes, ensuring compliance with Good Manufacturing Practices (GMP) and regulatory standards.
Approximately 5 years of hands-on experience in GMP pharmaceutical manufacturing, with a strong background in QC, production, or QA roles.
Edge Facility:
Work in a modern, state-of-the-art facility equipped with the latest technologies and resources to support your success.
If you're ready to make your mark in the pharmaceutical industry and contribute to the advancement of healthcare, I want to hear from you Don't miss this exciting opportunity to join a dynamic team and shape the future of quality assurance in Keele, Staffordshire.
