Job Summary
We are seeking a detail-oriented and organized Quality Assurance Specialist to join our team. The successful candidate will be responsible for ensuring compliance with Good Manufacturing Practices (GMP) regulations and implementing quality control measures across various projects and products.
Responsibilities:
* Guarantee cGMP compliance in all activities and systems related to project and product execution.
* Implement policies, procedures, and methods to evaluate and continuously improve the quality of products and operations throughout the product lifecycle.
* Provide global supplier qualification services in support of new product introduction and existing products.
Key Areas of Focus:
* Rigorous management of all quality activities for assigned projects and/or products.
* Promotion of high-quality levels and continuous improvement culture in relevant company activities.
* Catalyst for change and improvement in performance/quality.
Requirements:
* Bachelor's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar scientific field.
* Typically 3-5 years of relevant experience in a QA GMP environment within the Pharmaceutical Industry.
* Experience of working in a GMP operational environment.
* Training and experience of GMP standards.
We Offer:
* An opportunity to work in a dynamic and growing industry.
* A chance to contribute to the development of high-quality products.
* A collaborative and supportive work environment.