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Quality Project Specialist
- Location: Hybrid (Camberley)
- Contract: 6-Month Fixed Term
- Pay Rate: 27.63 - 31.77 per hour
Job Purpose:
To ensure the compliant and efficient execution of a quality project across the UK and Ireland organisations, including gap assessment, project planning, and implementation of a Quality Management System (QMS) for a new entity.
Key Responsibilities:
* Conduct a gap assessment of the current QMS for a newly established entity.
* Lead the planning and execution of the project to integrate the existing QMS with the new entity's QMS.
* Drive the implementation of the project plan to ensure an effective and compliant QMS.
* Create and manage Quality Agreements and Contracts.
* Execute quality management system elements to support GMDP activities.
* Assess SOPs, documents, records, and metrics related to QMS systems and identify areas for improvement.
* Support audits, inspections, and self-inspection programmes as required.
* Ensure compliance by following SOPs and using IT systems effectively.
* Maintain awareness of IT platforms/applications relevant to quality processes.
* Ensure timely completion of individual and team-related quality actions and training.
Education & Qualifications:
* Degree in Life Sciences or related field.
Experience & Skills:
* 1-3 years of experience in the pharmaceutical industry with knowledge of GxP regulations.
* Proficiency in computer-based systems and applications.
* Strong organizational and multitasking skills, with the ability to manage multiple priorities.
* Ability to challenge inefficient processes and suggest improvements.
* Resilience, self-motivation, and a results-oriented approach.
Desirable Knowledge & Skills:
* Understanding of GMDP regulations and their impact on country operations.
* Experience in Quality System Management and compliance frameworks.
* Ability to support audit and inspection preparation.
* Project management experience within a Quality function.
This is a hybrid role with no fixed office days, offering flexibility for candidates based in the UK. If you have a passion for quality and regulatory compliance in the pharmaceutical industry, we encourage you to apply!
Please be aware this advert will remain open until the vacancy has been filled. Interviews will take place throughout this period, therefore we encourage you to apply early to avoid disappointment.
Tate is acting as an Employment Business in relation to this vacancy.
Tate is committed to promoting equal opportunities. To ensure that every candidate has the best experience with us, we encourage you to let us know if there are any adjustments we can make during the application or interview process. Your comfort and accessibility are our priority, and we are here to support you every step of the way. Additionally, we value and respect your individuality, and we invite you to share your preferred pronouns in your application.
