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- Tasks: Join a team ensuring quality in pharmaceutical projects across the UK and Ireland.
- Company: Work with a leading pharmaceutical manufacturer based in Camberley, England.
- Benefits: Enjoy a 6-month contract with potential for growth and valuable industry experience.
- Why this job: Be part of impactful projects that enhance healthcare quality and compliance.
- Qualifications: 1-3 years in the pharmaceutical industry with GxP knowledge required.
- Other info: Opportunity to develop project management skills in a dynamic environment.
The predicted salary is between 36000 - 60000 £ per year.
I am working with a pharmaceutical manufacturing company based out of Camberley, England who are looking for a Quality Assurance consultant to join on an initial 6 month contract.
Job Purpose: To ensure compliant and efficient execution of a quality project across the UK and Ireland organizations.
- Gap assessment of the QMS for a new entity
- Project planning to ensure effective and compliant integration of current QMS with to be QMS of the established entity
- Ownership of the project planning and execution
- Implementation of project plan to ensure effective QMS in new entity
- Creation of Quality agreements and contracts
Experience: 1-3 years experience in the pharmaceutical industry, GxP knowledge. Good level of skills in the use of computer based systems and applications.
Functional Quality Knowledge/Skills:
- Quality System Management
- Understand Regulatory Environment – Knowledge of GMDP and other regulatory requirements relevant for country organisation
- Quality Governance/Compliance – Support preparation for audits and inspections
- Project management experience for Quality
Quality Consultant employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Consultant
✨Tip Number 1
Familiarise yourself with the specific quality management systems (QMS) used in the pharmaceutical industry. Understanding how these systems operate will give you a significant edge during interviews, as you'll be able to discuss relevant experiences and insights.
✨Tip Number 2
Network with professionals in the pharmaceutical sector, especially those involved in quality assurance. Attend industry events or join online forums to connect with others who can provide insights or even refer you to opportunities at companies like the one we're hiring for.
✨Tip Number 3
Brush up on your knowledge of regulatory requirements such as GMDP. Being well-versed in these regulations will not only help you in the role but also demonstrate your commitment and expertise to potential employers.
✨Tip Number 4
Prepare to discuss your project management experience in detail. Be ready to share specific examples of how you've successfully managed quality projects in the past, as this will showcase your ability to take ownership and execute plans effectively.
We think you need these skills to ace Quality Consultant
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in the pharmaceutical industry, particularly focusing on Quality Assurance and GxP knowledge. Use specific examples that demonstrate your skills in Quality System Management and project management.
Craft a Strong Cover Message: In your cover message, express your enthusiasm for the role and briefly outline how your background aligns with the job requirements. Mention your experience with QMS and any relevant projects you've managed.
Highlight Regulatory Knowledge: Emphasise your understanding of the regulatory environment, including GMDP and other relevant regulations. This will show that you are well-prepared to support audits and inspections.
Proofread Your Application: Before submitting, carefully proofread your CV and cover message for any errors or typos. A polished application reflects your attention to detail, which is crucial in Quality Assurance roles.
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Quality Systems
Make sure you have a solid understanding of Quality Management Systems (QMS) and how they apply to the pharmaceutical industry. Be prepared to discuss your experience with QMS, including any gap assessments you've conducted or project plans you've implemented.
✨Familiarise Yourself with Regulatory Requirements
Brush up on GxP guidelines and other regulatory requirements relevant to the UK and Ireland. Showing that you understand the regulatory environment will demonstrate your capability to support audits and inspections effectively.
✨Highlight Your Project Management Skills
Since the role involves ownership of project planning and execution, be ready to share specific examples of projects you've managed. Discuss how you ensured compliance and efficiency in your previous roles, as this will be crucial for the position.
✨Prepare Questions for the Interviewers
Think of insightful questions to ask about the company's current QMS and the challenges they face. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
