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- Tasks: Join a team to ensure quality compliance in pharmaceutical projects across the UK and Ireland.
- Company: Work with a leading pharmaceutical manufacturing company based in Camberley, England.
- Benefits: Initial 6-month contract with potential for growth and valuable industry experience.
- Why this job: Be part of impactful projects that shape quality systems in the pharmaceutical sector.
- Qualifications: 1-3 years in the pharmaceutical industry with GxP knowledge and project management skills.
- Other info: Opportunity to create quality agreements and contracts while enhancing your professional network.
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
If you are interested please apply or send me a message
Quality Assurance Consultant employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Consultant
✨Tip Number 1
Make sure to familiarize yourself with the specific regulatory requirements relevant to the UK and Ireland, especially GMDP. This knowledge will not only help you in interviews but also demonstrate your commitment to understanding the compliance landscape.
✨Tip Number 2
Highlight any experience you have with project management in quality assurance. Be prepared to discuss specific projects you've worked on, focusing on how you ensured compliance and efficiency throughout the process.
✨Tip Number 3
Network with professionals in the pharmaceutical industry, especially those who have experience in quality systems management. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 4
Stay updated on the latest trends and technologies in quality assurance within the pharmaceutical sector. Being knowledgeable about current tools and systems can set you apart from other candidates.
We think you need these skills to ace Quality Assurance Consultant
Some tips for your application 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Quality Assurance Consultant in the pharmaceutical industry. Familiarize yourself with the specific requirements mentioned in the job description, such as QMS integration and project management.
Highlight Relevant Experience: In your application, emphasize your 1-3 years of experience in the pharmaceutical industry. Be specific about your GxP knowledge and any relevant projects you've managed, particularly those involving quality systems.
Showcase Your Skills: Detail your skills in using computer-based systems and applications. Mention any specific tools or software you are proficient in that relate to quality assurance and project management.
Tailor Your Application: Customize your CV and cover letter to reflect the key points from the job description. Use similar language and terminology to demonstrate that you are a good fit for the role and understand the regulatory environment.
How to prepare for a job interview at Cpl Life Sciences
✨Show Your GxP Knowledge
Make sure to highlight your understanding of Good Practice (GxP) guidelines during the interview. Be prepared to discuss how you've applied these principles in your previous roles, especially in the pharmaceutical industry.
✨Demonstrate Project Management Skills
Since project planning and execution are key aspects of this role, come ready to share specific examples of projects you've managed. Discuss how you ensured compliance and efficiency in those projects.
✨Familiarize Yourself with Quality Systems
Understand the Quality Management System (QMS) and be ready to talk about your experience with it. Discuss any gap assessments you've conducted or how you've integrated different QMS in past roles.
✨Prepare for Regulatory Questions
Expect questions related to regulatory environments, such as GMDP. Brush up on relevant regulations and be prepared to explain how you've supported audit preparations and inspections in your previous positions.
