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- Tasks: Join our team to ensure quality in the pharmaceutical industry through audits and documentation.
- Company: Work with a global leader in pharmaceuticals, known for innovation and excellence.
- Benefits: Enjoy an excellent benefits package with opportunities for growth and development.
- Why this job: Make a real impact on quality assurance while collaborating with diverse teams and clients.
- Qualifications: Degree in a relevant field and several years of QA experience in a GMP environment required.
- Other info: Be part of improvement projects and gain exposure to regulatory audits.
The predicted salary is between 36000 - 60000 £ per year.
SRG are working with a global name in the pharmaceutical industry to help them find a QA Specialist to join their team.
If you have Quality Assurance (QA) experience from a GMP environment then this could be a great next step for you.
The company offer an excellent benefits package and scope for growth and development.
The Role:
- Perform batch reviews within required timelines
- Author and review SOPs
- Document and report all work in adherence with GMP and departmental procedures
- Review change controls and provide feedback / corrections to authors and escalate concerns to the Quality Manager/Head of Quality where necessary
- Raise, approve and review CAPAs
- Represent the QA team for improvement projects and with clients and internal teams
- Assist in the performance of supplier audits, supporting the Lead Auditor
- Acts as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and information
- Conducts self-inspections / audits to ensure compliance with Quality Management System procedures and GMP regulations
- Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management
- Carries out site internal audits and identifies areas of GMP improvement during their daily duties
- Carries out training for QMS activities as defined by line management
Requirements:
- Degree in a relevant scientific, engineering or business discipline and/or relevant industry experience
- Several years’ experience within Quality Assurance working to GMP guidelines
- Experience of working within a Quality Management System e.g. completing or reviewing QMS documentation (SOPs/Deviations /Investigations /CAPA)
- Experience of preparing and assisting in external audits with regulatory bodies such as FDA and MHRA
- Organised and attention to detail
- Strong communication skills across all levels
Quality Assurance Specialist employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist
✨Tip Number 1
Familiarize yourself with GMP guidelines and Quality Management Systems. Understanding these frameworks will not only help you in interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those working in QA roles. Engaging with them can provide insights into the company culture and expectations, which can be beneficial during your application process.
✨Tip Number 3
Prepare for potential technical questions related to SOPs, CAPAs, and audit processes. Being able to discuss your experience confidently will set you apart from other candidates.
✨Tip Number 4
Showcase your communication skills by practicing how to articulate complex QA concepts clearly. This is crucial as the role requires interaction with various teams and clients.
We think you need these skills to ace Quality Assurance Specialist
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Assurance Specialist position. Highlight key responsibilities and requirements that align with your experience, especially those related to GMP and Quality Management Systems.
Tailor Your CV: Customize your CV to emphasize your relevant QA experience, particularly in GMP environments. Include specific examples of your work with SOPs, CAPAs, and audits to demonstrate your expertise.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the role. Mention your degree, relevant experience, and how your skills can contribute to the company's goals in quality assurance.
Highlight Communication Skills: Since strong communication skills are essential for this role, provide examples in your application that showcase your ability to communicate effectively across different levels, whether in documentation or during audits.
How to prepare for a job interview at SRG
✨Showcase Your GMP Experience
Make sure to highlight your experience working in a GMP environment. Be prepared to discuss specific examples of how you've adhered to GMP guidelines and contributed to quality assurance processes.
✨Familiarize Yourself with SOPs
Since the role involves authoring and reviewing SOPs, brush up on your knowledge of standard operating procedures. Be ready to discuss your experience with SOP documentation and any improvements you've implemented in the past.
✨Prepare for Audit Scenarios
Given the importance of audits in this role, think about your experiences with internal and external audits. Prepare to share how you've supported audit teams and responded to regulatory requests, particularly with bodies like the FDA and MHRA.
✨Demonstrate Strong Communication Skills
Effective communication is key in this position. Practice articulating your thoughts clearly and confidently, especially when discussing quality issues and collaborating with different teams. Be ready to provide examples of how you've successfully communicated across various levels of an organization.
