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- Tasks: Ensure quality standards in pharmaceutical products and support audits.
- Company: Global leader in the pharmaceutical industry with a focus on quality.
- Benefits: Excellent benefits package, growth opportunities, and potential for contract extension.
- Why this job: Join a dynamic team and make a real impact on product quality.
- Qualifications: Degree in a relevant field and experience in Quality Assurance.
- Other info: Collaborative environment with opportunities for professional development.
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 offers an excellent benefits package and scope for growth and development. This role is for an initial 12 months with a strong likelihood of being extended from there.
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
- Act as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and information
- Conduct self-inspections / audits to ensure compliance with Quality Management System procedures and GMP regulations
- Ensure timely and effective communication and escalation of quality issues to the appropriate levels of management
- Carry out site internal audits and identify areas of GMP improvement during daily duties
- Carry 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 in Milton employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist in Milton
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the hunt for a QA Specialist role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and QA processes. We recommend practising common interview questions related to Quality Assurance, so you can confidently showcase your experience and skills when it counts.
✨Tip Number 3
Don’t forget to highlight your achievements! When discussing your past roles, focus on specific examples where you improved processes or contributed to successful audits. This will help you stand out as a candidate who can add real value.
✨Tip Number 4
Apply through our website! We make it super easy for you to find and apply for QA Specialist roles. Plus, it shows you're serious about joining our team and helps us keep track of your application.
We think you need these skills to ace Quality Assurance Specialist in Milton
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your Quality Assurance experience, especially in GMP environments. We want to see how your skills match the job description, so don’t be shy about showcasing relevant projects or achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about QA and how your background makes you a perfect fit for this role. We love seeing enthusiasm and a personal touch!
Showcase Your Attention to Detail: In QA, attention to detail is key. When filling out your application, double-check for any typos or errors. We appreciate candidates who take the time to ensure their application is polished and professional.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts!
How to prepare for a job interview at SRG
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss how you've applied these principles in your previous roles, especially when it comes to batch reviews and SOPs. This will show that you understand the importance of compliance in the pharmaceutical industry.
✨Prepare for Technical Questions
Expect questions about Quality Management Systems and your experience with CAPAs, deviations, and audits. Think of specific examples from your past work where you successfully navigated these processes. This will demonstrate your hands-on experience and problem-solving skills.
✨Showcase Your Communication Skills
Since this role requires strong communication across all levels, be prepared to discuss how you've effectively communicated quality issues or improvements in the past. Use examples that highlight your ability to escalate concerns appropriately and collaborate with teams.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the company’s approach to continuous improvement or how they handle supplier audits. This shows your genuine interest in the role and helps you gauge if the company is the right fit for you.
