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- Tasks: Ensure quality standards in a global pharmaceutical company and support audits.
- Company: Join a leading name in the pharmaceutical industry with a focus on growth.
- Benefits: Excellent benefits package, career development, and potential for contract extension.
- Why this job: Make a real impact on quality assurance in a dynamic environment.
- Qualifications: Degree in a relevant field and experience in Quality Assurance within GMP.
- Other info: Opportunity to work on improvement projects and enhance your skills.
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 Glasgow employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist in Glasgow
✨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 Quality Assurance 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 and thinking of examples from your past experience that showcase your skills.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your career goals. Use our website to find roles that excite you, and tailor your approach to each company’s culture and values.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. Plus, it keeps you fresh in their minds as they make their decision.
We think you need these skills to ace Quality Assurance Specialist in Glasgow
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 and 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 our team. Keep it engaging and personal – we love to see your personality come through!
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 and submit your materials!
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 industry's standards and can hit the ground running.
✨Prepare for Scenario Questions
Expect questions that ask you to describe how you would handle specific quality assurance scenarios. Think about past experiences where you had to raise CAPAs or conduct audits. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly and effectively.
✨Showcase Your Communication Skills
Since strong communication is key in this role, be prepared to demonstrate how you've effectively communicated with different teams in the past. Share examples of how you escalated quality issues or collaborated with auditors, as this will highlight your ability to work across various levels of an organisation.
✨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 aligns with your career goals.
