At a Glance
- Tasks: Join a dynamic team to review quality records and drive improvements.
- Company: Work with a global biopharmaceutical leader in a fast-paced environment.
- Benefits: Enjoy hybrid working, hands-on experience, and career growth opportunities.
- Why this job: Perfect for ambitious QA professionals wanting to expand their skills and impact.
- Qualifications: GMP experience is essential; passion for quality assurance is a must.
- Other info: 12-month contract with potential for future opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Location: Slough, UK (Hybrid after initial period onsite)
Contract Type: 12-month contract (INSIDE IR35)
Working Hours: Monday to Friday, 37.5 hours/week
Are you ready to take the next step in your Quality Assurance career? Our client, a global biopharmaceutical leader, is looking for an Associate Principal QA Specialist to join their dynamic team in Slough. This is a fantastic opportunity for an ambitious QA professional with GMP experience to broaden their exposure in a fast-paced, science-led environment.
What’s in it for you?
- Hybrid working model – initial training onsite, then up to 2 days a week from home
- Hands-on experience supporting GMP operations and major quality systems
- Exposure to cross-functional teams in a thriving biomanufacturing environment
- Grow your career under experienced senior QA leadership
What you’ll be doing:
- Reviewing and approving quality records – deviations, CAPAs, change controls and more
- Identifying and driving continuous improvement initiatives
- Coaching business partners
Associate Principal QA Specialist - Technical Operations employer: Click To Hired
Contact Detail:
Click To Hired Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Principal QA Specialist - Technical Operations
✨Tip Number 1
Familiarise yourself with the latest GMP regulations and quality assurance practices. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, especially those working in QA roles. Attend relevant conferences or webinars to make connections that could lead to valuable insights and potential referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've driven continuous improvement initiatives in your previous roles. Highlighting your hands-on experience will set you apart from other candidates.
✨Tip Number 4
Research the company’s recent projects and achievements in the biomanufacturing sector. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show genuine interest in their operations.
We think you need these skills to ace Associate Principal QA Specialist - Technical Operations
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in Quality Assurance, particularly any GMP experience. Use keywords from the job description to demonstrate that you meet the specific requirements of the Associate Principal QA Specialist role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for Quality Assurance and your understanding of the biopharmaceutical industry. Mention specific examples of how you've contributed to quality systems or continuous improvement initiatives in previous roles.
Highlight Relevant Skills: In your application, emphasise skills that are crucial for the role, such as your ability to review and approve quality records, coach team members, and drive improvement initiatives. Be specific about your experiences that align with these responsibilities.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is essential in a QA role.
How to prepare for a job interview at Click To Hired
✨Understand GMP Regulations
Make sure you have a solid grasp of Good Manufacturing Practices (GMP) as they are crucial for the role. Be prepared to discuss how you've applied these regulations in your previous positions.
✨Showcase Your Problem-Solving Skills
Be ready to provide examples of how you've identified issues and implemented solutions in quality assurance processes. This will demonstrate your proactive approach and ability to drive continuous improvement.
✨Familiarise Yourself with Quality Systems
Research the major quality systems used in biopharmaceuticals. Being knowledgeable about these systems will help you answer questions confidently and show your commitment to the field.
✨Prepare for Behavioural Questions
Expect questions that assess your teamwork and coaching abilities. Think of specific instances where you've collaborated with cross-functional teams or mentored colleagues, as this aligns with the job's requirements.