Senior Quality Assurance Specialist in Slough

Senior Quality Assurance Specialist in Slough

Slough Full-Time 45000 - 55000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Support and improve Quality Management Systems in a leading pharmaceutical company.
  • Company: Join a top-tier pharmaceutical organisation in Slough with a focus on quality.
  • Benefits: Gain valuable experience in a dynamic environment with career growth opportunities.
  • Other info: Collaborate with cross-functional teams and enhance your professional skills.
  • Why this job: Make a real impact on quality assurance in the pharmaceutical industry.
  • Qualifications: Degree in Life Sciences and previous QA experience required.

The predicted salary is between 45000 - 55000 £ per year.

Our client is a leading pharmaceutical organisation looking for a Quality Specialist to join their Quality team in Slough. This is an excellent opportunity for an experienced Quality professional to take on a varied role supporting the effective operation and continuous improvement of Quality Management Systems within a GxP-regulated environment.

Key Responsibilities:

  • Support the maintenance and execution of the Quality Management System (QMS), including deviations, CAPAs, change controls and complaints.
  • Identify quality issues and risks, supporting the development and implementation of appropriate corrective actions.
  • Track quality metrics, trends and KPIs and contribute to ongoing quality improvement activities.
  • Support internal audits, self-inspections and regulatory inspection readiness.
  • Assist with supplier and vendor qualification, Quality Agreements and ongoing quality oversight.
  • Support Annual Product Quality Reviews and the maintenance of Quality training programmes and documentation.
  • Ensure GxP documentation is appropriately maintained within electronic quality and document management systems.
  • Collaborate with teams across Quality, Supply Chain, Regulatory and Pharmacovigilance to ensure GxP requirements are achieved.

The ideal candidate will have:

  • A degree in Chemistry, Biology, Pharmacy or another relevant Life Science discipline.
  • Previous Quality Assurance experience within the pharmaceutical or biopharmaceutical industry.
  • Good knowledge of GxP requirements and Quality Management Systems.
  • Experience with deviations, CAPAs and change controls.
  • Experience within a GDP environment would be highly advantageous.
  • Exposure to audits, inspection readiness, supplier quality and/or Quality Agreements would be beneficial.
  • Excellent organisational, communication and stakeholder management skills with strong attention to detail.

This is a fantastic opportunity to join a leading pharmaceutical environment in a broad Quality position, gaining exposure across multiple areas of Quality Assurance and working with a range of cross-functional teams.

Keywords:

Quality Specialist, Quality Assurance, QA Specialist, Pharmaceutical Quality, Pharma QA, Quality Management System, QMS, GxP, GMP, GDP, Good Distribution Practice, CAPA, Corrective and Preventive Action, Deviations, Change Control, Quality Systems, Quality Compliance, Audit, Self-Inspection, Inspection Readiness, Regulatory Inspection, Supplier Quality, Vendor Quality, Quality Agreements, Product Quality Review, APQR, Complaints, Document Control, eQMS, Pharmaceutical, Biopharmaceutical, Life Sciences, Slough, Berkshire, VRS9525MP.

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Senior Quality Assurance Specialist in Slough employer: VRS Recruitment

Join a leading pharmaceutical company that prioritises innovation and employee development in the heart of the bioprocessing industry. With a collaborative work culture, you will have access to cutting-edge technology and hands-on experience in upstream process development, while benefiting from opportunities for career growth and professional advancement. This role not only offers a chance to contribute to groundbreaking biologics but also fosters a supportive environment where your contributions are valued and recognised.

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Contact Details:

VRS Recruitment Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Quality Assurance Specialist in Slough

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like VRS Recruitment. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like VRS Recruitment.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like VRS Recruitment. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what VRS Recruitment is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Senior Quality Assurance Specialist in Slough

Quality Management Systems (QMS)
GxP Compliance
Deviations Management
CAPA (Corrective and Preventive Action)
Change Control
Quality Metrics Tracking
Internal Audits

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at VRS Recruitment!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show VRS Recruitment that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at VRS Recruitment!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At VRS Recruitment, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at VRS Recruitment

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at VRS Recruitment that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with VRS Recruitment’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.