Hybrid Senior QA & Compliance Lead - GCP/GVP Audits in Slough
Hybrid Senior QA & Compliance Lead - GCP/GVP Audits

Hybrid Senior QA & Compliance Lead - GCP/GVP Audits in Slough

Slough Full-Time 48000 - 72000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead quality assurance and compliance for clinical systems in a dynamic pharmaceutical environment.
  • Company: Reputable pharmaceutical company based in Slough with a strong commitment to quality.
  • Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
  • Why this job: Make a significant impact on clinical quality and compliance in a leading organisation.
  • Qualifications: 8 years in pharmaceuticals and 2 years of SOP writing experience required.
  • Other info: Join a team dedicated to excellence and innovation in healthcare.

The predicted salary is between 48000 - 72000 Β£ per year.

A reputable pharmaceutical company in Slough is seeking a Senior Process Quality Excellence Specialist. The role involves supporting clinical quality systems, ensuring compliance with GCP and GVP standards, and leading inspection readiness activities.

Candidates must have 8 years in the pharmaceutical sector and 2 years of SOP writing experience, offering a hybrid working model with office visits twice a week.

Hybrid Senior QA & Compliance Lead - GCP/GVP Audits in Slough employer: Next-Link

Join a leading pharmaceutical company in Slough that prioritises employee well-being and professional growth. With a hybrid working model, you will enjoy flexibility while being part of a collaborative culture that values compliance and quality excellence. The company offers robust training programmes and career advancement opportunities, making it an ideal environment for those seeking meaningful and rewarding employment.
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Contact Detail:

Next-Link Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Hybrid Senior QA & Compliance Lead - GCP/GVP Audits in Slough

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical sector and let them know you're on the hunt for a Senior QA & Compliance Lead 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 GCP and GVP standards. We want you to be ready to showcase your expertise and experience in SOP writing. Practice common interview questions and think about how your past experiences align with the role's requirements.

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, shoot a quick thank-you email to express your appreciation and reiterate your interest in the position. It keeps you fresh in their minds and shows your enthusiasm.

✨Tip Number 4

Apply through our website! We make it super easy for you to submit your application for the Senior Process Quality Excellence Specialist role. Plus, it shows that you're genuinely interested in joining our team. Let's get you that dream job!

We think you need these skills to ace Hybrid Senior QA & Compliance Lead - GCP/GVP Audits in Slough

GCP Compliance
GVP Compliance
SOP Writing
Inspection Readiness
Clinical Quality Systems
Pharmaceutical Industry Experience
Quality Assurance
Process Improvement

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in the pharmaceutical sector, especially your 8 years of relevant work. We want to see how your skills align with GCP and GVP standards, so don’t hold back on those details!

Showcase Your SOP Writing Skills: Since you need 2 years of SOP writing experience, be sure to include specific examples of your work. We love seeing how you've contributed to quality systems in the past, so let us know what you've achieved!

Be Clear and Concise: When writing your application, keep it straightforward. We appreciate clarity, so avoid jargon and get straight to the point about your qualifications and why you’re a great fit for the role.

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 don’t miss out on any important updates from us during the process!

How to prepare for a job interview at Next-Link

✨Know Your GCP and GVP Standards

Make sure you brush up on Good Clinical Practice (GCP) and Good Vigilance Practice (GVP) standards. Be ready to discuss how you've applied these in your previous roles, especially in relation to compliance and quality systems.

✨Showcase Your SOP Writing Skills

Since the role requires SOP writing experience, prepare examples of SOPs you've developed. Highlight your approach to ensuring clarity and compliance, and be ready to discuss any challenges you faced during the writing process.

✨Demonstrate Inspection Readiness Experience

Think about past experiences where you led inspection readiness activities. Be prepared to share specific instances where your leadership made a difference, and how you ensured that your team was well-prepared for audits.

✨Embrace the Hybrid Model

As this position offers a hybrid working model, express your adaptability to both remote and in-office work. Share how you manage your time effectively and maintain communication with your team, regardless of where you're working from.

Hybrid Senior QA & Compliance Lead - GCP/GVP Audits in Slough
Next-Link
Location: Slough

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