Hybrid Process Quality Manager - Pharma Compliance & Audits in Slough
Hybrid Process Quality Manager - Pharma Compliance & Audits

Hybrid Process Quality Manager - Pharma Compliance & Audits in Slough

Slough Full-Time 36000 - 60000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Develop compliance policies and support clinical quality systems in a dynamic pharmaceutical environment.
  • Company: Leading global pharmaceutical company based in Slough with a strong commitment to quality.
  • Benefits: Flexible working arrangement, competitive salary, and opportunities for professional growth.
  • Why this job: Join a team that ensures quality and compliance in life-changing pharmaceutical projects.
  • Qualifications: Relevant degree and extensive experience in quality assurance within the pharmaceutical industry.
  • Other info: Work 2 days onsite and 3 days remote for a balanced work-life experience.

The predicted salary is between 36000 - 60000 Β£ per year.

A leading global pharmaceutical company in Slough is seeking a Process Quality Manager for a contract role. The successful candidate will assist in developing compliance policies, support clinical quality systems, and ensure quality risks are mitigated.

Applicants should have a relevant degree and extensive experience in quality assurance within a pharmaceutical setting, including knowledge of GCP and SOP writing.

The role offers a flexible working arrangement of 2 days onsite and 3 days remote.

Hybrid Process Quality Manager - Pharma Compliance & Audits in Slough employer: CK Group- Science, Clinical and Technical

As a leading global pharmaceutical company based in Slough, we pride ourselves on fostering a dynamic work culture that prioritises employee well-being and professional growth. Our flexible working arrangements allow for a healthy work-life balance, while our commitment to compliance and quality assurance provides meaningful opportunities for career advancement in the ever-evolving pharmaceutical industry.
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Contact Detail:

CK Group- Science, Clinical and Technical Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Hybrid Process Quality Manager - Pharma Compliance & Audits in Slough

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who have experience in quality assurance. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on GCP and SOP writing. We recommend creating a cheat sheet of key concepts and examples from your past experiences that showcase your skills in these areas.

✨Tip Number 3

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

✨Tip Number 4

Apply through our website for the best chance at landing that role! We make it easy for you to showcase your qualifications and connect directly with hiring managers.

We think you need these skills to ace Hybrid Process Quality Manager - Pharma Compliance & Audits in Slough

Quality Assurance
Compliance Policies Development
Clinical Quality Systems
Risk Mitigation
Good Clinical Practice (GCP)
Standard Operating Procedure (SOP) Writing
Pharmaceutical Industry Knowledge
Analytical Skills
Attention to Detail
Project Management
Communication Skills
Problem-Solving Skills

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in quality assurance, especially in the pharmaceutical sector. We want to see how your skills align with the role, so don’t be shy about showcasing your knowledge of GCP and SOP writing!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Process Quality Manager role. We love seeing enthusiasm and a clear understanding of compliance policies and clinical quality systems.

Showcase Relevant Experience: When filling out your application, make sure to detail your relevant experience. We’re looking for candidates who can demonstrate their ability to mitigate quality risks and support audits effectively. Be specific about your past roles!

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 this exciting opportunity. Plus, it’s super easy!

How to prepare for a job interview at CK Group- Science, Clinical and Technical

✨Know Your Compliance Policies

Make sure you brush up on the latest compliance policies relevant to the pharmaceutical industry. Being able to discuss these confidently will show that you're not just familiar with the basics, but that you’re proactive about staying updated.

✨Demonstrate Your Quality Assurance Experience

Prepare specific examples from your past roles where you've successfully managed quality assurance processes. Highlight your experience with GCP and SOP writing, as this will be crucial for the role.

✨Showcase Your Problem-Solving Skills

Think of instances where you've identified quality risks and how you mitigated them. Be ready to discuss your thought process and the outcomes, as this will demonstrate your analytical skills and ability to handle challenges.

✨Ask Insightful Questions

Prepare thoughtful questions about the company’s current quality systems and future goals. This shows your genuine interest in the role and helps you assess if the company aligns with your career aspirations.

Hybrid Process Quality Manager - Pharma Compliance & Audits in Slough
CK Group- Science, Clinical and Technical
Location: Slough
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