GxP Document Controller (Part-Time, Onsite) | DocuSign Expert
GxP Document Controller (Part-Time, Onsite) | DocuSign Expert

GxP Document Controller (Part-Time, Onsite) | DocuSign Expert

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

  • Tasks: Manage GxP documents and ensure compliance with regulations in a dynamic environment.
  • Company: Leading international pharmaceutical company based in Greater London.
  • Benefits: Competitive salary, annual leave, bonus scheme, and part-time flexibility.
  • Why this job: Join a reputable company and gain valuable experience in Quality Systems.
  • Qualifications: 1-2 years of experience in a Quality Systems environment required.
  • Other info: Part-time, 12-month fixed-term contract with training opportunities.

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

A leading international pharmaceutical company located in Greater London is seeking a QS Document Controller to manage GxP documents and ensure compliance with regulatory requirements. This part-time, 12-month fixed-term contract role involves overseeing document lifecycles and providing training to various departments.

The ideal candidate will have at least 1-2 years of experience in a Quality Systems environment.

The position offers competitive salary and attractive benefits, including annual leave and a bonus scheme.

GxP Document Controller (Part-Time, Onsite) | DocuSign Expert employer: Ethypharm

Join a leading international pharmaceutical company in Greater London, where you will thrive in a dynamic work culture that prioritises compliance and quality. As a GxP Document Controller, you will benefit from competitive salaries, attractive annual leave, and a bonus scheme, all while enjoying opportunities for professional growth and development in a supportive environment.
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Contact Detail:

Ethypharm Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land GxP Document Controller (Part-Time, Onsite) | DocuSign Expert

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for a GxP Document Controller 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 knowledge of GxP regulations and document control processes. We recommend practising common interview questions related to compliance and quality systems, so you can showcase your expertise confidently.

✨Tip Number 3

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

✨Tip Number 4

Apply through our website for the best chance at landing that part-time gig! We make it easy for you to showcase your skills and experience directly to the hiring team, increasing your chances of getting noticed.

We think you need these skills to ace GxP Document Controller (Part-Time, Onsite) | DocuSign Expert

GxP Document Management
Regulatory Compliance
Quality Systems Knowledge
Document Lifecycle Management
Training and Development
Attention to Detail
Communication Skills
Organisational Skills
Problem-Solving Skills
Experience in Pharmaceutical Industry

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in managing GxP documents and compliance. We want to see how your skills match the role, so don’t be shy about showcasing relevant projects or achievements!

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 QS Document Controller role. We love seeing enthusiasm and a clear understanding of the job requirements.

Showcase Your Training Skills: Since this role involves providing training, mention any experience you have in this area. We’re looking for someone who can effectively communicate and share knowledge with different departments.

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 during the process!

How to prepare for a job interview at Ethypharm

✨Know Your GxP Inside Out

Make sure you brush up on Good Practice (GxP) guidelines before the interview. Familiarise yourself with the specific regulations relevant to the pharmaceutical industry, as this will show your potential employer that you’re serious about compliance and understand the importance of document control.

✨Showcase Your DocuSign Skills

Since the role requires expertise in DocuSign, be prepared to discuss your experience with this tool. Bring examples of how you've used it to streamline document processes or improve compliance in previous roles. This will demonstrate your practical knowledge and ability to contribute from day one.

✨Prepare for Scenario Questions

Expect questions that assess your problem-solving skills in a Quality Systems environment. Think of specific scenarios where you had to manage document lifecycles or train colleagues. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly and effectively.

✨Highlight Your Training Experience

Since part of the job involves providing training to various departments, be ready to discuss any previous training experiences. Share how you’ve successfully communicated complex information to different audiences, as this will showcase your ability to engage and educate others in a professional setting.

GxP Document Controller (Part-Time, Onsite) | DocuSign Expert
Ethypharm
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  • GxP Document Controller (Part-Time, Onsite) | DocuSign Expert

    Part-Time
    36000 - 60000 Β£ / year (est.)
  • E

    Ethypharm

    50-100
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