Document Controller

Document Controller

Montrose Temporary No home office possible
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At a Glance

  • Tasks: Manage the Veeva Quality Docs system and support users in document management.
  • Company: Join a global pharmaceutical leader dedicated to improving health worldwide.
  • Benefits: Earn between Β£18 to Β£20/hour with a supportive work environment.
  • Why this job: Make a real difference in healthcare while developing valuable skills.
  • Qualifications: SVQ Level 3 or equivalent required; training provided.
  • Other info: Temporary role for 9 months with opportunities for growth.

Overview

Document Controller
On site Montrose, Scotland
Shift: Monday to Friday
8am – 4:30pm
From Β£18 to Β£20/hour

Our respected client, a global pharmaceutical company manufacturing a diverse range of products including medically sterile products, equipment and medicines that help to save the lives of millions of people worldwide. GSK are committed to moving Ahead Together and aim to have a positive impact on the health of 2.5 Billion people by the end of 2030. We are looking for candidates to join our team of exceptional individuals doing work that truly matters to the health of people worldwide.

The successful candidate will provide management of the Veeva Quality Docs (VQD) system, the core GxP Documentation System on site.

Responsibilities

  • Provide role of VQD Process owner, including acting as superuser and local business administrator (LBA), as well as Release-coordinator for Montrose entity.
  • Provide training and coaching to users on how to use VQD effectively and efficiently.
  • Provide site-wide support and guidance to users on how to create, edit, review, approve, and retire documents in VQD.
  • Troubleshoot and resolve any issues or difficulties that users may encounter in using VQD, such as selecting the appropriate document type, subtype, and classification, completing the required metadata fields, cancelling checkouts, initiating and completing workflows, reassigning tasks, cancelling workflows, adding associations and relationships, sharing views, managing periodic reviews and retention periods, and deleting documents after the end of their retention period.
  • Responsible for controlled printing at site including issuing, performance and how and when to use the controlled print function.
  • Maintenance and lifecycle management of VQD documentation including metadata accuracy, document change requests, movers/leavers access, periodic reviews and access reviews.
  • Performance management of VQD documentation through monitoring and reporting against key documentation KPIs.
  • Work closely with L&D to ensure alignment for mylearning and LSOP management.
  • Participate in wider VQD forums.
  • Act as point of contact for the Archives facility (Archives Champion for documentation queries), including preservation notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries.

Qualifications

  • SVQ Level 3: Higherers / higher national certificate / apprenticeship or equivalent.

This role is recruited on a temporary basis for a 9 months duration.

Why GSK?

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it\’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We\\\’re committed to ensuring that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. GSK is open to all talent and is an Equal Opportunity Employer. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class (US only).

Should you require any support or assistance on your application, please contact your local Gi Group office directly.

Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Gold status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.

Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role.

We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.

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Document Controller employer: GI Group Main Account

GSK is an exceptional employer located in Montrose, Scotland, dedicated to making a positive impact on global health. With a strong commitment to employee growth and inclusivity, GSK fosters a supportive work culture where individuals can thrive while contributing to meaningful projects that save lives. The company offers competitive pay, comprehensive training, and opportunities for professional development, making it an attractive place for those seeking rewarding employment in the pharmaceutical industry.
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Contact Detail:

GI Group Main Account Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Document Controller

✨Tip Number 1

Network like a pro! Reach out to people in the industry, especially those already working at GSK. A friendly chat can sometimes lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for the interview by researching GSK's values and recent projects. Show them you’re not just another candidate; you’re genuinely interested in their mission to impact global health.

✨Tip Number 3

Practice common interview questions related to document control and quality management. We want you to feel confident discussing your experience with systems like Veeva Quality Docs.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the GSK team.

We think you need these skills to ace Document Controller

Veeva Quality Docs (VQD) Management
Document Control
Training and Coaching
Troubleshooting
Metadata Management
Performance Management
Key Performance Indicators (KPIs) Monitoring
Collaboration with Learning and Development (L&D)
Archiving and Documentation Queries
Controlled Printing Management
Workflow Management
Attention to Detail
Communication Skills
Problem-Solving Skills

Some tips for your application 🫑

Tailor Your CV: Make sure your CV is tailored to the Document Controller role. Highlight relevant experience with documentation systems like Veeva Quality Docs and any training or coaching you've provided in the past.

Showcase Your Skills: Don’t forget to showcase your skills in managing documentation and troubleshooting issues. Use specific examples that demonstrate your ability to handle tasks like document approvals and metadata management.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Explain why you’re passionate about working with GSK and how your background aligns with their mission to improve global health. Keep it engaging and personal.

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way to ensure your application gets the attention it deserves, so don’t miss out!

How to prepare for a job interview at GI Group Main Account

✨Know Your Veeva Quality Docs

Familiarise yourself with the Veeva Quality Docs (VQD) system before your interview. Understand its functionalities, especially how to create, edit, and manage documents. This will show your potential employer that you're proactive and ready to hit the ground running.

✨Showcase Your Training Skills

Since the role involves training users on VQD, prepare examples of how you've successfully trained or coached others in the past. Highlight your communication skills and ability to simplify complex processes, as this is crucial for the position.

✨Be Ready to Troubleshoot

Anticipate questions about troubleshooting common issues within the VQD system. Brush up on potential problems users might face and think through solutions. This will demonstrate your problem-solving abilities and technical knowledge.

✨Understand GSK's Values

Research GSK’s mission and values, particularly their commitment to health and inclusivity. Be prepared to discuss how your personal values align with theirs. This shows that you’re not just looking for a job, but are genuinely interested in contributing to their goals.

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