Documentation Controller

Elanco; Liverpool; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player is seeking a Documentation Controller to oversee GMP documentation management. In this role, you will ensure compliance with quality standards and support document creation and training processes. Join a diverse and innovative team that values creativity and fosters professional growth. This position offers the chance to make a real impact in the animal health sector while developing your skills in a supportive environment. If you are detail-oriented and passionate about documentation management, this opportunity is perfect for you.

Qualifications

• Proficient in Microsoft Office Suite.
• Experience with document management systems.

Responsibilities

• Manage GMP documentation and ensure compliance.
• Support document creation and revision processes.

Skills

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Veeva Quality Doc

SuccessFactors

Tools

Electronic Document Management System (EDMS)

Job description

Elanco Liverpool, England, United Kingdom

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Elanco Liverpool, England, United Kingdom

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At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose – to advance the health of animals, people, the planet and our enterprise.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Position Description:

• Management of GMP / controlled documentation across the Site to ensure that it remains up to date and in compliance with all relevant procedures.
• Act as the initial point source for any questions and/or support required relating to document creation/revision, training administration and Learning Plan management.
• Controlled printing and issuing of manufacturing documentation, including Batch Production Records Laboratory Workbooks and Production Logbooks to site.
• Provide business support to the areas assuring compliance with relevant Quality and EHS standards. Ensure business continuity.
  
  

Your Responsibilities:

Manage documents through the document management process. Activities include:

• Issuing documents according to periodic review schedule.
• Revising documents as and when requested by document owners or authors.
• Providing support to authors, assisting with formatting of documents, completion of forms such as Controlled Document Change Request Form.
• Track documents throughout the change process, liaising with authors to ensure target due dates for review and approval are met.
• Enforce rules between approval and effective dates for documents which need to be trained out.
• Make effective documents available to teams and (if required) controlled paper copies ready for collection and signing for.
  
  

Prioritising and supporting team and individual learning plans

• Conduct L&D induction for transfers and new starters to provide orientation around use of E-Learning system, re-prioritisation of Learning Plans, how to book instructor led training courses and working with Supervisors to ensure employees meet the 100% compliance.
• Maintain Learning plans by processing training records
• Assist Supervision with training metrics reports (as requested or agreed with local leadership) bringing any specific items of concern to their attention.
  
  

Systems/Process Support to team

• Use of electronic document management system (EDMS) for controlling documents and electronic quality management system for training record updates.
• Basic troubleshooting within EDMS.
• Assist document owners and authors to enable understanding of the process for creation/revision of controlled documents and associated training.
  
  

Filing and archiving of documents.

• Maintain paper files for documents as required, ensuring all appropriate documentation are filed appropriately.
• Assist in the maintenance of site archive as required in accordance with local SOP and provide support for document retrieval during audits
  
  

Printing of Batch Production Records and Laboratory Workbooks for the site. This activity will encompass the following tasks

• Ascertain the weekly demand for these documents
• Print check and bind the documents as required
• Log and issue documents to the appropriate departments
  
  

Control the issuing and retrieval of logbooks

• Maintain the Batch Production Record printing and archiving processes in a state of compliance
• Propose actions to rectify any issues raised work on their implementation
  
  

Continuous Improvement

• Assist in improvement activities to the document management and training process.
  
  

Embrace new technologies / systems designed to improve the document management and training process.

What You Need to Succeed (minimum qualifications):

• Proficient in Microsoft Word, Excel and PowerPoint
• Experience in using Veeva Quality Doc and SuccessFactors
  
  

What will give you a competitive edge (preferred qualifications):

• Experience of cGMP within Pharmaceutical manufacturing site or other regulated industry.
  
  

Additional Information:

• Location: Speke, UK
  
  

Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Accounting/Auditing and Finance

• Industries

  Pharmaceutical Manufacturing

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