Project Document Controller & Assistant
- England, London
- Contract
- Life Sciences
Do you want to be involved with exciting pharmaceutical projects?
When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Project Document Controller & Assistant.
Essential Duties and Responsibilities for this role include, but are not limited to, the following:
- Act as the primary administrator and point of contact for the project document control platform (e.g., Aconex, Asite, PIMS, SharePoint, or equivalent).
- Maintain and update the document management system, ensuring proper version control, metadata tagging, and audit readiness.
- Coordinate document workflows: issue, review, approval, and distribution; working to design new processes for optimise efficiency.
- Ensure all project documentation is accurately filed and organised in accordance with internal procedures and industry standards. Assist internal and external stakeholders to ensure complete and up-to-date documentation submission.
- Provide support during audits and project reviews by retrieving or compiling documentation.
- Manage submission milestones, manage RFI logs and approval chains to ensure relevant personnel are notified appropriately to aid timely completion.
- Onboard new Project team members; train and support to use documentation management systems, document submission and review protocols. Develop guides and training resources on key functions and processes utilised by the Project.
- Monitor and ensure appropriate access permissions for Project Team members.
- Help the Main Contractor to manage the systems list, RFI log, punches.
- Support Project managers in updating the Project Execution Plan and in developing a turnover & commissioning plan.
- Proven experience in a similar role in a project environment, ideally within engineering, construction, or pharmaceutical industries.
- Strong working knowledge of document control systems (e.g., Aconex, Viewpoint, SharePoint, PIMS or similar platforms).
- Excellent organisational skills with high attention to detail and accuracy.
- Strong verbal and written communication skills in English.
- Proficiency with Microsoft Office Suite (Excel, Outlook, Word, Teams, PowerPoint).
- Ability to handle sensitive information confidentially and professionally.
- Capable of working independently and managing multiple priorities.
#LI-DH1
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
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Marcin
I manage this role.