Lead Document Controller
- Denmark
- Contract
- Life Sciences
This vacancy has now expired
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Lead Document Controller to join them on their new expansion project. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
Responsibilities:
- Responsible for leading and coordinating document control processes within the project and the various phases (Engineering documents).
- Manage the engineering registry in different systems to allow accurate and easy retrieval of information for the project engineering team, ability to locate information in a timely manner and accurately is a key function of the role
- Reproduction of information into both printed and electronic format for communication to the engineering team
- Manage and coordinate with Engineering providers and Construction management partners.
- Administer List of deliverables from the engineering provider
- Create and maintain document system overview
- Document Control Management for engineering deliverables
- Coordination with CQV documents and approvals
- Maintenance of project systems, i.e. transmittals, vendor docs.
- Develops new approaches to improve or replace existing procedures or systems
Requirements:
- Experience with document management processes in large capital projects
- Experience within administration function, supporting and coordinating within large organisations/teams
- Experience in the use of Microsoft Office programs and other relevant software programs
- Fluency in English both writing and speaking
- Preferably a degree in business administration, library management or record management
If this role is of interest to you, please apply now!
I have always received a highly professional & personable service from the team at Quanta. 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 Quanta for seven years now and have always received a professional service. Quanta’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 Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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Megan
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