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Document & Master Data Controller (m/w/d)

CAMLOG Biotechnologies GmbH

Basel
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  • Publication date:

    02 May 2022
  • Workload:

    100%
  • Contract:

    Permanent position

Document & Master Data Controller (m/w/d)

To further strengthen our team in Basel we have an
immediate opening for an

Document & Master

Data Controller (m/f/d)

Job Summary
The „Document & Master Data Controller“ joins the new Master Data team within R&D.
This position includes the unique opportunity to participate in shaping workfl ows,
templates and interfaces between R&D and the systems of the whole company. The
„Document & Master Data Controller“ is providing substantial support in setting up and
validating our document control system. After the setup, the „Document & Master Data
Controller“ remains the key user providing support to the R&D team.
Your Profi le Your Tasks
At least three years of experience Participate in setup and validation of
within a regulated environment document control system
(medical devices / pharmaceuticals) Defi ne, shape, validate and implement
At least one year of experience with ... interfaces between the business unit
Doc Control and ERP Systems and the organization (SAP / Doc-
Control)
Highly skilled user of the MS Offi ce 365
environment and know how to set up ... queries for quality relevant data for
templates. You know your way around Development and Regulatory Aff airs
MS Teams and SharePoint and ideally ... templates for our quality
know how to apply visual basic for management handbook
applications (VBA). Defi ne and take the role as key user
Experienced SAP user familiar with the for R&D data management
opportunities of the system
Basic knowledge regarding SQL Your Prospects
databases, understand relational
Opportunity to participate in the
principles, know the possibilities and
defi nition of interfaces and workfl ows
restrictions, and can execute simple
together in a highly motivated team
queries.
Ideally you are experienced in International employer with team-
computer system validation (CSV) oriented working atmosphere
according to common regulations (e.g.,
FDA 21 CFR part 820.70, FDA 21 CFR Attractive employment conditions
part 11.10, GAMP 5)
Do your professional and personal
Fluent in English and German
qualifi cations match our
Good communication skills allow you requirements? We look forward to
to acquire and ultimately implement receiving your application
stakeholder requirements from www.camlog.com/apply-online.
various functions throughout the
organization. CAMLOG Biotechnologies GmbH
Ms. Barda Abdija
Margarethenstrasse 38
CH-4053 Basel
At BioHorizons Camlog, we produce innovative jobs@camlog.com
products for implant dentistry. With our
comprehensive portfolio of implant systems and
biomaterials, we are one of the global market
leaders. We owe this position not only to
customers who value us as a reliable partner, but
also to our highly motivated teams. They ensure
the continuous development of our products and
processes as well as building long-lasting
relationships with our customers, partners, and
stakeholders.


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