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Beschreibung

Within the scope of parental leave replacement at the Cologne Site - Virus Clearance we have the following open position limited to 18 month


Supervisor Viral Clearance (m/f/d)

Besides your functions as GLP Study Director you will provide supervision of a team consisting of scientific and technical staff.
Support us with:Supervisor:
  • Lead and organize a small Viral Clearance team of scientists (Study Directors) and technicians (Technical Officers)
  • Oversee daily operational activities and supervise the group to ensure optimal group performance, supporting and deputizing when needed
  • Provide guidance and develop staff including performance reviews
  • Optimize and adjust study planning together with project management and other supervisors to get a detailed and structured study execution
  • Identify areas of improvements and process optimizations of work flows
  • Actively promote good communication and cooperation within the department as well as between different groups at the Charles River Cologne site
  • Report to Head of Viral Clearance
Study Director:
  • Plan, support and document GLP-complaint Viral Clearance studies in a very careful, reliable and organized way
  • Support the technical staff in the implementation of GLP-compliant Viral Clearance studies
  • Supervise and ensure the care and maintenance of the GLP system (including preparation of SOPs, assuming responsibility for devices/infrastructure, qualifying devices, validations, etc.)
  • Ensure the quality of the department’s work according to current GLP standards
  • Manage potentially infectious material, cell cultures, viruses and GMOs in accordance with the Protection Against Infection Act, the Animal Pathogens Ordinance, the Biomaterial Ordinance and the Genetic Engineering Safety Guidance
  • Communicate with domestic and foreign clients
Convince us with: This position would suit an ambitious, flexible and team-orientated individual who is motivated to achieve results and is eager to lead people. You will also be expected to have:
  • University degree in natural science, e.g. Pharmacy, (Bio-)Chemistry, Biology, Biotechnology
  • A minimum of two years as a scientist, preferably within a service company in a biotech sector, CMO or CRO
  • A minimum of two years as a team lead is preferred
  • Knowledge of the quality assurance standards, preferably GLP
  • Expertise (theoretical/practical) in the fields of cell biology, virology, microbiology
  • First experience with chromatography and Aekta systems is preferred
  • Good ability to build trustful and open working relationships in all layers of a (matrix) organization
  • Very good communication and presentation skills as well as the ability to effectively communicate with various target groups
  • Experience in leading and motivating people.
  • Strong organizational skills and ability to drive operations in a fast-changing environment
  • Fluency in both English and German (oral and written)
  • Demonstrated computer knowledge (e.g. MS Office)
We offer you:
  • a position with varied, demanding activities in a future-oriented company
  • intensive training
  • flexible working hours and adequate remuneration
  • active participation in your field of activity in a motivated team
Erstellt am: 20.02.2022 | Gültig bis: 06.03.2022

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Charles River Laboratories Germany GmbH

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