Job Details

Director Project Engineering (gn)

Marburg, Hessen, Deutschland

CSL Behring GmbH

Jetzt bewerben
Project Management Project Management Office Green Field Engineering CAPEX OPEX Master Black Belt Lean Six Sigma Anlagentechnik Pharmaproduktion

Beschäftigungsart

Beschäftigungsverhältnis
Festanstellung
Befristung
unbefristet
Arbeitszeit
vollzeit
Home Office
nein

Beschreibung

Driven by Our Promise

With operations in more than 30 nations and over 16,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

Our Engineering Department in Marburg is looking for a Director Project Management (gn)

Main responsibilities and accountabilities:

  • Leads, motivates and develops department and direct reports in line with the company values and the Marburg leadership promise
  • Ensures education and training of department staff to maintain and further develop know-how and meet applicable cGMP standards.
  • Develops and defines strategic direction of Analytical Services Quality (ASQ).
  • Responsible for the effective management and operation of Analytical Services Quality (ASQ) Marburg. Defines objectives for the department in alignment with the objectives of the company and assures availability of adequate performance indicators for the department.
  • Ensures timely, efficient and GMP-compliant performance and documentation of all quality tests for starting materials, IPCs (in process controls), active pharmaceutical ingredients, packaging materials including medical devices, final products and manufacturing environment according to applicable quality rules to warrant product quality and safety. Assures efficient processes, data integrity and timely availability of data to all customers.
  • Assures that the Quality Control documentation and its archiving comply with cGMP and regulatory requirements and support regulatory filings (change control).
    Responsible for the continuous improvement of general processes in the department. Contributes to continuous improvement of processes and products in the company.
    Assures maintenance of legal and internal health and safety standards.
  • Responsible for the assigned products as `Leiter der Qualitätskontrolle` according to AMWHV and to internally assigned tasks (SOP 505401).
    Strong accountability for developing relationship with key stakeholders in projects as well as daily routine.
  • Strong accountability for developing relationship with key stakeholders in projects as well as daily routine.

Qualifications and experiences:

  • PhD in Natural Sciences or Pharmacy or equivalent
  • At least eight years of experience in pharmaceutical or diagnostic industry and with GxP requirements
  • Experience in building effective teams and leadership of teams of a significant size
  • Experience in Quality assessment of biological pharmaceutical products and international inspections
  • Knowledge in protein analytics, especially blood proteins
  • Knowledge of international requirements regarding  cGMP and analytical testing of medicines
  • English and German fluently in speaking and writing
  • Drives results, directs work and ensures accountability
  • Communicates effectively
  • Develops talents, drives engagement and builds effective teams
  • Optimizes work processes and cultivates Innovation
  • Manages ambiguity, situational adaptability

We look forward to receiving your application!


Jetzt bewerben