Clinical Development Quality Officer

04.07. | Employee | 100%

Debiopharm Group™ is a Swiss-headquartered global biopharmaceutical group including five companies active in the life science areas of drug development, GMP manufacturing of proprietary drugs, diagnostic tools and investment management. Debiopharm International SA is focused on the development of prescription drugs that target unmet medical needs. The company in-licenses and develops promising drug candidates. The products are commercialized by pharmaceutical out-licensing partners to give access to the largest number of patients worldwide.

For the Quality Department, we are looking for a

Clinical Development Quality Officer

To ensure that clinical studies sponsored by Debiopharm International S.A. (DPI) and pharmacovigilance activities related to Investigational Medicinal Products (IMPs) are conducted in compliance with international guidelines (Good Clinical Practices (GCP) and applicable regulations, through the maintenance and constant improvement of adequate quality systems.

Your main responsibilities:

  • Act as GCP representative for the Clinical Development department of DPI and actively support the development of appropriate clinical development processes, systems and tools to ensure compliance with GCP;
  • Follow-up until resolution on all Corrective and Preventive action plans associated with clinical and pharmacovigilance activities resulting from any source (e.g. deviations, audits and inspections, improvement suggestions);
  • Tracking and monitoring the Quality Events (Deviations, Change Controls, CAPAs and other events) and communicating to Management the monitoring trends and related improvements in line with the applicable regulations/guidelines.
  • Promote the Quality Culture and actively collaborate to the GCP training activities through the Debiopharm Development organization;
  • Perform and coordinate the appropriate training of concerned collaborators involved in GCP activities through the oversight of the DPI training management system (Ennov Training) and the setting-up/delivery of specific training sessions on clinical quality subjects, new/revised processes, regulations/guidelines, company improvement initiatives, as needed;
  • Coordinate the external audits planning of investigational sites and Contract Research Organizations/Vendors and ensure review and follow-up or related CAPAs. Communicate to Management the CAPAs monitoring and related improvements;
  • Coordinate the internal audits planning, support the establishment of the CAPAs and ensure regular follow-up of CAPAs with the internal auditees. Communicate to Management the CAPAs monitoring and related improvements;
  • In collaboration with concerned functions, coordinate the preparation and assist in hosting external GCP audits of DPI (e.g. DPI’s partners) as well as of regulatory inspections of DPI, investigational sites, vendors and partners;
  • Maintain the Clinical Development Quality Systems and related SOPs in compliance with the laws and regulations governing GCP and the applicable guidelines for the pre-marketing pharmacovigilance (PV) activities.

Your profile:

  • University degree;
  • 2 to 5 years of experience in managing Clinical Quality Management
  • Experience in managing tracking systems such as CAPAs database resulting from GCP audits (CROs, TMF, Investigational Sites and CSR) as well as deviations, changes tracking systems;
  • Knowledge of GCP;
  • Experience in maintaining quality SOP’s;
  • Good practical experience in using validated electronic quality systems tools (TrackWise, Veeva, Ennov, etc);
  • Knowledge of computerized systems validation;
  • Rigor, flexibility, adaptability and organization;
  • Pragmatism focused on efficiency and continuous improvement;
  • Capacity to think strategically and to keep an overall view while bringing efficiency to daily detailed activities.

Debiopharm can offer you:

  • An international and highly dynamic environment of a mid-size company.
  • The opportunity to join a successful, family-owned, company, at the forefront of the most advanced scientific developments in the industry covering various therapeutic areas and modalities (small molecules, biologics, and radiopharmaceuticals).
  • The possibility to work in a company in which people, innovation, and entrepreneurship are the fundamentals of its success.

04.07.2020
Employee, 100%

Required minimum profile

  • 2 to 5 years of experience in managing Clinical Quality Management
  • Experience in managing tracking systems such as CAPAs database resulting from GCP audits (CROs, TMF, Investigational Sites and CSR) as well as deviations, changes tracking systems
  • Experience in maintaining quality SOP’s
  • Knowledge of GCP
  • Knowledge of GCP; Experience in maintaining quality SOP’s; Good practical experience in using validated electronic quality systems tools (TrackWise, Veeva, Ennov, etc)

Contact

Debiopharm International SA

CP 5911 /Chemin Messidor 5-7

1002 Lausanne

Phone: +41 21 321 01 11

Fax: +41 21 321 01 69


Debiopharm International SA

CP 5911 /Chemin Messidor 5-7Lausanne

Industry

Biotechnology / Chemistry / Pharmaceutical

Debiopharm International SA

CP 5911 /Chemin Messidor 5-7Lausanne

Industry

Biotechnology / Chemistry / Pharmaceutical
Salary

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