Type d’emploi: Full-time

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le contenu du travail

Site Name: Belgium-Wavre
Posted Date: Jun 22 2021

Job Purpose

The LES (Laboratory Execution System) QC Microbiology & Sterility Assurance (Microbiology & Virology) supervisor contributes to implementation of LES activities through different teams of your Department. You guarantee implementation according to defined rules and to the program Roadmap.

To guarantee that implementation will be compliant (in alignment with QA partner) the role ensures the following:
  • Managing change (process, mindset, within the QC Microbio & SA Teams is a key success factor.
  • Being a QC Microbiology & Sterility Assurance representative for sharing /explaining QC Microbio & SA specificities to LES Implementation team.
  • Being an active member for key delivery process steps: Data collections, prototyping, Workbook validation (DCMA) and implementation activities (BCO).

Your Responsibilities
  • You support current QC Microbiology & SA supervisors and operators in delivering LES program/planning within QC Microbio & SA.
  • You act as key player during the project roll-out (Data collection, Prototypes, DCMA (= validation) and lab readiness (BCO). These activities will be executed according to LES processes (training will be provided by LES program Team) and laboratories priorities / planning adjustements.
  • You are a strong partner to laboratory and LES Implementation manager to build roll-out plan (time-line, WoW, team sizing,...) taken into account QC Microbio & SA Lab constraints.
  • According to LES Roadmap program discussed with teams and defined by LES Implementation managers, drives the roll out of the LES project through the different teams of your Department.
  • According to current guidance established by LES LSPOC (Documentation, training, archiving, change control,...) of the concerned process, implement the paperless project within your Department.
  • You escalade risks & problems, proposing action plans to LES Implementation Manager.

Why you?

Basic Qualifications

We are looking for professionals with these required skills to achieve our goals:
  • Master Degree.
  • Sciences with quality orientation.
  • Experience in analytics (experience in virology, bacteriology is a plus).
  • Position requires ability to understand business process management, and networking across the upper QC (QC Microbio & Sterility Assurance - virology) organization.
  • Good knowledge of Quality Process (Testing, Documentation, training, archiving, change control).
  • Min. 3 years of relevant experience in a quality QC department.
  • Deep Knowledge of cGMP (potentially Audit fronter).
  • Experience in change management
  • Experience in team management/stakeholder management 5-20 people.
  • Innovative thinking, open to change.
  • Ability to use IT tools-French & English skills.

Preferred Qualifications

If you have the following characteristics it would be a plus:
  • Ideally, has already participated to Lean initiatives, LIMS is a plus.
  • Li-GSK

  • Why GSK?

    Our values and expectations are at the heart of everything we do and form an important part of our culture.

    These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork.

    If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

    Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.

    Important notice to Employment businesses/ Agencies

    GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK’s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
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    Date limite: 31-12-2025

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