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Quality Assurance Control Manager Pharmaceutical

Eingestellt von Edelway

Gesuchte Skills: Support, Draw, Design

Projektbeschreibung

Hi All,

Edelway is a Swiss company active in Pharmaceutical and IT Recruitment field.

We are recruiting for a global pharmaceutical company based in Basel, Switzerland.

The role is Quality Assurance - Quality Control Manager.

It will be a long term contract with great salary expectations.

Your main tasks will be:

Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures. Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall TRD-Biologics strategies and goals.

Basic Major Activities

1. Actively participate in teams, projects, networks and/or platforms. Fulfill all related tasks and responsibilities related to own discipline.
2. Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s).
3. Design plan and perform scientific experiments/measurements, perform and contribute to project related scientific/technical activities (eg interpret results, evaluate data, draw relevant conclusions and write reports
4. Meet quality, quantity and timelines in all assigned projects, networks and/or platforms.
5. Actively participate in budget forecast, grant preparation and tracking of invoices. Demonstrate cost awareness in all assigned projects and/or networks.
6. Advise team members and work according to appropriate SOP's, GMP, HSE, ISEC and Novartis guidelines.
7. Interpret results, evaluate data, draw relevant conclusions, write reports.
8. Contribute to risk analyses and/or peer review and process challenge meetings.
9. Generate scientific documents to hand over to internal and/or external partners (TechOps, authorities, external companies)
10. Actively support generation of international registration documents. Interact with authorities where appropriate.
11. Interact/collaborate with Research and/or other functions to facilitate transfer of knowledge and deliveries of DS and/or DP.
12. Actively contribute to team goals.
13. Contribute to evaluation of new scientific technologies/equipment and prepare CAR and USR if applicable.
14. Coach/lead team members: support objectives setting, performance evaluations and development planning discussions with team members where appropriate. Participate in recruiting process if applicable.
15. Ensure all own activities are aligned with overall drug development process.
16. Strategic and scientific contribution to Networks, target achievements according to network charter and annual objectives
17. Provide efficient and robust processes for the manufacture and/or analysis of inter-mediates, drug substance and drug product as per own discipline.

Key Performance Indicators

1. Adherence to costs, quality, quantity, and timelines for all assigned tasks.
2. Adherence to standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards.
3. Feedback from other team members/leaders.
4. Refer to annual individual and team objective setting.
5. Measurable contributions to increasing efficiency and productivity in the work related to assigned projects.
6. Outcome of risk assessments, audits and inspections

If this could match with your profile please send me your CV at (see below)

Projektdetails

  • Einsatzort:

    Basel, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    Long Term

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Edelway