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23 déc. 2021 à 17h32   Autre   Rabat   32 vues
Détails de l'annonce
Why Patients Need You

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

You will be a member of Pfizers dedicated and highly effective quality assurance and control team. You will be responsible for providing operational support to Quality Control Laboratory. Your contributions will help Pfizer provide safe drugs to patients.

As a Team lead, you will be involved in leading work teams within your division, including the technical and financial resources of the team. Thanks to your technical skills, you will coach your direct reports on day to day activities. You will be relied on to solve complex problems within your area of expertise.

It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It
  • Manage multiple projects and ongoing work activities of within a work team and ensure agreed upon timelines are met.
  • Oversee and review/approve investigations, CAPA (Corrective Action and Preventive Action) and change controls.
  • Review laboratory data to ensure compliance with approved methodologies.
  • Build capabilities of the Process-Centric Team according to skills needs assessments.
  • Serve as a point of contact for issues related to quality control activities (Finish goods, Raw material/Packaging material, bulk and stability sampling and analysis).
  • Engage with business partner to identify areas of improvement across laboratory and core applications and processes.
  • Provide technical expertise and support to the QC laboratory for laboratory and core applications.
  • Manage review and approval of Good Manufacturing Practices {also cGMP} documentation, such as procedures, data and reports.
Qualifications

Must-Have
  • Bac + 5 in scientific studies
  • 3+ years experience in Pharmaceutical Industry
  • Knowledge of Good Manufacturing Practices {also cGMP} compliance requirements for Quality Control Laboratories
  • Leadership experience (direct supervision of a team or indirect leadership such as team/shift lead, project leadership, etc.)
  • Strong people management experience
  • Demonstrated skills in collaboration, attention to detail, and communication skills
  • Ability to handle complex and detailed situations with a focus on quality
  • Fluent in Arabic and French, and good level in English
Nice-to-Have
  • Laboratory supervisory experience preferred
  • Knowledge of Laboratory Information Management System (LIMS) and Microsoft Office
End Date Posting: 27 December 2021

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Quality Assurance and Control