Job Description

Why Patients Need You Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer's mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes.

What you will acheive we need a profile that take in charge : -production documentation - follow up and closure of investigations, actions audit actions follow up of continous improvement projects

how you will acheive it ?

Investigations /change controls /actions shall be responsible for the closure of Production investigations and actively participates in the proposal of effective CAPAs to avoid recurrence, .Participates to follow up production Change Control and the monitoring of actions, follow up closure of Audits actions

Training 1. development of the annual training plan; 2. Monitoring and follow up on trainings metrics

Documentation 1. update procedures 2 track expired documents and have a plan of action 3 perform Data integrity assessments for prodcution equipements

Continuous improvement projects

1. follow up of Continious improvement projects 2. establish connection between all Improvement elements and collect data to analyse loss root cause and support team to find good projects and Actions

Qualifications Must-Have

Master assurance qualité or equivalent

Ability to quickly assess and assimilate technical data and conduct thorough investigations.

Excellent written and verbal communication skills.

Production and/or Quality Assurance experience.

Understanding of Lean tools.

Thorough understanding of current GMP (Good Manufacturing Practices) and regulatory aspects.

Work Location Assignment: On Premise Position based in El Jadida

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

Manufacturing

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