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Quality Assurance Supervisor


Casablanca, Casablanca-Settat 20250
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Job Details

Position : Quality Assurance Supervisor

Department : Quality Operations

Direct manager : Quality Operations Leader

Starting date : immediate

Criteria for the position

Main missions

- Monitoring and supervision of the Quality Assurance activities.

- Supervision of the Quality Assurance department staff.

Qualifications / Professional Experience / Skills Required

- University degree in Pharmacy, Engineering Chemistry. Desired specialty.

- Experience of at least 3 years in Quality Assurance, Quality Control, production in pharmaceutical industry.

- Very good knowledge of GMP (Good Manufacturing Practices)

- Good knowledge of manufacturing operations, packaging and testing of medicinal products.

- Good knowledge of, utilities, HVAC and water Systems

- Good on verbal and written communication.

- Fluent in French and English.

- Management of multidisciplinary team.

- Good spirit of synthesis, taking initiative, calculated risk and innovate

- Have excellent organization of work and an effective filing system.

- Ability to plan, implement actions to achieve the goals.

- Ability to withstand the pressures and potential crises.

- Sense of responsibility and maturity for decision making.

- Commitment to Company missions, Values, and Behaviors.


- Release of finished product batches

-Quality Review of batch records

-Participation in the decision on the status of batches

- Organize and track the product annual review system

- Working closely Production / Engineering / QC / Supply / Procurement departments to ensure Quality management systems: Deviations, Changes, Complaints, analytical results out of trend and out of specifications;

-participation in their treatment (investigation and/or assessment and

establishment of CAPA Plans) and their approval on timelines

in accordance with procedures.

- monitor achievement of established action plans

- Manage the qualifications and validation with relevant departments Production /

Engineering / Quality Control / Supply / Procurement

- Review qualification and validation plans.

- Review qualification and validation protocols and reports.

- Ensure quality ongoing activities of manufacturing and packaging process:

- Line clearance Approval.

- Line starting Approval.

- In process control.

- Manage the training system.

- Provide quality trainings.

- Ensure the implementation of the training and on the job training programs.

- Ensure the register and monitor of training programs achievements.

- Ensure the management of documentation system

- Preparation and implementation of new procedures.

- Review and approval of procedures submitted.

- Updates department procedures.

- Compliance with procedures.

- Ensure, in collaboration with relevant departments, Compliance to Quality Standards

- Conformity Assessment.

- Monitor the Plan of action to ensure compliance.

- Ensure internal audits, suppliers, and contractors

- Participation in Establishment of the audit program.

- Participation in audits.

- Approval and Monitoring audits Plan of actions.

- Monitor the Quality indicators (Metrics)

- Participation in the establishment of Targets.

- Develop trend analysis.

-Participate in improving Metrics.

- Ensure continuous improvement of existing systems and establishment of new QA systems.

- Ensure temporary assignments for the department.

Anyone wishing to apply for this position is requested to submit his resume and a cover letter.superviseur AQ

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