QUALITY CONTROL MANAGER ONCOLOGY - ALGERIA

International Permanent INR8,240,150 - INR9,888,181 per year View Job Description
You will be responsible of managing, reviewing and overseeing relevant quality control (chemicals & microbiological) activities and practices by ensuring integrity and traceability of all generated data in accordance with the current SOPs and contributing to the development and implementation of quality standards /& principles.
  • Oncology
  • Attractive package

About Our Client

Our client is a new oncology products manufacturer in Algeria.

Job Description

You will be responsible of the following tasks:

-Supervise the implementation of the Quality Control function plans, and ensure their compliance with client quality system

-Develop the quality control function's work plan; assign work activities, projects and programs, review and evaluate analytical methods and procedures, and directing the quality control activities to serve the QC department objectives.

-Ensure that qualification/validation and maintenance of the QC Laboratory premises and equipment/instruments are appropriately performed

-Develop and maintain quality control procedures by ensuring completion of all tests, studies, reports and investigations in an accurate, effective and timely manner

-Review and evaluate all data generated according to written procedures and recommend on the release or reject of the analyzed items (raw materials, packaging materials, intermediate, bulk and finished products)

-Contribute for evaluation and qualification of vendors of raw materials and packaging materials.

-Inform all involved functions of any rejects and non-conforming results related to raw materials, packaging materials, finished products, and any other area monitored by QC testing

-Lead the execution of investigations on relevant QC issues (OOS/OOT/deviations),verification results and determine corrective and preventive actions as per defined SOPs

-Develop and validate the analytical methods in accordance with the current regulations and apply the latest technical methods

-Validate the analytical test procedures, specification sheets, SOPs (pharmacopoeia and In-house). Review and approve documents related to QC function activities (procedures, protocols, reports, etc.)

-Establish and maintain a tracking and trending system of QC issues (OOS /OOT)

-Conduct performance appraisals for subordinates according to scheduled plans and recommend necessary actions as per the applied practices

-Co-ordinate technical audits of the QC Laboratory to determine the analytical quality systems are yielding the highest quality information and to ensure that the analytical instrumentation is functioning properly and calibration and servicing is as per schedule.

The Successful Applicant

5 years of experience in a related position, of which at least 2 years in supervisory position.

10 years (or more) in a similar position within pharmaceutical company.

What's on Offer

Salary+housing+car+health insurance+benefits

Quote job ref
JN-022025-6671749

Job summary

Function
Healthcare & Life Sciences
Sub Sector
Manufacturing / Quality
What is your area of specialisation?
Healthcare / Pharmaceutical
Location
International
Job Type
Permanent
Job Reference
JN-022025-6671749

Diversity & Inclusion at Michael Page

We don't just accept difference - we celebrate it. We encourage applicants from all backgrounds to apply for this role and are committed to building inclusive, diverse workplaces where everyone can thrive. If you require any support or reasonable adjustments during the recruitment process, please let us know.