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Senior Quality Assurance Associate (Dev.) At Viatris Egypt

 Senior Quality Assurance Associate (Dev.) At Viatris Egypt

Senior Quality Assurance Associate (Dev.) At Viatris Egypt




Cairo,Egypt

Every day, we rise to the challenge to make a difference and here’s how the Senior Quality Assurance Associate (Dev.) role will make an impact:

Position summary

Ensure that GMP standards, as they apply to the individual products and the site, are in compliance with Viatris and regulatory standards.
Ensure that appropriate systems are in place to meet or exceed the requirements of the company and the regulatory authorities for the quality of the products manufactured on site.
Job Specific technical/Functional/Professional Competencies:

Ensure that GMP standards, as they apply to the individual products and the site, are in compliance with Viatris and regulatory standards
Preparation of monthly quality metrics to follow-up the performance of deviations handling system.
Act as “Deviations Handling system” process owner through following;
Responsible for performing quality review and impact assessment of assigned deviations as Quality point of contact.
Support opening investigations, conduct interviews and walking the process. Ensure that each confirmed case is investigated appropriately including ensuring investigation timelines are met and that appropriate pre-work is done on the case to enable an investigation with appropriate quality outcomes including a well written case summary (meets defined quality standards) which can be used in a regulatory inspection.
Responsible for follow up and approving of the Corrective Actions/Preventive Actions generated from deviations.
Act as Quality POC for assigned investigations.
Delegate for Deviation SH activities.
Responsible for preparing the “Area Quality Review Team Reports” for issues/deviations that require AQRT attention.
Annual deviations trending.
Support in the OBW for I initiative (One Best Way for Investigations) in VIATRIS Cairo through following;
Actively performing routine investigation system assessment (IUT) and analysis of the site investigation system to discuss opportunities regularly with SIL / QA Section Head.
Report PHP (Viatris Human   performance) utilization monthly to SIL / QA Section Head.
Follow Up over site IMSc (Investigations Maturity Scale) action plan and discuss completed actions / constraints with SIL on monthly basis.
Participate regularly and contribute to global discussion groups (PHPCIG, MINE meeting, ASK-MINE, others).
Work as needed with QS&C (QSSS/TL&C) SME’s to keep up to date with activities regarding the Investigations system.
Share in the preparation of quality-related audits conducted by Corporate and regulatory agencies.
Work with the appropriate people from both the quality and operational organizations develop a corrective action. Ensure their investigations are conducted with a strict adherence to appropriate quality and compliance standards.
Responsibility for compliance with Viatris Quality Standards.
Responsibility for compliance with Viatris Quality Standards
Share in the preparation of the issues that require SQRT attention.
Member of the Internal Audit Team responsible for sharing as a lead auditor in the site’s internal audit campaigns.
Development of various risk assessments.
Responsibility for implementation of Data integrity program in the relevant work area and Insure following up ALCOA principles all over operations.
Active implementation of Notification to Management procedures.
Responsibility for compliance with Viatris Quality Standards.
Experience and Knowledge 

A Bachelor’s degree in scientific field or equivalent pharmaceutical experience.
A minimum 3 years of experience in CAPA, investigations, or manufacturing quality assurance experience with a strong technical background in a cGMP and Quality environment.
Have a fundamental understanding of the investigation process as it applies to manufacturing issues.
Have detailed understanding of the processes and systems involved in the manufacture of Solid Dosage Forms and Semi-Solids pharmaceutical.  Be able to use that knowledge to investigate process deviations and atypical results and identify root cause.
Experience with word-processing, spreadsheet and presentation software (e.g. MS Word, Excel, Access).
Experience using data analysis computer tools and statistical analysis is preferred.
Experience in PQS/WHO/PQS requirements.
Experience with relevant QTS modules.
QRM Practitioner.
PHP Practitioner.

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