وظائف شركة فايزر للادوية Pfizer Egypt
Supply Chain Market Operation Officer
Governance &
internal organization
Support timely implementation of all applicable Product Quality SOPs (issued by
SCMOQ) within the PCO.
Ensure that all relevant PCO colleagues are appropriately trained in the Product
Quality SOPs.
Assess new quality system and local regulatory requirements to enhances and
align local systems and processes when required.
Conduct and document periodic assessments to determine if a revision,
retirement, administrative change or no change is required for the Product
Quality SOPs (issued by SCMOQ) within the PCO.
Quality Metrics
Collect data and report quality metrics for PCO operations to allow quality
performance assessment.
Together with the SCMOQ market lead, assess quality performance to identify
trends and improvement opportunities.
Participate in the PCO quality management reviews and follows-up for the
recommended actions, when required.
Product
Complaint Handling
Reporting complaints if any to AFME-HUB team withing the defined timeline.
Quality oversight on Local Relabeling operations
Ensure that relabeling sites have been trained and approved before performing
any relabeling activity.
When required, ensure that the relevant Regulatory approval for the relabeling
activity has been obtained by the regulatory team.
Complete the required documentation and obtain the necessary approvals from
Pfizer relevant functions.
Oversee the process of relabeling and review operation related documents.
Ensure SCMOQs release (as applicable) of the relabeled product according to
Pfizer and local requirements
Market Action
Attend, as needed (as back-up for example), Area Quality Review Teams (AQRT)
meetings, as PCO representative, to provide the local perspective on the issue
at hand.
Support to provide the local perspective on the issue and draft the AQRT
Executive Summary for issues originating under the responsibility of the PCO.
Support the local implementation of actions identified during Area Quality
Review Team (AQRT) meetings, e.g. recalls, communication with Regulatory Agency,
local corrective/preventive actions
Quality agreements
Develop, negotiate and maintain up to date quality agreements with all
affiliates, GMP/GDP distributors involved in repackaging, storage and
distribution activities
Quality risk management
Participate as risk leader or in the risk management committee for any opened
risk with PCO
Manage the opened risk and tracking the required approval
Updated risk tracker and archiving the risk assessment report as required
Qualifications/ Skills
Years of
experience: 0-3 years in the Pharmaceutical or related regulated industry
Technical skills:
Has an appropriate education in science or quality topics; Bachelor's degree,
Pharmacist, Engineer.
Has basic knowledge of the Quality principles, concepts of Quality and basic
technical skills
Has basic knowledge about Quality Systems (Change Control, deviations, complaint
management, documentation management, audits, inspections, etc.)
Able to Participate effectively in cross-functional team
Analytical skills
Excellent level in English
Soft skills/ Management & Leadership Skills
Self-motivated, Business acumen
Acts Assertively
Grows Self
Accountable
Change Agile
Self-Awareness
Planning & Organizing skills
Able to make decisions within guidelines and policies
Success criteria
To use new
ideas and knowledge with increasing frequency, begins to explore and apply
ingenuity to experimentation.
Able to work in ambiguous situations as part of a Work Team
Applies technical skills to achieve assigned tasks
Has effective communication, writing and negotiation skills
Able to align with global strategies
Efficiently represents Quality Compliance positions
