Quality Vacancy At Viatris Egypt
Title:Quality Operations Senior Associate
Key responsibilities for this role include:
Administrative & Inventory tasks:
Manage supplier/vendor communications for QO purchases and request quotations.
Issue purchase orders for quality operations consumables
Track purchases on-time goods and services delivery & receiving.
Keep Quality Operations organizational chart & distribution list updated.
Arrange and schedule interviews for QO vacancies as needed.
Arrange QO town halls and meetings, including reservations.
Point of contact for site meals committee and transportation committee on behalf of QO
Support in preparing for hosting visits and audits
Responsible for Overtime, daily attendance & sick leaves follow-up of QO department
Responsible for stock, inventory management and keeping of stationery, reagents, consumables, and glassware, including periodic checks.
Documentation tasks:
Implementation of documentation rebranding of MCD (materials control documents) related to QO for testing methods and specifications.
Perform official printing of QC batch records & QO Logbooks requested for testing activities.
Generation, controlling and reconciliation of logbooks.
Perform official printing for requested QO records.
Reviewing and checking QO Logbooks completeness
Issue contracts in LCM for highly purchased suppliers for QO purchases
Complete relevant commitment actions as required (CCR Actions and CAPA Actions).
Transporting and controlling samples delivery to EDA as needed
Performing and documenting destruction visits to external service providers with EDA representative as needed
Responsibility for implementation of Data integrity program in the relevant work area and ensure ALCOA+ principles all over operations.
Active implementation of Notification to Management and Critical Quality Notification procedures.
Responsibility for compliance with Viatris Policies and Quality Standards.
The minimum qualifications for this role are:
Bachelor’s degree in Pharmaceutical Sciences or Science
3 - 5 years’ experience in pharmaceutical manufacturing environment is required
Good Documentation Practices knowledge.
QC Knowledge or Experience is a plus.
Data Integrity and ALCOA+ Knowledge
Good command of English both written and spoken.
Knowledgeable with interpersonal learning.
Communication, teaching and coaching skills.
The essential personal qualifications for this role are:
Strong interpersonal and communication skills
Accurate and detail-oriented
Task and results-oriented
Gets things done