وظائف شركة جلاكسو سميثكلاين للادوية GlaxoSmithKline مطلوب مهندسين

وظائف شركة جلاكسو سميثكلاين للادوية GlaxoSmithKline مطلوب

مهندسين

Engineering Validation Section Head

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:

1 - Executing the Validation Lifecycle for all new and existing GxP systems according to QMS
Determine the impact of the equipment/system on GMP processes through Compliance Determination
Create and execute validation lifecycle documentation such as (MBP, PRA, CD, URS, DQ, IQ, OQ, PQ, VSR) as per CSQMS, AEQMS, ITQMS depending on the type of system
Verify the Validation of excel sheets & Validate excel sheets (If necessary)
Perform Periodic Validation Review to maintain and review the validated status of the systems
Decommissioning of GxP systems and Excel Sheets
2 - Acting as the CSV Lead for Giza Site responsible for:
ATR & Back up Process Owner
Admin user for all lab equipment
Extract audit trail and review with lab/production teams the content and ensure the gaps are closed (Trackers)
Back up the lab/production equipment software and data
Review the DI assessment after completion by system owner and mitigate the gaps
Record ATR and Back up KPIs and report to DI champion
Raise capability of system owners for effective review of audit trail
Review ATFA and ensure that is reflected in ATR tracker
Review access maps for lab/production equipment
System owner for password Manager Software

3 - Responsible for planning and prioritizing the validation activities through the Validation Master Plan

Maintain and review Site System register to ensure all mandatory fields are entered and the systems are accurately recorded.
Reflect the outcome of (SSL) site system list into (VMP) validation master plan
4 - Participate/ Coordinate the execution of validation testing with other departments and suppliers
5 - Confirming DI requirements are met in the design of new and existing system against ITMS , QMS &SOPs
Management of data backups system passwords
Managements of users and administrative functions for the different systems
6 - Responsible for the continuous improvement and standardization of the validation activities/documentation
Maintaining a robust documentation and archival system
Maintain an inspection ready status ahead of any internal and external audits for validation activities
7 - Supporting the validation capability of the site
Delivering of periodic validation training for all site staff

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

Bachelor’s Degree in Engineering
Minimum of 5 years of experience in a similar position
Good knowledge of data integrity requirements​
Good planning and coordination, problem solving and time management skills.
Strong Analytical Skills & Team Work
Good interpersonal and communications skills.
Ability to work under stress and to manage conflicting priorities.
Production Knowledge & experience in sterile operations is a plus.
Excellent command of English language

Apply Here