OQ Inspector Non Sterile At GSK 

Job Purpose

Follow up adherence to OQ system & GMP in production areas, Check batch–related documentation, and provide reports about quality performance against approved standards

Key Responsibilities:

GMP

Follow up application of GMP measures & std procedures in production areas and check compliance of in-process testing.
Ensure that GMP Standards are followed properly in the manufacturing areas and during the manufacturing processes.
Coaching operators to ensure that quality mindset is embedded in their day to day activities.
Deviations

Report any observed incidents during routine production, conduct required Investigation and follow up its correction and preventive action.
Conduct the RCA with the required time frame as per QMS with the responsible area owner and agree on the appropriate CAPA.
Complaint management, conduct RCA with responsible area owner and agree appropriate CAPA.
Handle deviation, complaints and OOS in coordination with area owners and ensure implementation of CAPA and closure within required timeline.
Other functions:

Conduct the OQ self-inspection to evaluate the department activities and agree on the action plans.
Attendance of change control process evaluates and approves changes, follow up and track required actions until the CCR implementation.
Support site achieving core & non GMP KPIs within strategy.
Update department SOP in accordance to Quality compliance requirements.
Team member in L1 and provide Quality inputs in CCRs.
Why you?

Basic Qualifications:

Education and Experience:

2-3 years of experience
BSC in pharmaceutical sciences
Good command of English (spoken and written).
Good Computer skills (Word and Excel).
Very good communication skills.
Knowledge of GLP &GMP requirements.

Apply here

تعديل المقال