القائمة الرئيسية

الصفحات

 OQ Inspector Non Sterile At GSK 

OQ Inspector Non Sterile At GSK


Job description

Site Name: Egypt - Giza 


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:


1. 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.

2. 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.

3. 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.

Knowledge/ Education / Previous Experience Required:


University Bachelor’s degree in pharmaceutical sciences.

2 to 3 years of experience.

Good knowledge of GLP &GMP requirements.

Good command of the English language.

Good computer Skills with Microsoft Word and Excel.

Excellent communication and interpersonal skills.

Apply here

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