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Quality Assurance Inspector At GlaxoSmithKline Plc

Date Posted: 15/Sep/2013
Deadline: 26/Sep/2013

Job Purpose/Scope

The job exists to provide effective coverage for all quality parameters by monitoring the production activities and processes to achieve total quality assurance.

The job scope covers:
1) Independent quality audit of production processes, equipment, environment and products
2) Monitoring compliance with minimum Good Manufacturing Practice (GMP) and Environment, Health & Safety requirements 
3) Sampling and good inventory management of retained samples
4) Environmental monitoring of production and storage areas

Key Responsibilities

1) Undertake general audit of production processes, equipment and products (intermediate and finished) in compliance with Good Manufacturing Practice (GMP), GlaxoSmithKline Global Quality Policies (GQP) and National Regulatory Standards for Pharmaceutical production, to ensure consistent quality of products from batch to batch.

2) Implement strict compliance with current Good Manufacturing Practice to ensure quality standard of GSK products 

3) Document incidences of violations and product quality complaints in line with the Quality policy

4) Undertake final spot-check of finished products in Quarantine Store to ascertain quality Conformance and facilitate their timely release for sale

5) Implement withdrawal of retained samples for storage to ensure representative retention of Products before the expiration of such products 

6) Ensure retrieval of both retained samples and batch records in record time in compliance with GMP expectations on documentation

7) Undertake general quality inspection of finished goods/raw materials warehouse and other storage rooms to ensure finished goods/raw materials are kept at specified storage conditions

8) Undertake daily and weekly monitoring and recording of temperature, pressure differential and relative humidity of both manufacturing and storage areas to ensure that operations are carried out within specified condition/ specification

9) Partake in all trouble shooting activities that may occur on production lines to ensure that the cause is identified and solution found without compromising quality


Qualifications, Experience

1) B Sc in Sciences related degree preferably Pharmacy, Chemistry & Biochemistry. 

2) Must be IT literate

3) At least 2 years experience in a similar role



1) Sound knowledge of Good Manufacturing Practices (GMP). 

2) High level of integrity 

3) Sound knowledge of process audit techniques

4) Ability to cope with pressure

5) Good interpersonal skills



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