OQ Seal Inspector at GSK | GSK vacancies | Fresh Graduate | pharmaceuticals jobs | recruitmentblogs
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 application of GMP measures during validation batches and planned changes.
*Ensure that GMP standards are followed up in the facility / WH / Utility to serve manufacturing process.
*Handling and management of batch records & OQ quality files in documentation room as per GMP requirements.
*Revise Quality technical documents according to Corporate Standards, such as GQP’s, and , GQMP’s, This includes batch manufacturing and packaging documents, specifications, SOPs and bills of materials.
*Handle the performance review of Quality Systems within value stream.
*Conduct IPC along with manufacturing, packaging process to ensure quality level maintained.
*Provide Quality oversight to the three shifts of production (when required).
*Coaching operators to ensure that quality mindset is embedded in their day to day activities.
2- FG Sealing
*Conduct the sealing process for finished good.
*Direct interaction – handling – communication with MOH authorities.
Knowledge/ Education / Experience Required:
-University Bachelor's degree from faculty of Pharmaceutical Sciences
-0 to 2 years of experience
-A previous experience in similar role in a pharma industry is an advantage
-Good knowledge of GLP and GMP requirements
-Good command of the English language
-Good Computer Skills
-Excellent communication and interpersonal skills
-Actively seek to improve processes, controls and expand effectiveness and efficiency
-Self-motivated with Good prioritization and organization skills
-Ability to work independently and as part of a team