Operational Quality Officer

Site Name: Egypt - Cairo
Posted Date: Nov ‎2 ‎2022

Are you a pharmacy or science graduate who is energized by the opportunity to
kickstart and progress their career within the Operational Quality team of one
of the leading pharmaceutical companies worldwide? If so, then this
opportunity may be the one for you to consider.
As an Operational Quality Officer, you will be responsible to follow up
adherence to OQ system and GMP in production areas, check batch-related
documentation, and provide reports about quality performance against approved
standards.
This role will provide YOU the opportunity to lead key activities to
progress YOUR career, these responsibilities include some of the following:
* Revise Quality technical documents according to Corporate Standards, such as GQP 's, GQMP's and FPG's. This includes batch manufacturing and packaging documents, specifications, SOPs and bills of materials.
* Ensure proper sampling of intermediate, bulk and finished product batches for routine testing, validation practices and cleaning samples.
* Follow up application of OQ measures in production areas and check compliance of in-process testing.
* Ensure application of OQ measures during validation batches and planned changes.
* Monitor calibration of production equipment and IPC testing instruments.
* Review batch related documentation for completeness, correctness and compliance to approved standards.
* Report any observed incidents during routine production and follow up its correction and corrective action.
* Ensure that GMP Standards are followed properly in the Warehouse, Dispensing and manufacturing areas and during the manufacturing and packaging processes.
* Handle deviations, complaints and OOS & OOT in coordination with area owners and ensure implementation of CAPA and closure within required timeline.
* Team member in self inspection and provide Quality inputs in CCRs.
* Support EHS & GPS implementation in managing different activities.
* Ensure identification and rejection of non-conforming materials/products according to GMP standards.
* Responsible to participate in Self Inspection program within OQ department to confirm department adherence to LSOPs and policies.
* Simplify the production process with meeting GSK quality standards
* Coaching operators to ensure that quality mindset is embedded in their day-to-day activities.
* Handling PCCE incidents in the VS Areas.
* Responsible for and ensure proper implementation of ALCOA+ principles Ensure proper handling eject and reject Activities in VS areas
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our
goals:
* Bachelor's degree in Pharmaceutical Sciences or Science.
* ‎1 - ‎3 years of experience within a similar field.
* Up to date knowledge of current GMP, EDA Regulatory requirements, GSK QMS System.
* Excellent documentation and report writing skills.
* Excellent verbal and written communication skills.
* Familiar with IQ, OQ, PQ, facility, utilities, Equipment and Strong experiences in cGMP/GLP compliance activities.
* Good command of English language (spoken and written)
* Good Computer (Word and Excel) and communication skills
* Knowledge of EHS and GMP requirements
Why GSK?
At GSK, we have already delivered unprecedented change over the past four
years, improving R &D, becoming a leader in Consumer Health, strengthening our
leadership, and transforming our commercial execution. Now, we're making the
biggest changes we've made to our business in over ‎20 years. We 're on track
to separate and create two new companies in ‎2022: New GSK with a leading
portfolio of vaccines and specialty medicines as well as R&D based on immune
system and genetics science; and a new world-leading consumer healthcare
company of loved and trusted brands.
With new ambition comes new purpose. For New GSK, this is to unite science,
talent and technology to get ahead of disease together - all with the clear
ambition of delivering human health impact; stronger and more sustainable
shareholder returns; and as a new GSK where outstanding people thrive.
Getting ahead means preventing disease as well as treating it. How we do all
this is through our people and our culture. A culture that is ambitious for
patients - so we deliver what matters better and faster; accountable for
impact - with clear ownership of goals and support to succeed; and where
we do the right thing. So, if you 're ready to improve the lives of
billions, join us at this exciting moment in our journey. Join our challenge
to get Ahead Together.
GSK is a global biopharma company with a special purpose - to unite science,
technology and talent to get ahead of disease together - so we can positively
impact the health of billions of people and deliver stronger, more sustainable
shareholder returns - as an organisation where people can thrive. Getting
ahead means preventing disease as well as treating it, and we aim to impact
the health of ‎2.5 billion people around the world in the next ‎10 years.
Our success absolutely depends on our people. While getting ahead of disease
together is about our ambition for patients and shareholders, it's also about
making GSK a place where people can thrive. We want GSK to be a workplace
where everyone can feel a sense of belonging and thrive as set out in our
Equal and Inclusive Treatment of Employees policy. We're committed to being
more proactive at all levels so that our workforce reflects the communities we
work and hire in, and our GSK leadership reflects our GSK workforce.
Contact information:
You may apply for this position online by selecting the Apply now button.
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