Site Name:* Egypt - Giza - Giza
Posted Date: Jan 19 2023
Job Purpose
Ensure safety of working environment for all employees. Ensure maintenance of
all quality standards on all ongoing lab activities and our compliance with
regulatory expectations. Ensure elimination of waste during ongoing
activitiesto improve cost improvement. Ensure successful planning for all
activities and successful execution of plans to meet required supply dates.
Ensure proper qualification for all levels on all role being undertaken.
Ensure proper positive integrate transparent patient focused and people
respect oriented culture in working environment
Key Responsibilities
* Checking for all day to day activities and make equilibrium of workload to maximize utilization of resources. Cope with any change according to business need.•
* Ensure secured supply of Analytical Lab. facilities, routine and stability analysis requirements, spare parts, preventive maintenance contracts and implementation of modern analytical Lab.
Techniques.•
* Ensure the Validation of new lab. Techniques, test methods, new instruments,
* •Ensure the implementation of up to date SOP's m line with changes to the source documents, such as GQP's, GQG's, FPG's or regulatory documents and assess the related performance via periodic trend evaluation, annual product review, evaluation reports, monthly reports and case studies. In addition, ensure that EHS Policies and Procedures are implemented in the Analytical labs and all other related functions.•
* Verify and follow up implementation of cGLP, cGMP Pharmacopoeia and new Policy requirements and follow up the required actions that should be taken after internal and external audits•
* Ensure satisfactory training of subordinates on any new or updated procedures and information.
* Providing the necessary Technical support to interpret, decide and evaluate any problem related to processing areas, corrective/preventive actions.•
* Train subordinates on any new or updated procedures and information. Provide the necessary Technical support to interpret, decide and evaluate any problem related to processing areas, corrective/preventive actions.•
* Approve the investigation in case of out of limits results, escalate and communicate critical issues, advising local management, where necessary, and ensure that actions needed have appropriate priority.•
* Achieve and Cooperate continuous improvement program through:•Planning, organizing and scheduling business need•
* Performing new tasks/projects•
* Achieving Lean Lab. approach for all analytical Lab. activities•
* Co-ordinate with other departments (e.g. Planning, Quality Assurance, Production, Validation, Procurement) to achieve a positive tendency of workload/work quality according to Company demand.•
* Manage QC lab budget, stock management and control.•
* Ensure correct calculation of chemical. Lab. Performance and lab Efficiency.
* Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our
goals:
* Bachelor 's Degree Pharmaceutical sciences or equivalent
* 8 years of experience
* Solid experience in Quality and/or Production functions is a must.
* People management experience is a must•
* Good Analytical and influencing skills.•
* Good command of English and Computer skills •
* Very good communication skills.•
* Up to date knowledge of current GMP, MOH regulatory requirements, GSK QMS System.•
* Excellent documentation and report writing skills.•
* Self-motivation, empowerment and adaptation to business changes.•
* Strong prioritization and organization skills.•
* Excellent verbal and written communication skills.•
* Familiar with IQ, OQ, PQ, facility, utilities, equipment and Strong experiences in cGMP/GLP compliance activities.•
* Able to demonstrate experience of managing diverse teams of professional staff and effective budgetary control against agreed targets.•
* Experienced in handling regulatory interfaces such as inspections
Why GSK?
Our values and expectations are at the heart of everything we do and form an
important part of our culture.
These include Patient focus, Transparency, Respect, Integrity along with
Courage, Accountability, Development, and Teamwork. As GSK focuses on our
values and expectations and a culture of innovation, performance, and trust,
the successful candidate will demonstrate the following capabilities:
* Operating at pace and agile decision-making - using evidence and applying judgement to balance pace, rigor and risk.
* Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
* Continuously looking for opportunities to learn, build skills and share learning.
* Sustaining energy and well-being
* Building strong relationships and collaboration, honest and open conversations.
* Budgeting and cost-consciousness
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.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment
agencies in respect of the vacancies posted on this site. All employment
businesses/agencies are required to contact GSK's commercial and general
procurement/human resources department to obtain prior written authorization
before referring any candidates to GSK. The obtaining of prior written
authorization is a condition precedent to any agreement (verbal or written)
between the employment business/ agency and GSK. In the absence of such
written authorization being obtained any actions undertaken by the employment
business/agency shall be deemed to have been performed without the consent or
contractual agreement of GSK. GSK shall therefore not be liable for any fees
arising from such actions or any fees arising from any referrals by employment
businesses/agencies in respect of the vacancies posted on this site.
* determining, negotiating and agreeing on in-house quality procedures, standards and specifications * assessing customer requirements and ensuring that these are met * setting customer service standards * specifying quality requirements of raw materials with suppliers * investigating and s…
we are in need of quality control coordinator with 2 years of experience with CPHQ certification. Experienced in CBAHI and JCI regulations and accreditation. Responsibilities Implement and follow up all quality policies and regulations in the company medical and non medical.
**Site Name:** Saudi Arabia - Jeddah **Posted Date:** May 23 2022 ** Job Purpose** Develops and implements programs to establish and maintain quality standards of existing products, and internal systems and processes. Develops policies, procedures and methods to check product, material, compon…
* **Quality policies and programs** * Develops, implements, monitors, maintains and improves the quality policies and the quality control, HACCP and Food Safety/Food Defense and similar programs, in coordination with the manager(s) of production, supply chain and other relevant areas, according t…
Essential Functions Statement(s) Comply and ensure compliance with safety and environmental guidelines, policies, and regulations. Maintain ongoing contact with staff members, third party personnel, quality consultants, and customers. Maintain a continual improvement of the product & process throug…
_Our People & Places Solutions business - reinforces our drive to improve the lives of people everywhere and epitomizes the "why" of what we do - the tremendous positive impact and value our solutions bring to our communities and society as a whole. From facilities delivering life-saving therapies …
**POSITION SUMMARY** The Quality Control Manager (QCM) is responsible for implementing and evaluating the effectiveness of the Security Support Services (SSS), Area Support Group (ASG), Kuwait (ASG-KU) contractor Quality Control Plan (QCP). The QCM advises the Program Manager and in Country Project…
Job Title Quality Control Manager Job Code 9QCM Location Alexandria Posting date 23/05/2013 Description Industry: FMCG Minimum 20 years experience
**Quality Control Manager** **Are you passionate about Quality in Manufacturing?** **Do you enjoy taking ownership for quality requirements?** **Join our team** Our diverse and global team ensures that our customers have the products and services they need to perform effectively and safely. Our …
Our Client one of the leaders in the largest and most important **industry field Dairy** in **Libya** , is looking for well experienced candidates to fulfill the following positions: **Quality Control Manager** * University graduated in **Science and Food Engineering** * Minimum **5 years…