Multi Care Egypt for Pharmaceutical Industries is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, gender identity or expression, age disability, or other characteristics protected by prevailing regulations, practice or customs/traditions.
Multi Care is a well-established Pharmaceutical Company with diversified scope in both manufacturing and marketing of pharmaceutical products, supplements, cosmetics, and medical devices. Multi Care has +23 years of prominent existence in the local market and has almost +69 products marketed and more to come through the pipelines. Multi Care Egypt for Pharmaceutical Industries is the manufacturing facility which located at the Industrial Zone – New Cairo and its HQ is close by the facility as well in New Cairo.
We are one of the fast-growing Pharmaceutical Companies in the market which has strong ambition and aspiration to be one of the key players not only in Egypt but also within the region.
Our international alliances are effective in different countries, including Saudi Arabia, United Arab of Emirates, India, and New Zealand with future aspiration to extend more business associations and affiliations in near future to further markets. Recently Multi Care Poland has been launched which will be the entry port of the business to the European Union (EU).
Vacancy:
We are recruiting a Methodology & stability Manager to take the lead of the function as per the following details:
Designation: Methodology Manager
Bricks : Manufacturing Facility - 3rd Settlement - New Cairo
Grade: s Mm01/s Mm03
Reporting to : Plant Manager
Job Purpose:
Serves as focal point of contact for all stability related actives and represents the team in vis-à-vis cross functional meeting with opinions, views and recommendation concerning the practice
A. Essential Duties and Responsibilities:

• Follow-up development of the method of analysis of new drug molecules suitable for routine work of QC
• Development of stability-indicating assay of pharmaceutical products
• The validation of all the developed methods of analysis
• Solving any problems encountered in all the developed methods of analysis
• Performing analysis in the accelerated stability testing of R & D batches
• Documentation of MOA
• Analysis of formulation trials performed in the Formulation section
• Responsible for compliance with a quality integrated system for quality, environment, health, and safety in relation to his job and duties
• Comparative invitro analysis required for R & D trials
• Stability follow up (accelerated ,long term and ongoing)
• NODCAR files and Stability files for required products
• Lead activities further to analytical method to develop new or enhanced methods of analysis
• Conduct stability studies including preparation of stability plans, implementation of the study and related physical and chemical tests as well as preparing final stability reports including analysis of data & findings
• Take the lead in transforming business objectives into research practice and accordingly plan and delivers results of that association
• Keep updated on matters of new releases of literature and publications and scientific papers to keep abreast of changes in processing methods of analysis and stability
• Recommend the requests for new laboratories or laboratory equipment and instrumentation to serve expanding operational requirements
• Analysis of formulation trials performed by R & D Formulation Team
• Ensure the new product analysis results conform the product specifications
• Research and hence create new analysis method of products to be registered and launched in accordance with regulatory requirements and quality assurance systems
• Prepare & present the planning and development of survey instruments, guidelines and procedures to collect required data
• Strict adherence and compliance with a quality integrated system for quality, environment, health, and safety in relation to his/her job and duties
• Review Analytical Method Validations to ensure the accuracy of the proposed method of analysis

B. Qualification/Knowledge/Experience:

• Level of education: Life Science Degree (Pharmacy, Veterinary or Science)
• Experience : 6 experience of Pharmaceutical Stability and Methodology with people management capabilities
• Language : Reasonable English proficiency is mandated
• IT Literacy : Basic knowledge of MS-Office

C. Competencies and Behaviors:

• Professional leadership and influential skills
• Excellent analytical thinking
• Striving for continuous improvement
• Planning and prioritizing: ability to identify needs to be done and to develop an appropriate action plan in order to accomplish an objective and to monitor progress against it
• Able to cope with stress and change
• Impact and influence: the ability to convince, persuade others to a point of view
• Teamwork and co-operation: the willingness to work co-operatively and supportively with your colleagues. Developing positive, open working relationships in order to solve problems and to achieve business goals

What we offer:
With us, there are always opportunities to break new ground.
We empower you to fulfill your ambitions, and our diverse businesses offer various career moves to seek new horizons.
We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life.
Join us and bring your curiosity to life!
You love a good challenge. You are the first to roll up your sleeves and work with relentless energy until you solve the unsolvable, beat the unbeatable and you always come out on top. Passable doesn't cut it - you've got fire in your belly to learn more, do more and be more. For you, the sweetest success is shared success and you're known for your good nature.
You'll fit right in at Multi Care Egypt for Pharmaceutical Industries where we surround ourselves with the most talented and agile professionals in the industry, but we check our egos at the door.
Job Type: Full-time