El-Hussieny Mohamed Ibrahim

Address: Block C -El-Gamma Street –Nayla Khaton, Asyūţ,

71111, Egypt

Tel:
+201090774100
+201099007544
02-07-1981
asyut Email: drhus81@gmail.com
Na onality
Egyp an
Profile

SKILLS Dedicated and detail-oriented individual with a proven track record in the
pharmaceu cal industry.I am ac vely seeking a Produc on Manager
Leadership and Teamwork
posi on within a professional organiza on that values both its people and
Ability to Work in a Team the products it promotes. I aim to leverage my extensive experience and
Cri cal thinking and skills to contribute to the company's success to the fullest extent. With my
problem solving strong a en on to detail and passion for excellence, I am commi ed to
Ability to Mul task driving opera onal efficiency, maintaining high-quality standards, and
fostering a culture of con nuous improvement. I am confident that my
Crea vity
exper se in produc on management, team leadership, and adherence to
Decision Making regulatory requirements will make me a valuable asset to your
Adaptability organiza on. Let my dedica on and exper se help elevate your
organiza on's produc on opera ons.
Time Management

Effec ve Time Work Experience

Management
April 2020– date
Communica on Skills

Computer Skills
Produc on General Manager , CID Company , Asyūţ
Microso Office • Responsible for conduc ng annual product reviews.
• Plans produc on capacity in alignment with con nuous improvement
goals for manufacturing cycle me and labor efficiency.
• Inves gate and resolve manufacturing issues to prevent delays in mee ng
LANGUAGES
customer orders or project deadlines.
Arabic • Produces and maintains process documenta on, suppor ng training
English needs in machining, assembly, and inspec on processes.
•Specifies and implements improvements to enhance cost-effec veness,
manufacturing processes and procedures, material suitability, reject and
defect rates, and more.
HOBBIES • Maintains and supports Quality Assurance in the implementa on of
Traveling: Social valida ons and qualifica ons.
Networking and Social • Ensures that all products received and shipped from the site meet
Ac vi es: Reading required quality standards while maintaining compliance with GMP
Listening to Music standards.
• Manages quality systems, including devia ons and complaints.
• Assists in the management of on-site regulatory audits.
• Reviews Batch Produc on Records (BPR) and Standard Opera ng
Procedures (SOPs) to ensure smooth produc on opera ons.
• Reviews and issues the required quan es of materials needed for
produc on, according to the predetermined plan.
• Ensures readiness of equipment and machinery for opera on, following
set procedures for each product.
• Takes into considera on the availability of produc on materials and
ensures produc on is conducted according to pharmaceu cal and quality
standards.
• Supervises and monitors repor ng of any produc on machine
malfunc ons and coordinates with the maintenance department for
immediate repairs.
• Studies produc on problems and proposes solu ons without
compromising efficiency and the produc on process.
• Monitors and ensures op mal produc on in compliance with in-house
and regulatory limits.
• Drives con nual process improvement ini a ves.
• Sets plans for new machinery and produc on lines based on market
needs.
• Establishes a Training Program and regularly assesses its effec veness.

April 2015 — March 2019

Produc on Sec on Head , CID Company (Solids), Asyūţ

My responsibilities included: https://www.cvtemplatemaster.com

● Ensures that all employees are aware of their roles and

responsibilities,and provides the necessary support and development
opportunities to help them achieve their highest level of performance.
● Provides leadership and guidance to the divisional staff, fostering a
positive work environment and promoting teamwork.
● Organizes the rotation plan for employees, ensuring efficient allocation
of resources and coverage of essential tasks.
● Manages and arranges subordinate leaves, working days, and day-offs,
ensuring adequate staffing levels at all times.
● Recruits and coaches staff on professional knowledge and job-related
skills, fostering their growth and development.
● Sets up Key Performance Indicators (KPIs) to appraise staff performance
and monitor progress toward goals.
● Collaborates with other departments to fulfill assigned tasks and
achieve overall organizational objectives.
● In addition to the above responsibilities, also carries out other
production-related duties ... mentioned next.
 April 2009 — March 2015

Produc on supervisor , CID Company (Solids), Asyūţ

My responsibilities included : https://www.cvtemplatemaster.com

● Solid Dosage Form Department: Tablets, Capsules, Powders,

Compression Costing.
● Proficient in the preparation, compression, and coating of tablets.
● Experienced in the preparation and filling of capsules.
● Skilled in the preparation and filling of powders.
● Excellent experience in wet granulation and troubleshooting
granulation issues to maintain product yield.
● Proficient in film coating and sugar coating tablets of various sizes.
● Conducted cleaning validation of all production steps.
● Successfully carried out process validation for all products with positive
results.
● Responsible for the operation of new apparatus and machines.
● Performed Installation Qualification (I.Q.) and Operational Qualification
(O.Q.) for various equipment, including tablet compression
machines,Aeromatic F.B.D oven, blender mixer from Canaan Company,
and Korsch tablet compression machine (Korsch XL400).
● Great experience in operating and troubleshooting tablet compression
machines, adapting them for different types of powder.
● Responsible for the preparation, filling, and packaging of powders.
● Conducted process validation for powder products (lohydran,
rehydrozinc, entocid comp.).
● Arranged and managed the powder production line according to
company demands and sales requirements.
● Ensured compliance with GMP requirements for powder production
policies and achieved objectives.
● Analytical and problem-solving skills in handling operational issues
throughout the entire production process.
● Reviewed, assimilated, and summarized batch results and data to
provide recommendations for developing new process techniques and
improving product quality.

● Responsible for checking the calibration of all equipment and machines.

April 2004 — March 2009

Produc on specialist , CID Company (Ampoule-Sterile Area), Asyūţ
● Reasonable for preparation, filling, sterilization inspection&packaging of
all production steps.
● Conducted process validation for all ampule products at CID Company.
● Involved in toll manufacturing production of Tramadol ampoules for
October Pharma.
● Managed the production of Gallamine ampoules for Alexandria
Company and Vitamin B12 ampoules for Arabia Company.Vitamin B12
amp, Arabia company, AstraZeneca Company.
● Responsible for all production steps of Pulmicort and Rhinocerotic
inhalers.
● Implemented GMP requirements and policies in all production steps,
working towards achieving objectives.
 ● Achieved good quality and final yield for each batch, including those
from other companies.
● Successfully discussed and achieved good results during AstraZeneca
audits.
● Designed and updated the Batch Production Record (B.P.R) according to
new GMP requirements, parallel with the release and writing of
Standard Operating Procedures (S.O.P) for each production step.
● Managed and prepared raw materials for production, studying
production demands based on quarterly production programs
Excellent management of raw material storage and demand.
● Signed and released batches at the ampule and aerosol departments,
including all production steps, with high final batch yield.
● Managed and trained workers based on production needs.
● Responsible for choosing technical and price specifications for the W.F.I
Distiller from Italy (cor) and performed Installation Qualification (I.Q.)
and Operational Qualification (O.Q.) of the apparatus.
● Managed packaging materials.

Education

Very good, Faculty of Pharmacy Assuit University , Asyūţ 1999 — 2003 ·

Graduated with grade Very Good.

Courses

● Stability of pharmaceu cals ● Advanced G.M.P

course April 2005 — April 2005 Jan 2016

● Researches about modern ● HVAC system And

trends in drug delivery qualifica ons June 2018
technologies
June 2005 — June 2005 ● Water sta on And
qualifica ons Jul 2020
● Management &lead skills
course - April 2010 — April
2010