ELSAYED NEGM

Production specialist

Nationality : Egyptian

Country of Birth: Egypt

City of Birth : Alexandria

Date of Birth : 30/11/1969

Phone number : +201*********

Address : ** ******* *** **. Alexandria,Egypt

Email : ac163p@r.postjobfree.com

Education

1987-1989

Abasia Hight School

Alexandria – Egypt

1989-1992

Faculty of agriculture

Alexandria – Egypt

Language skills

Arabic

English [fluent in speech, writing and reading ]

Work experience

1993-2016

-Amriya pharmaceutical Ind.

-Evaluate and approve reports and protocols.

-Ensure cGMP and CFR compliance of operating areas.

-Revise, update, and review procedures.

-Manage the development and revision of SOPs.

-Evaluate current operating procedures and recommend changes to management to optimize production.

-Responsible for selection, training, evaluation, staff relations and development of staff.

- Collaborate with cross-functional teams in completing production activities.

-Assist in developing and maintaining department goals.

-Ensure maintenance and re-validation of systems in completing production activities.

-Develop, implement and assess solutions for complex problems.

-Monitor and follow up all kind of packing machines such as filling, powder, blister, Ink-jet, stretch banding, shrink machines.

Professional training and courses

-New Topical Dosage forms.

-Clean room technology, hygiene and sanitation.

-GMP Inspection.

-Change control.

-GMP in production personnel.

-Investigation out of specification result.

-Validation in pharmaceutical End.

-Validates and equipment qualification.

-Recent trends in process validation.

-New Topical Dosage forms.

-ISO 9000, 9001, 9002, 9003.

-ISO 2001/2002.

-ISO 14000, 14001.

-Pharmaceutical water system/ water analysis.

-Basic data information in CGMP.

-Business communication.

-Documentation and Documentation inspection cleaning validation.

-Corrective and preventive action.

-Risk analysis.

-Occupational safety and health.

-Emergency and evacuation plan.

-Positive behaviors in the work community.

-Good storage practice [GSP].

-Preparation of reports and the successful use of statistical methods in their preparation.

-Maintain work environments.

-The common technical Document [CTD] for European submissions.

-Change control.

-Drug targeting.

-Process validation.

-Reports.

-Good manufacturing practice (G.M.P).

-Good Storage practice (G.S.P).

-GMP Inspection approach of pharmaceutical facilities.

-Recent trends in process validation.

Contact this candidate