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Quality Assurance Microsoft Office

Location:
Mansoura, Dakahlia Governorate, Egypt
Posted:
November 30, 2016

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Resume:

Curriculum Vitae

Walid Mohamed Abd Elgelil Saleh

Address: Baltim-Kafr el shikh– Egypt.

Mobile: +2 / 010********

Email: acxpb4@r.postjobfree.com

Objective

Seeking a challenging position in a reputable place where my academic background and interpersonal skills are well developed andutilized. Personal Information

Date of birth: October, 1st, 1983

Nationality: Egyptian

Marital Status: Married

Military Service: Exempted

Educational Qualifications

Degree: Bachelor of pharmaceutical science and clinical pharmacy. University: 6 October University – Egypt

Grade: Good

Date of Graduation: July 2005.

Training :

1-attended GMP training in Biomedical pharmaceutical industries. 2-attended self inspection training in Biomedical pharmaceutical industries.

3-attended marketing training in Panax pharma

Experience

Biomedical pharmaceutical industries from January 2015 until now

Quality assurance supervisor :

1- Ensure compliance with GMP.

2- Batch release of finished products.

3- Reviewing and approving of quality documentation including validation protocols and reports, change controls and GMP deviations

4- Writing and approving standard operating procedures 5- Involvement with customer complaints and product investigations

6- Responding to complaints in a timely manner

7- Participating in self inspections and regulatory inspections 8-Ensuring safe working practice

9- Ensuring good relations and communications with all team members

10- Working with all members of staff to maintain and develop the positive progressive culture

11- Observing and complying with cGMP

12- Observing and complying with company health and safety policies

13- Observing and complying with company SOPs

14- Undertaking any other duties which may be requested by line manager, for which training and/or an explanation has been provided and understood

15- Suppliers evaluation and approval

16- Periodic GMP training for relevant staff.

Biomedical pharmaceutical industries from July 2011- December 2014

Quality assurance specialist :

1- handling of product complaints

2- development, periodic review, revision and implementation of SOPs as required

3- annual product reviews and review of stability reports for compliance with Egyptian guidelines

4- QA annual self-inspection and quality agreements with manufacturers, and distributors

5- conducting inspections of distributors and suppliers as necessary per GMP requirements

6- acting as primary quality contact person with Third Party Logistics (3PL) and as qualified person for internal quality compliance matters

7- implementing recall procedures if necessary

8- monitoring QA aspects of warehousing practices for compliance with warehouse procedure manuals (Third Party Logistics-3PL). 9- liaising with customers and regulatory authorities regarding quality matters, including hosting inspections and responding to observations.

10- periodic GMP training for relevant staff

11- Participate in personal development and training sessions. 12- Timely approval of incoming batches, batch inspection and release according to company SOPs

13- Handling deviations

14- Maintaining retained samples according to GMP

Sabaa international company for pharmaceutical and chemical industry from November 2010-june 2011

IPC specialist:

1- sampling of intermediate product and finished product 2- performing IPC tests for solid dosage forms including weight variation, disintegration time, dissolution time and rate, and measuring pH of solutions

3- sampling of raw materials and primary packaging materials From 2007 - 2010:

Worked as a pharmacist in several pharmacies in Baltim and Hamoul

From 2006 - 2007:

Worked as full time medical rep. in Panax pharma

Computer skills:

1- Windows XP, Windows 7

2- Microsoft office (word- excel- powerpoint)

3-Very good internet user

Practical Skills:

1- IPC of solid dosage forms.

2- Writing and approving BPR.

3- Sampling of raw materials, packaging materials and finished products.

4- Good knowledge in cGMP .

5-Self inspection.

6- Quality system.

7- Writing and investigating NCRs, and CAPAs.

PERSONAL QUALITIES

1- Good communication skills (verbal and written). 2- Ability to assume responsibility and act on own initiative. 3-Good self management, organisational and planning skills. 4-Ability to adhere to strict deadlines.

5- Excellent reasoning skills.

6- Hands-on approach with a ‘can-do’ attitude.

7- Good listener, but proactive in group discussions. 8-Good team player.

9- Detail oriented person

10- Solid decision making skills.

11- Ready to move in if it is necessary for work

Languages skill:

1- Arabic: Mother tongue

2- English:Very good Writer and Speaker.

Last update in November 2016



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