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Nadia Issad, Assistant Manager Regulatory Affairs

Nadia Issad

Assistant Manager Regulatory Affairs·Gulf Pharmaceutical Industries (Julphar)

United Arab Emirates

Bachelor's degree, Biochemistry

Work experience

Total years of experience: 23 years, 5 months

Assistant Manager Regulatory Affairs

May 2012 - Present

Gulf Pharmaceutical Industries (Julphar)

Ras Al Khaimah, United Arab Emirates

May 2012 - Present

More than 8 years of experience in MEA pharmaceutical industries between regulatory affairs and business development, quality control, quality assurance and supply chain, acquiring various experiences in marketing, sales, and medical affairs field.
I aim at maximizing my experience and potential by taking more challenging roles & responsibilities in Regulatory Affairs, Business development, Quality and Government affairs as well as in Sales & Marketing field.

Company industry:
Pharmaceutical Manufacturing
Job role:
Medical, Healthcare, and Nursing

Patient Relation Officer

January 2010 - May 2012

Al Zahra Private Hospital

United Arab Emirates

January 2010 - May 2012

Al Zahra Private Hospital January 2010 - May 2012
One of the largest private hospitals in the UAE

Patient Relation Officer
• Coordinating between different departments to ensure proper communication and reporting practices.
• Handling and solving patients' complaints including insurance approvals.
• Ensuring that all procedures are carried out in accordance with the current policy.
• Maintaining strong relationships with the healthcare providers.

Company industry:
Other Healthcare Services
Job role:
Customer Service and Call Center

Regulatory and Quality Control Manager

September 2003 - December 2009

Laboratoire Pharmaghreb

Algiers, Algeria

September 2003 - December 2009

Laboratoire Pharmaghreb September 2003 - September 2009
One of the pioneer Pharmaceutical Industries in Algeria

Regulatory and Quality Control Manager
• Responsible for new regulatory planning, new product submission, approval, pricing and local packaging
development.
• Interacting with regulatory partners (internal & external)
• Preparing dossier and ensuring timely product registration/ launch.
• Providing technical data &/or solutions required by local forecast & logistics.
• Maintaining the Good Manufacturing Process.
• Involved in different stages of product development.
• Supervising the internal audit.
• Managing the supply chain and raw material purchase.

Company industry:
Pharmaceutical Manufacturing
Job role:
Quality Control

Senior Auditor

June 2009 - September 2009

Algerac - Organisme Algerien

Algiers, Algeria

June 2009 - September 2009

Algerac - Organisme Algerien d'Accreditation June 2009 - September 2009
Official Accreditation Body in Algeria

• Auditor in ALGERAC: EN, NF, ISO CEI 17025

Company industry:
Management Consulting
Job role:
Medical, Healthcare, and Nursing

QC Assistant Manger

March 2003 - September 2003

Castel Group

March 2003 - September 2003

Castel Group March 2003 - September 2003
Manufacturing of Soft Drinks ALGERIA

• QC Assistant Manger
Mobile: 00971 50 597 2571 Email: issadnadiadz@yahoo.fr
nadiaissad1110@gmail.com
TRAININGs, CERTIFICATES AND AWARDS RECEIVED

Company industry:
Industrial Production
Job role:
Other

Assistant Manager quality Control

January 2003 - September 2003

Castel group SBOA

Oran, Algeria

January 2003 - September 2003

Company industry:
Other Healthcare Services
Job role:
Quality Control

Regulatory Affairs Assistant Manager

-

The Gulf

-

The Gulf leading pharmaceutical company with turnover of 1.36 billion AED in 2013

Regulatory Affairs Assistant Manager
Responsible for regulatory activities across Africa regions. In addition to be highly involved in business
development, project management and marketing. My main job responsibilities include: • Planning long term objectives for new products registration & launch and updating the marketing & sales about approvals & pricing.
• Providing Regulatory Affairs intelligence by informing local management with current & changing
regulations.
• Building & maintaining strong business relationship with the external Health Authorities, industry
organizations, distributers & KOLs.
• Preparing registration dossiers as per countries' requirements, ensuring dossiers submission, following up with authorities on approvals and fulfilling additional authority requirements.
• Maintaining existing products in terms of renewals, variations, labeling, etc.
• Preparing and reviewing labeling, pack leaflets, Summary of Product Characteristics (SPC) and ensuring
compliance with the external legislations.
• Handling Pharmacovigilance & product complaints.
• Pricing and reimbursement
• Working closely with manufacturing sites in Algeria & Tunisia, to ensure the comprehensiveness of each
country's requirements, thus ensuring timely submission & registration as planned.
• Highly involved in the evaluation and management of the company projects with partners across North
Africa region.
• Preparing and validating all Marketing activities and promotional materials
• Presenting the corporate profile internally and externally.
Mobile: 00971 50 597 2571 Email: issadnadiadz@yahoo.fr
nadiaissad1110@gmail.com

Company industry:
Banking
Job role:
Medical, Healthcare, and Nursing

Education

University of Oran

January 2003

January 2003

Bachelor's degree, Biochemistry

• 2003: Bachelor degree in Biochemistry, from University of Oran - ALGERIA

January 1997

January 1997

High school or equivalent, natural sciences

• 1997: High School (Baccalaureate) in natural sciences.

Skills

Marketing
Expert
Marketing
Expert
Quality Assurance
Expert
Quality Assurance
Expert
Project Management
Expert
Project Management
Expert
Market Access
Expert
Market Access
Expert
Regulatory Affairs
Expert
Regulatory Affairs
Expert
AUDIT
AUDIT
BSEE/SUPPLY
BSEE/SUPPLY
INTERNAL AUDIT
INTERNAL AUDIT
LOGISTICS
LOGISTICS
MANUFACTURING PROCESS
MANUFACTURING PROCESS
PACKAGING
PACKAGING
PRICING
PRICING
PRODUCT DEVELOPMENT
PRODUCT DEVELOPMENT
SOLUTIONS
SOLUTIONS
SUPPLY CHAIN
SUPPLY CHAIN
Marketing
Expert
Marketing
Expert
Quality Assurance
Expert
Quality Assurance
Expert
Project Management
Expert
Project Management
Expert
Market Access
Expert
Market Access
Expert
Regulatory Affairs
Expert
Regulatory Affairs
Expert

Languages

Arabic
Expert
English
Expert
French
Expert

Training and Certifications

Training
Pharmaceutical Regulatory Affairs in Africa (London).
Forum management/CPD Certification
Apr 2014
Standard EN, NF, ISO CEI 17025 .(Algeria).
AFNOR FRANCE
Jul 2009
USP Quality Standard for Medicines (UAE).
USP Quality Standard for Medicines. USA
Feb 2013
Preparation and Publication of Product Dossier in NeeS/ eCTD Format (UAE)
NeeS/ eCTD
Dec 2012
Effective Communication Skills and Presentation Styles (UAE).
Julphar Training Center UAE
Jul 2012
Winner Presentation Management
Julphar training Center
Jul 2012
Best Administrative Practices in Pharmacy (UAE)
RAKCOPS
Jan 2013
Enhancing Customer Cares (UAE).
Customer Cares (UAE).
Mar 2010