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Regulatory Affairs Specialist | Johnson & Johnson MedTech | Riyadh - KSA
Riyadh, Saudi Arabia
·
On-site
·
Full-time
·
6d ago
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Regulatory Affairs Group:
Job Sub Function:
Regulatory Product Submissions and Registration:
Job Category:
Professional
All Job Posting Locations:
Riyadh, Saudi Arabia
Job Description: About Med Tech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Regulatory Affairs Specialist.
Purpose:
The main task of a Regulatory Affairs specialist in Johnson & Johnson is Launching of Medical Device Products in Saudi Arabia Market in compliance with the Regulatory registration & importation guidance.
You will be responsible for:
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Preparing, compiling and submission of registration/ re-registration products files in addition to variation submission on time directly in Saudi Arabia or through J&J distributors when applicable
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SFDA meetings.
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Clearance support to distributers.
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Updating the regulatory tracking systems
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Having the renewed certificates & re-registration licenses of expired ones on time.
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Responding to Change Impact Assessments before due dates.
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Doing Copy Review process for promotional materials on time upon request.
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Lift all regulatory restrictions for products that can be shipped to Saudi Arabia
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Tender support to commercial teams & distributers
Qualifications / Requirements:
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Education: Bachelor’s (B.Sc.) Degree of Biomedical engineering or Sciences
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Experience; min. 2 years
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Language: English
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Arabic
Key Competencies:
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Time Management
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Presentation & Communication Skills
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Involvement in Regional Projects.
Required Skills: Preferred Skills:
Analytical Reasoning, Brand Research, Business Behavior, Design Thinking, Detail-Oriented, Execution Focus, Market Research, Package and Labeling Regulations, Process Oriented, Product Licensing, Product Packaging Design, Project Management, Proof Reading Software, Quality Assurance (QA), Regulatory Affairs Management, Regulatory Compliance, Safety-Oriented
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模擬応募者数
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スクラップ
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Johnson & Johnsonについて

Johnson & Johnson
PublicJohnson & Johnson (J&J) is an American multinational pharmaceutical, biotechnology, and medical technologies corporation headquartered in New Brunswick, New Jersey, and publicly traded on the New York Stock Exchange.
10,001+
従業員数
New Brunswick
本社所在地
$400B
企業価値
レビュー
3.3
2件のレビュー
ワークライフバランス
4.0
報酬
2.5
企業文化
2.5
キャリア
2.0
経営陣
2.0
65%
友人に勧める
良い点
Good work-life balance
Strong R&D environment
Potential for fulfilling work
改善点
Significant pay cuts
Employees feel unimportant
Unclear role expectations
給与レンジ
2,250件のデータ
Mid/L4
Senior/L5
Director
Mid/L4 · Manager
338件のレポート
$155,591
年収総額
基本給
$137,488
ストック
-
ボーナス
$18,103
$106,549
$229,934
面接体験
6件の面接
難易度
3.0
/ 5
期間
14-28週間
面接プロセス
1
Application Review
2
HR Screen
3
Personality/Assessment Test
4
Virtual/Video Interview
5
Hiring Manager Interview
6
Offer
よくある質問
Behavioral/STAR
Technical Knowledge
Culture Fit
Past Experience
ニュース&話題
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News
·
1d ago
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News
·
1d ago
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News
·
2d ago
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News
·
2d ago