採用
必須スキル
GCP
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 https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Non-Employee
Job Category:
Non-Standard
All Job Posting Locations:
Beijing, China, CN027 Shanghai Gui Qing Rd
Job Description:
POSITION SUMMARY:
This Specialist/Sr. Specialist, APAC Inspection Management is responsible for ensuring end-to-end (E2E) management of inspection management-related systems per company’s requirements (e.g., contents & timeline), including but not limited to: CURVE (proper maintenance of inspection information and data); D2 (archive of inspection related information and data); Inspection related Share Point sites etc.
This position is also responsible for supporting the Core Inspection Team Lead to manage Health Authorities inspections in the non-GMP spaces in the APAC region. To extract, analyse (under supervision if needed), and present general & specific information/data (metrics) on inspections. To support activities in monitoring regulatory intelligence focusing on the APAC region and provide support as needed the RDQ Regulatory Intelligence function, e.g., translation of regulations, requirements etc.
PRINCIPAL RESPONSIBILITIES:
- Responsible for ensuring end-to-end (E2E) management of inspection management-related systems per company’s requirements (e.g., contents & timeline), including but not limited to: CURVE (proper maintenance of inspection information and data); D2 (archive of inspection related information and data); Inspection related Share Point sites etc.
- Responsible for supporting the coordination of inspection preparation, conduct and post-inspection activities for APAC in the GLP, GCP and PV areas.
- Responsible for extracting, analyzing (under supervision if needed), and presenting general & specific information/data (metrics) on inspections.
- Responsible for supporting activities in monitoring regulatory intelligence focusing on the APAC region and providing support as needed the RDQ Regulatory Intelligence function, e.g., translation of regulations, requirements etc.
- Responsible for supporting CIT Lead to monitor (mining) of external industry and internal J&J inspection outcomes and trends, ensuring this information is proactively shared within R&D Business partners and effectively used to shape the audit and inspection readiness programs.
- Responsible for supporting other activities within APAC inspection team, as needed.
- Responsible for ensuring timely submission of inspection-related information into company databases (e.g., CURVE, D2, COMET, etc.).
DECISION-MAKING AND PROBLEM SOLVING:
- Support manager to resolve strategic business/regulatory issues with franchise, corporate and business group leaders. Global spokesperson and negotiator with Regulatory Authorities.
INDEPENDENCE/AUTONOMY:
- Operates with minimal guidance from supervisor.
- Expected to lead and be proactive in the setting of priorities to achieve R&D Quality goals and objectives.
REPORTING RELATIONSHIPS:
- Reports directly to the Associate Director, APAC Inspection Management
WORKING RELATIONSHIPS/INTERFACES:
- Works very closely with other R&D Quality functions to ensure the inspection readiness.
- Interacts with quality professionals within R&D Quality and at other J&J companies.
- Interacts as appropriate with functional professionals as needed.
KNOWLEDGE, EDUCATION, EXPERIENCE, COMMUNICATION SKILL REQUIREMENTS:
- Requires at least 2-5 years of experience in a quality function working on complex and significant compliance topics. Have comprehensive knowledge of worldwide GCP, GLP, PV, IT & other applicable compliance regulations.
- Demonstrated effective influencing, interpersonal, written and verbal communications skills as well as a proven track record of sustaining compliance in complex organizations. Regulatory Authority experience is desirable.
- BS required. Masters in related field, advanced degree advantages.
RELATED EXPERIENCE:
- Experience with Regulatory Authorities is a significant asset.
総閲覧数
0
応募クリック数
0
模擬応募者数
0
スクラップ
0
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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
4.0
10件のレビュー
ワークライフバランス
3.8
報酬
4.2
企業文化
4.1
キャリア
3.5
経営陣
4.3
75%
友人に勧める
良い点
Supportive and approachable management
Excellent benefits and compensation
Flexible work arrangements and work-life balance
改善点
High-pressure and demanding work environment
Slow bureaucratic processes
Heavy workload and high 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
7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
Pre-recorded/Video Interview
4
Technical/Panel Interview
5
Final Interview
6
Offer
よくある質問
Behavioral/STAR
Technical Knowledge
Past Experience
Culture Fit
ニュース&話題
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·
2d ago