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트렌딩 기업

트렌딩 기업

채용

채용Johnson & Johnson

Senior Specialist, APAC Inspection Management (Contractor)

Johnson & Johnson

Senior Specialist, APAC Inspection Management (Contractor)

Johnson & Johnson

2 Locations

·

On-site

·

Full-time

·

1mo ago

필수 스킬

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.

총 조회수

0

총 지원 클릭 수

0

모의 지원자 수

0

스크랩

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Johnson & Johnson 소개

Johnson & Johnson

Johnson & 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+

직원 수

New Brunswick

본사 위치

$400B

기업 가치

리뷰

4.0

10개 리뷰

워라밸

3.8

보상

4.2

문화

4.1

커리어

3.5

경영진

4.3

75%

친구에게 추천

장점

Supportive and approachable management

Excellent benefits and compensation

Flexible work arrangements and work-life balance

단점

High-pressure and demanding work environment

Slow bureaucratic processes

Heavy workload and high expectations

연봉 정보

2,250개 데이터

Mid/L4

Senior/L5

Director

Mid/L4 · Manager

338개 리포트

$155,591

총 연봉

기본급

$137,488

주식

-

보너스

$18,103

$106,549

$229,934

면접 경험

7개 면접

난이도

3.0

/ 5

소요 기간

14-28주

면접 과정

1

Application Review

2

HR Screen

3

Pre-recorded/Video Interview

4

Technical/Panel Interview

5

Final Interview

6

Offer

자주 나오는 질문

Behavioral/STAR

Technical Knowledge

Past Experience

Culture Fit