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채용Amgen

Manager Quality – International & Distribution Quality (IDQ)

Amgen

Manager Quality – International & Distribution Quality (IDQ)

Amgen

Netherlands - Breda

·

On-site

·

Full-time

·

3d ago

Career Category

Quality

Job Description

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us as:

Manager Quality – International & Distribution Quality (IDQ)

At Amgen Breda medicines are labelled, assembled, stored and eventually shipped to various countries worldwide. Every day more than 1000 people with 42 different nationalities are working on supply chain processes, manufacturing, marketing and sales of our medicines and clinical research into new medicines.

Live What you will do

The International & Distribution Quality (IDQ) team is looking for an experienced Quality Manager to support a diverse portfolio of regional activities across Europe.

In this vital role, you will provide Quality leadership and oversight across IDQ operations, ensuring compliant distribution of pharmaceutical products in line with Good Distribution Practices (GDP) across the EMEA region.

Let’s do this. Let’s change the world.

In this vital role you will:

  • Provide Quality oversight for storage, transportation and distribution activities, ensuring compliance with GDP, GMP and applicable pharmaceutical regulations
  • Oversee and continuously improve the Quality Management System (QMS) for IDQ operations
  • Act as Responsible Person (RP) or RP Back‑up, maintaining full regulatory compliance and reporting quality matters to senior management
  • Review, manage and approve Quality records including Deviations, CAPAs, CAPA EVs, Change Controls and Continuous Improvement initiatives
  • Support and participate in audits, self‑inspections and Health Authority inspections
  • Act as owner or Quality contact for deviation and CAPA records within Quality and Supply Chain
  • Track and ensure timely completion of Quality‑owned records
  • Provide Quality review and approval of controlled documents owned by Supply Chain
  • Assess and support planned changes, including product launches and record retirement, partnering closely with Country Responsible Persons to ensure regulatory compliance
  • Provide Quality oversight and ownership of continuous improvement programs and strategic projects within Quality and Supply Chain
  • Identify, escalate and communicate quality, compliance, supply and safety risks to senior management and support recall activities where required
  • Deliver training, awareness sessions and guidance to Quality and Supply Chain stakeholders to promote procedural compliance and quality culture
  • Work collaboratively and cross‑functionally with internal and external stakeholders, ensuring pharmaceutical products are distributed safely, compliantly and to the highest quality standards.

Win What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek brings:

  • In‑depth knowledge of European Pharmaceutical legislation, including:
  • Good Distribution Practice (GDP)
  • Good Manufacturing Practice (GMP)
  • Falsified Medicines Directive
  • Role of the European Medicines Agency (EMA) and Country Health Authorities
  • Life Sciences degree or related discipline
  • Relevant experience in Quality and/or Supply Chain within a regulated pharmaceutical environment
  • Fluency in English
  • Strong organizational skills with the ability to multitask and prioritize effectively
  • High attention to detail and accuracy
  • Experience working with Quality Management Systems (QMS), ERP systems and Microsoft Office
  • Confidence working in a complex, matrixed and international environment

Thrive What you can expect of us

As we work to develop treatments that take care of others, we work to care for our teammates’ professional and personal growth and well-being. Therefore, Amgen is regularly recognized as a Best Place To Work ©.

  • Vast opportunities to learn and move up and across our global organization.
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.
  • Generous Total Rewards Plan comprising competitive salary, bonus structure, fixed 13th month, holiday allowance and collective health insurance.
  • Focus on vitality with an on-site gym, vitality program and a restaurant with healthy food.

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총 조회수

0

총 지원 클릭 수

0

모의 지원자 수

0

스크랩

0

Amgen 소개

Amgen

Amgen

Public

A biotechnology company that develops and manufactures human therapeutics for various illnesses and diseases.

10,001+

직원 수

Thousand Oaks

본사 위치

$138B

기업 가치

리뷰

3.6

10개 리뷰

워라밸

3.2

보상

4.1

문화

3.4

커리어

2.8

경영진

3.5

65%

친구에게 추천

장점

Excellent benefits and health benefits

Good pay and compensation

Supportive management and strong leadership

단점

Limited career growth and promotion opportunities

Work-life balance challenges and long hours

Bureaucratic processes

연봉 정보

1,244개 데이터

Junior/L3

L2

L3

L4

L5

L6

Senior/L5

Director

Junior/L3 · Associate Fuel Operations

2개 리포트

$99,200

총 연봉

기본급

$80,652

주식

-

보너스

-

$99,200

$99,200

면접 경험

5개 면접

난이도

3.0

/ 5

소요 기간

14-28주

합격률

40%

경험

긍정 20%

보통 80%

부정 0%

면접 과정

1

Application Review

2

HR Screen

3

Hiring Manager Interview

4

Technical/Role-Specific Interview

5

Panel Interview

6

Offer

자주 나오는 질문

Technical Knowledge

Behavioral/STAR

Past Experience

Data Analysis/Statistics

Culture Fit