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トレンド企業

トレンド企業

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求人Amgen

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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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

Amgenについて

Amgen

Amgen

Public

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

10,001+

従業員数

Thousand Oaks

本社所在地

$138B

企業価値

レビュー

3.6

10件のレビュー

ワークライフバランス

3.2

報酬

4.1

企業文化

3.4

キャリア

2.8

経営陣

3.5

65%

友人に勧める

良い点

Excellent benefits and health benefits

Good pay and compensation

Supportive management and strong leadership

改善点

Limited career growth and promotion opportunities

Work-life balance challenges and long hours

Bureaucratic processes

給与レンジ

1,244件のデータ

Junior/L3

L2

L3

L4

L5

L6

Senior/L5

Director

Junior/L3 · Associate Fuel Operations

2件のレポート

$99,200

年収総額

基本給

$80,652

ストック

-

ボーナス

-

$99,200

$99,200

面接体験

5件の面接

難易度

3.0

/ 5

期間

14-28週間

内定率

40%

体験

ポジティブ 20%

普通 80%

ネガティブ 0%

面接プロセス

1

Application Review

2

HR Screen

3

Hiring Manager Interview

4

Technical/Role-Specific Interview

5

Panel Interview

6

Offer

よくある質問

Technical Knowledge

Behavioral/STAR

Past Experience

Data Analysis/Statistics

Culture Fit