18 beste Stellen als associate program – aktuell auf Personalsuche

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Applied Physicist - n_TOF Facility (SY-STI-BMP-2026-103-GRAP)
CERN —Genf, GE
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Senior Director, European Sales (m/f/d)
Molecular Devices —Kloten, ZH
- 100%
- Homeoffice
- Oracle
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- Bachelor
- Bezahlte Ferien
Senior Associate - Supply Chain Cyber Security Specialist (Cyber Risk Advisory)
PwC —Zürich, ZH
- 100%
- Englisch
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Business Developer - French Speaking
Ebury —Zürich (Kreis 7), ZH
- Microsoft Excel
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Senior Associate / Manager Financial Services Consulting - Liquidity & Funding
PwC —Zürich, ZH
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- Microsoft Powerpoint
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Safety and Controls Engineer for the CMS Experiment (EP-CMS-EC-2026-119-LD)
CERN —Genf, GE
- 100%
- Englisch
- Forschungserfahrung
- Master
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Channel Sales Engineer - DACH
Cyera —Genf, GE
- 100%
- Homeoffice
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Retail Sales Associate (part-time)
Canada Goose EU B.V., Amsterdam, Zweigniederlassung Zug —Zürich, ZH
- Teilzeit
- Microsoft Word
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Associate technical program manager
Swiss Biotech Association —Basel, BS
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da Vinci Clinical Territory Associate (m/w/d)
Intuitive Surgical —Zürich, ZH
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- Englisch
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Senior Manager – Pricing & Value Optimization (EMEA)
BD —Eysins, VD
- Englisch
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Associate Director, International Auditing

Biogen -
Baar, ZG

Jetzt bewerben

Details zur Stelle

100% | Pensum: 90-100%
vor 23 Stunden

Qualifikationen

Management-Erfahrung
Doktorat
Rechnungsprüfung
Englisch
Qualitätssicherung
Bachelor
Produktion
Führungserfahrung
ISO 13485

Vollständige Stellenbeschreibung

About This Role:

As the Associate Director of International Auditing, you will spearhead the planning, execution, and oversight of Quality audits across manufacturing sites, affiliates, contract manufacturers, suppliers, and service providers throughout Europe and the Rest of World (RoW). Situated in Baar, Switzerland, this role is pivotal in ensuring our audit program is robust, risk-based, and aligned with global quality standards to uphold regulatory compliance, patient safety, and product quality. Reporting to the Director of Quality Risk, Auditing and Governance, you will lead a team of auditors, fostering collaboration with global Quality functions to ensure audit outcomes drive effective risk mitigation and continuous improvement. Your leadership will enhance our Quality Management System and contribute to the organization's overall success.

This role requires approximately 25% international travel across Europe and RoW to support on-site audits, stakeholder engagement, and regulatory activities.

What You’ll Do:

Lead the planning and execution of a risk-based audit program for internal manufacturing sites, affiliates, CMOs, suppliers, and service providers across Europe and RoW.
Ensure audits are conducted in accordance with global Quality policies, regulatory requirements, and industry standards.
Oversee audit execution, including scope definition, auditor assignment, on-site/remote activities, and reporting.
Review and approve audit reports for quality, consistency, and accuracy.
Ensure timely and effective response to audit observations, including corrective and preventive actions (CAPAs).
Lead and develop a regional audit team of 4–7 direct reports, setting performance goals and providing coaching.
Serve as the primary Quality audit point of contact for European and RoW stakeholders.
Drive continuous improvement of audit processes, tools, and metrics.
Support regulatory inspections and due diligence activities as required.
Collaborate with stakeholders to drive remediation and continuous improvement.

Who You Are: You are a strategic thinker with a passion for quality assurance and auditing. You possess strong leadership skills, enabling you to guide a team effectively and foster collaboration across various functions. Your ability to communicate clearly and manage complex situations allows you to drive audit excellence and compliance. You thrive in an international setting and are committed to maintaining high standards of product quality and patient safety.

Required Skills:

Bachelor’s Degree in Science, Engineering, Pharmacy, or related discipline required; advanced degree preferred or equivalent combination of education and experience.
12–15 years of experience in Quality Assurance and GxP auditing within the pharmaceutical or biotechnology industry.
Minimum 5 years of people management experience and demonstrated leadership of complex, international audit programs.
Experience auditing manufacturing sites, CMOs, suppliers, and service providers in global regulatory environments.
Proficiency in English.

Preferred Skills:

Advanced terminal degree (MD, PhD, PharmD).

Job Level: Management

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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Erweiterte Suche

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