Senior Quality Manager - Pharma (m / w / d) 100%

nemensis ag; Basel; Hybrid; CHF 80’000 - 100’000; Vollzeit

Zusammenfassung

A leading global pharmaceutical company is seeking a Quality Lead in Basel, Switzerland, to oversee quality assurance in drug development. The ideal candidate will have significant experience in quality operations and regulatory standards, leading interdisciplinary teams and ensuring compliance with health authority requirements. This fixed-term contract position offers flexibility with two days of home office and a competitive hourly salary. Join a dynamic environment and elevate your quality career with a strong network in Life Sciences.

Leistungen

Comprehensive support throughout application process

Access to a broad client network

Qualifikationen

• 10+ years of pharmaceutical quality/operations experience or Master's with 5+ years relevant experience.
• Deep knowledge of quality standards in drug substance, drug product, and medical devices.
• Strong leadership in managing interdisciplinary teams and projects.

Aufgaben

• Lead complex quality projects within global pharmaceutical development teams.
• Provide strategic quality oversight for development projects.
• Guide PAI and submission preparations, ensuring inspection readiness.

Kenntnisse

Leadership

Quality assurance

Regulatory standards

Drug development

Interdisciplinary team management

Fluency in English

Ausbildung

Bachelor's degree or Master's in relevant field

Jobbeschreibung

Shape the future of pharmaceutical excellence as a Quality Lead (m / w / d).

Position Details

• Duration: 01.09.2025 to 30.09.2026 (1 year extension possible)
• Location: Basel, Switzerland (2 days Home Office)
• Position Type: Temporary
• Salary: CHF 50,- / h - 90,- / h
• Personal computing equipment required

About Our Client

Our client is a leading global pharmaceutical company based in Basel, specializing in innovative research and development across therapeutic areas such as oncology, immunology, cardiovascular medicine, and neuroscience. Operating in over 155 countries, they are committed to transforming medicine through science and digital technologies.

Your Responsibilities

• Lead complex quality projects within global pharmaceutical development teams.
• Provide strategic quality oversight for development projects with scientific and technical expertise.
• Represent quality assurance at expert panels and global quality board meetings.
• Guide PAI and submission preparations, ensuring inspection site readiness.
• Develop project strategies aligning with regulatory requirements.
• Support due diligence activities by assessing potential in-licensing products.
• Manage quality aspects of medical device and drug-device combination products.
• Coach and mentor team members and participate in recruitment.

Your Profile

• Bachelor's degree with 10+ years of pharmaceutical quality/operations experience or Master's with 5+ years relevant experience.
• Deep knowledge of quality standards in drug substance, drug product, and medical devices.
• Experience with health authority inspections (FDA, EMA) and regulatory submissions.
• Strong leadership in managing interdisciplinary teams and projects.
• Expertise in drug development, quality assurance, and control.
• Fluent in English; local language skills are a plus.
• Strategic thinker with quality awareness in matrix environments.

Benefits with nemensis

• Specialized personnel consulting in Life Sciences based in Basel.
• Comprehensive support throughout the application process.
• Access to a broad client network and exciting positions in Northwestern Switzerland.
• Fast and straightforward entry with personalized guidance.

Ready to elevate your quality career in a dynamic pharmaceutical environment? Contact nemensis AG — we've helped thousands find their ideal job and grow professionally. What can we do for you today?

Industry: Pharma Industry

Function: Quality Assurance

Employment Type: Fixed-term Contract