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IMP Quality Clinical Packaging Manager - Job Opportunity at Randstad

Kaiseraugst, Switzerland
Full-time
Mid-level
Posted: May 20, 2025
Hybrid
CHF 110,000 - 140,000 per year based on Swiss pharmaceutical industry standards and role responsibilities

Benefits

Flexible remote work policy (20% remote allowed)
Standard working hours supporting work-life balance
Professional development in GMP environment
Modern workplace with NewWork principles

Key Responsibilities

Lead quality oversight for clinical packaging operations with direct impact on patient safety and trial success
Execute lot disposition and certification as Swiss Responsible Person delegate
Drive continuous improvement initiatives across IMP quality operations
Manage GMP compliance and quality standards for clinical trial materials
Develop and implement quality control procedures and documentation
Partner with cross-functional teams to ensure operational excellence

Requirements

Education

Master Degree in Life Sciences or Engineering or similar degree

Experience

Minimum 3 years in pharmaceutical industry quality manager role

Required Skills

cGMP knowledge Clinical development phase quality requirements German and English fluency SAP and Veeva experience (preferred) Strong communication abilities Problem-solving capabilities Self-motivation Team leadership Change management
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Sauge AI Market Intelligence

Industry Trends

Clinical trial complexity is increasing with more personalized medicine approaches, requiring sophisticated quality management systems Regulatory requirements for IMPs are becoming more stringent globally, particularly in emerging markets Digital transformation in quality management systems is driving demand for expertise in electronic quality management systems

Role Significance

Part of a 12-person team, typical for specialized quality operations in major pharmaceutical organizations
Mid to senior-level position with significant responsibility as delegate of Swiss Responsible Person for IMPs

Key Projects

Implementation of new quality management systems Clinical trial material certification programs Process optimization initiatives Regulatory compliance projects Quality system harmonization efforts

Success Factors

Deep understanding of GMP requirements and their practical application Strong stakeholder management abilities across multiple departments Ability to balance quality requirements with operational efficiency Change management expertise in regulated environments

Market Demand

High demand due to increasing clinical trial activities and stringent regulatory requirements in Switzerland's pharmaceutical sector

Important Skills

Critical Skills

GMP expertise is fundamental for ensuring compliance and product quality Communication skills are essential for cross-functional collaboration Change management capabilities are crucial for process improvement initiatives

Beneficial Skills

Digital system expertise (SAP, Veeva) enhances efficiency Project management skills support process improvement initiatives Industry network can facilitate best practice sharing

Unique Aspects

Combination of traditional GMP responsibility with modern organizational transformation
Significant autonomy in quality decisions while maintaining compliance
Opportunity to influence global clinical trial quality standards

Career Growth

2-3 years in role before advancement opportunity, depending on performance and organizational growth

Potential Next Roles

Senior Quality Manager Head of Quality Operations Quality Director Regulatory Affairs Director

Company Overview

Randstad

Major pharmaceutical company with significant presence in clinical research and development

Leading position in pharmaceutical development with substantial investment in clinical trials
Strategic location in Switzerland's pharmaceutical hub with global reach
Progressive work environment embracing NewWork principles and agile methodologies
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