Vice President, Quality and Regulatory Compliance

Clinilabs; Basel; Hybrid; CHF 250.000 - 380.000; Vollzeit

Zusammenfassung

Clinilabs seeks a Vice President of Quality Assurance to lead the quality and regulatory teams, shaping strategy for quality systems and compliant operations across clinical trials. You will ensure cGCP adherence, regulatory readiness, and harmonization of processes within the organization.

This role requires deep GXP experience, strong leadership, and the ability to mentor staff while engaging with FDA, MHRA, and other regulators to drive compliant outcomes.

Qualifikationen

• Bachelor’s degree required; advanced degrees preferred.
• Minimum 15 years in a GXP function.
• At least 10 years in a leadership role in quality/compliance.
• Proven experience with FDA/MHRA inspections and responses.
• Strong influencing and cross-functional leadership abilities.
• Experience leading regulatory inspections without direct line authority.
• Ability to manage complex, diverse teams in regulated industry.
• Excellent written and oral communication and collaboration skills.
• Cross-cultural communication experience required.
• Prior experience driving performance results.

Aufgaben

• Provide leadership to growing quality and regulatory department.
• Develop strategy and maintain Clinilabs Quality Systems.
• Interact with regulatory bodies such as FDA/MHRA.
• Oversee internal and external audits.
• Develop and monitor vendor qualification programs.
• Mentor staff to prepare for higher responsibilities.
• Lead process and system strategy decisions for harmonization.
• Ensure regulatory compliance of clinical activities.

Kenntnisse

Leadership

Regulatory expertise

Quality systems

GXP

Cross-functional leadership

Audits

Communication

Ausbildung

Bachelor’s degree

Advanced degree preferred

Jobbeschreibung

Description

JOB SUMMARY

The Vice President of Quality Assurance is responsible to implement and support strategies for Quality System processes and supporting technology, and ensuring the integrity, consistency, and harmonization of these processes and systems for Clinilabs.

This individual is also accountable for ensuring that the clinical activities are in compliance with current Good Clinical Practices (cGCP) and governmental regulations through creation and maintenance of quality and compliance systems within Clinilabs that monitor quality, efficiency, and uniformity of clinical trials and associated activities, both internally & externally.

This Vice President will provide regulatory expertise regarding all regulatory submissions for site services, clinical research organizations, client companies and internal project teams on regulatory requirements for all Clinilabs’ activities.

This Vice President will develop staff to meet expanding needs of the business and to prepare capable individuals for areas of higher responsibility. This individual must have ability to lead and mentor a team of staff to ensure all key activities and objectives are met.

RESPONSIBILITIES

• Provide leadership and direction to a growing quality and regulatory department
• Manage and provide leadership and organizational capability development for quality system, to ensure succession planning and performance standards remain at an optimal level
• Make decisions on process and system strategy recommendations, defining compliance-driven standards, determining boundaries for harmonization and alignment versus differentiation
• Provide leadership in setting strategy, implementing, and maintaining Clinilabs Quality Systems
• Act as quality systems subject matter expert and resource leader for focus areas by partnering with process owners to drive results by identification, selection, and/or facilitation skills
• Provide leadership and guidance for computer system and software validation, with particular focus on GCP / regulated systems
• Conduct internal and external audits in compliance with company SOPs
• Provide feedback to the quality control (QC) group
• Establish processes, standards, and procedures (as required); and ensure they remain current with regulatory requirements.
• Interact with FDA and other regulatory bodies
• Provide qualification audits of contractors and vendors, as needed
• Provide leadership and guidance on quality agreements
• Develop measures to monitor the effectiveness of the deployed quality system
• Identify potential quality issues and/or areas for improvement
• Monitor employee training and training program
• Oversight of controlled document management system
• Conduct / oversee Internal and external audits
• Develop and/or monitor vendor qualification program
• Other duties as assigned

Requirements

• The position requires at least a Bachelor’s degree, although advanced degrees are preferred.
• A minimum of 15 years working within GXP function is required.
• A minimum of 10 years of experience in a leadership role in quality and/or compliance is required.
• Proven experience in leading regulatory (FDA, MHRA, Etc.) inspection readiness, inspection activities, and responses
• Strong influencing, negotiations and leading without direct line authority experience is required.
• The ability to manage complexity and manage a diverse team is critical.
• Excellent written and oral communication and interpersonal relationship skills are required.
• Excellent leadership, influencing, and collaboration skills are expected.
• The selected candidate must come from a regulated industry.
• Ability to work and communicate in a cross-cultural environment is highly required.
• Previous experience driving performance results is required