Site Quality Head: GMP/ISO Leader, Global QA Strategy

Siegfried AG; Barberà del Vallès; On-site; EUR 90,000 - 150,000; Full time

Benefits offered by this job

Annual Bonus

Company car

Free parking

Canteen on-site / restaurant tickets

Medical, life, and accident insurance

Club Siegfried access

Job summary

Siegfried AG is seeking a Site Quality Head to manage QA and QC, aligning operations with the overall quality strategy. Lead budgets, resources and policies to ensure compliance and continuous improvement across site activities.

The role requires pharmacy qualifications, regulatory knowledge, and proven leadership in a pharmaceutical CDMO environment. English and local language skills are essential; audits and multi-client management experience are highly valued.

Qualifications

• Experience in pharmaceutical CDMO environment is strongly preferred.
• Exposure to customer audits, regulatory inspections, technology transfers and multi-client management is required.
• Experience in managing large teams.

Responsibilities

• Ensure GMP, ISO 13485, ICH compliance across site operations.
• Lead QA and QC functions and related budget planning.
• Ensure site products and decisions meet Siegfried Quality requirements.
• Act as primary point of contact for Global Quality matters and policy adherence.
• Drive continuous improvement and quality-first culture site-wide.
• Provide leadership for product quality, patient safety and regulatory compliance.
• Oversee Site Quality Strategy and align with corporate objectives.
• Act as Medical Devices Management Representative per ISO 13485.
• Ensure SHE requirements and standards are met.

Skills

Regulatory knowledge (FDA MHRA EMA WHO

English proficiency

Leadership

Quality systems

Education

Pharmacy degree

MBA valued

Job description

Siegfried AG is seeking a Site Quality Head to manage QA and QC, aligning operations with the overall quality strategy. Lead budgets, resources and policies to ensure compliance and continuous improvement across site activities.

The role requires pharmacy qualifications, regulatory knowledge, and proven leadership in a pharmaceutical CDMO environment. English and local language skills are essential; audits and multi-client management experience are highly valued.