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Director of Quality, Pharmaceuticals
📍 Relocation to a region in the Russian Federation
Responsibilities: • Leadership of the Quality Department (Quality Control Department, Quality Assurance Department, Validation, Pharmacovigilance) – task setting and coordination. • Preparation for external audits (regulators, contractors) and control of internal self-inspections, supplier audits. • Ensuring and developing the Quality Management System in accordance with GMP. • Organization of documentation flow, development and implementation of SOPs and standards. • Quality control at all stages, process validation, method validation, and qualification of equipment/engineering systems. • Leadership of investigations of deviations, non-conformities, complaints. Management of risks to the quality of medicinal products. • Training and mentoring of employees.
Requirements: • Higher specialized education (chemistry, biology, pharmacy, medicine, etc.). • At least 3 years of management experience in a quality department at a pharmaceutical enterprise is mandatory. • Successful GMP inspections and licensing. • Knowledge of the Russian Federation legislation regarding medicinal products circulation and GMP standards. • Skills in negotiation, project management, presentations.
Conditions: • Large developing enterprise. • Full relocation package. • Official employment according to the Labor Code of the Russian Federation, official salary. • 5/2 work schedule. • Social package: Voluntary Medical Insurance (including dental care), meal compensation, corporate transportation, events, gifts for employees and children. • Career and professional growth.
Everything about career development
Russia
Relocation
from 3 years
Experience
Full-time
Employment
Onsite
Work Format
Director
Grade
Management
Specialization
MedTech
Industry
Corporation
Company Type
By country
Director
Grade
Management
Specialization
MedTech
Industry
Corporation
Company Type