Quality Assurance Manager

Descompagnons Trabalho Temporário Lda; Viseu; Presencial; EUR 30 000 - 40 000; Tempo integral

Resumo da oferta

A leading pharmaceutical company is seeking a Quality Assurance Manager in Viseu, Portugal. The ideal candidate will manage the QA team, develop quality assurance plans, and ensure compliance with GMP standards. A Bachelor or Master’s degree in Pharmaceutical Sciences and a minimum of 3 years in a regulated organization are required. This role offers a competitive salary along with other benefits.

Serviços

Base salary + benefits

Initial and continuous training

Dynamic team environment

Qualificações

• Minimum of 3 years of experience in a regulated organization.
• Experience in ISO, GLP, GMP, QMS or similar.
• Fluent in written and spoken English.

Responsabilidades

• Manage the Quality Assurance Team.
• Develop, review, approve and maintain SOPs.
• Oversee compliance audits and quality inspections.

Conhecimentos

Leadership

Communication skills

Knowledge of GMP

Problem-solving

Formação académica

Bachelor or Master’s Degree in Pharmaceutical Sciences

Ferramentas

MS Office

Descrição da oferta de emprego

Overview

Pharmaplanet is a pharmaceutical laboratory, but also a company that provides specialized services in scientific and commercial areas. We offer solutions such as brand promotion and consultancy services for modern companies across various segments of the healthcare sector.

We are looking for a Quality Assurance Manager for a project working directly with our client, a leader in the manufacturing and packaging of pharmaceutical products.

Responsibilities

• Manage the Quality Assurance Team
• Manage and oversee company quality assurance policies
• Maintain a Pharmaceutical Quality System according to GMP (Good Manufacturing Practices)
• Develop, review, approve and maintain SOPs (Standard Operating Procedures) and quality assurance procedures
• Assist with training staff on various practices and on standard operating procedures (SOPs) for new or updated processes
• Work closely with other teams to implement changes to increase efficiency and to identify and establish corrective actions while still maintaining high levels of quality
• Supervise the life cycle of the products in place to ensure each step is completed correctly and confirm that cannabis products are up to standards
• Assist Qualified Person (QP) with recalls and complaints investigation and ensure they are performed according to quality and regulatory requirements
• Develop quality assurance plans by conducting hazard analyses, identifying critical control points and preventative measures, establishing critical limits, monitoring procedures, corrective actions, and verification procedures
• Manage site quality inspection activities, schedule and participate in compliance audits and, where applicable, supplier quality assessments
• Manage and support the validation and qualification studies
• Manage the Change Controls and Deviations raised within the Quality System
• Perform any other duties that may arise from time to time as a team, and as requested by the QP

Requirements

• Bachelor or Master’s Degree in Pharmaceutical Sciences, Chemistry or related
• Minimum of 3 years of experience in a regulated organization for the production of medicines
• Experience/knowledge demonstrated in ISO, GLP, GMP, QMS or similar
• Knowledge of written and spoken English
• Ability to work in a result‑oriented, challenging environment
• Ability to react to urgent situations and leadership capacity
• Excellent interpersonal and communication skills, including speaking and writing
• Computer knowledge from the MS Office user perspective

Offer

• Employment contract directly with the client
• Base salary + other benefits offered by the client
• Initial and continuous training
• Integration into a dynamic and ambitious team

Ref: QASM_SHII25

Submit your application through our website or by email.

Note: Due to the expected high volume of applications, it will not be operationally possible to provide feedback to all candidates. Only shortlisted candidates will be contacted within 15 days.

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