Quality Assurance Manager

Client 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. Job description Manage the Quality Assurance Team; Manager to 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 lifecycle of the products in place to ensure each step is completed correctly done 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; Develops quality assurance plans by conducting hazard analyses, identifying critical control points and preventative measures, establishes 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. procedures. Offer Employment contract directly with the cliente; Base salary + other benefits offered by the client; Initial and continuous training; Integration into a dynamic and ambitious team. Work location: Catanhede 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. By submitting your CV, you consent to the processing of your personal data for recruitment purposes, in accordance with our Privacy Policy available on our website. Your data will be stored securely and will not be shared with third parties without your consent. You may access, correct, delete, restrict, or object to the processing of your data. The data will be retained for this and future recruitment processes. For more information or to exercise your rights, please refer to the Privacy Policy. Tipo de oferta: Integral/Full-time