QA Site Officer / Validation & Qualification

Description

Job Summary: Ensures the application of pharmaceutical quality standards by managing changes, deviations, and process validations within a cGxP environment. Key Highlights: 1. Ensure the correct application of pharmaceutical quality standards. 2. Manage change controls, deviations, and CAPA. 3. Opportunities for development and continuous learning. **Mission** Under the supervision of the QA Senior Site Manager / QP, ensures the correct application of Ferrer’s internal standards and reference standards of the Pharmaceutical Quality System as defined in EU cGxP and 21 CFR Parts 210 & 211 cGxP within assigned areas of responsibility and where applicable. Implements the Quality Assurance program at the respective site according to the Corporate Pharmaceutical Quality System reference standards, ensuring both its correct implementation and continuous improvement. **Responsibilities** * Ensure management within the scope of responsibility in accordance with the principles of the Corporate Quality System. * Manage change controls, deviations, and CAPA. * Review batch records and manage information in related computerized systems. * Provide objective data periodically and participate in preparing quality-related reports and indicators within the scope of responsibility. * Execute qualification programs for equipment, facilities, utilities, and computerized systems. * Execute validation programs for manufacturing processes and cleaning procedures. * Prepare PQR/APR reports for products manufactured at the Plant. * Provide support and participate, as required, in internal and external audits and regulatory inspections. **Why Ferrer?** * Positively impact society. * Opportunity to participate in volunteer initiatives. * Corporate culture based on trust and responsibility. * Opportunities for development and continuous learning. * Meal vouchers in case of split shifts. * Flexible compensation. * People Support Plan (psychological, legal, and financial counseling). If you are empathetic, humble, curious, and optimistic, Ferrer is your company! You will excel in this role if you meet the following criteria: * Degree in Pharmacy or equivalent. * A Master’s degree in Pharmaceutical and Parapharmaceutical Industry is desirable. * Minimum 3 years’ experience in a similar position managing validations and/or qualifications in the pharmaceutical industry. * English B2. * Skills and Competencies: + Person aligned with company values: empathetic, humble, curious, and optimistic. + Organized individual with ability to cooperate across diverse environments. + Proactive both individually and within team settings. If you believe your profile fits and you are eager to embark on an exciting new project, we are waiting for you! At Ferrer, we guarantee equal treatment and opportunities in hiring, avoiding prejudice and stereotypes for any reason during access-to-employment processes, evaluating only objective criteria such as professional competencies, academic qualifications, and work experience.