Senior Documentation Good Practices Analyst

Description

Job Summary: Professional to work as a Senior Documentation Good Practices Analyst, performing medium-complexity tasks in technical documentation and quality. Key Highlights: 1. Experience in the pharmaceutical industry 2. Focus on technical documentation and data integrity (GDP) 3. Opportunity for professionals in Pharmacy, Chemistry, and Biology **The Seres Group, in partnership with a national company in the pharmaceutical industry segment, is seeking a professional for the role of Senior Documentation Good Practices Analyst.** **Responsibilities:** * Perform, with technical proficiency and initiative, medium-complexity tasks within the Documentation Good Practices Service related to technical documentation, issuing technical opinions and disseminating results in reports; reviewing and critically analyzing operational procedures and analytical documentation; evaluating and dispositioning control plans in the system; reconciling and dispositioning finished product batches in the system; approving graphic artworks; monitoring and releasing technical specifications; creating and approving formulations and resources in the system; participating in investigation laboratories; evaluating and approving graphic artworks; supporting audits; monitoring CAPA actions; preparing impact assessments for change management; contributing to the company's training program; serving as an instructor for training sessions related to procedures and topics on Good Manufacturing Practices and quality; promoting the use of process analysis and improvement methodologies; developing performance indicators based on process modeling decomposition, aiming to enhance quality; ensuring compliance with SOPs and the institution’s Good Manufacturing Practices. **Working Hours:** * Schedule: 8:00 AM to 5:00 PM * Shift: Monday to Friday * Work Model: On-site **Work Location:** * Jacarepaguá, Rio de Janeiro \- Brazil. We encourage applications from persons with disabilities (PCD), Black individuals, women, and LGBTQIAPN\+ individuals. **Mandatory Requirements:** * Bachelor’s degree completed in Pharmacy, Chemistry, Biology, or related fields; * Experience in technical documentation and data integrity – GDP in the pharmaceutical industry; * Intermediate English proficiency; * Proficiency in Microsoft Office suite, especially Excel; **Desirable Qualifications:** * Preferred qualification and/or residency in Pharmaceutical Industry, Pharmaceutical Technology, or other areas related to pharmaceutical management, manufacturing, and drug quality; * SAP system experience is a plus. Minimum Educational Requirement: Bachelor’s Degree