Analytical Support Specialist

Description

Position Summary: We are seeking an Analytical Support Specialist to ensure continuity, reliability, and traceability of analytical processes, regulatory compliance, and quality management in the pharmaceutical industry. Key Highlights: 1. Participates in the preparation and execution of stability studies. 2. Ensures analytical planning and management of laboratory supplies. 3. Ensures compliance with quality and safety regulations. **Analytical Support Specialist** Have you ever felt exhausted by bureaucracy? So have we. That’s why we’re changing the way we work—to boost productivity, accelerate innovation, and deliver better results. We call it **Dynamic Shared Ownership (DSO)**. Learn more about what DSO means for you in your new role here https://www.bayer.com/en/strategy/strategy **KEY RESPONSIBILITIES** * Participates in document preparation, test execution, result analysis, and generation of evidence demonstrating that stability studies and analytical methods are suitable, accurate, reproducible, and fit for purpose—ensuring continuity, reliability, and traceability of analytical processes. * Ensures analytical planning by guaranteeing availability of supplies required for analytical activities in laboratories; also prevents procurement of non-consumed materials to avoid economic waste and minimize potential environmental impacts, following supplier selection and approval. * Manages and/or places purchase requests for analytical laboratory supplies to ensure timely availability, and enters supplies into the system while managing applicable inventory. * Performs laboratory equipment maintenance, calibration, and/or qualification activities to ensure operation within specifications—thereby ensuring reliability of analytical results and continuity of operations. * Ensures implementation and dissemination of core Quality Management System (QMS) regulations (policies, SOPs, operating instructions, etc.) applicable to physicochemical determinations, as well as implementation of new regulations (if required). * Ensures compliance with quality subsystems (deviations, changes, CAPAs, complaints, OoS/OoT, continuous training) per current procedures—documenting promptly and following established workflows. * Leads the development of effective quality control processes, including trend monitoring and analysis, evaluation of relevant business KPIs, and supports quality control improvement projects. * Ensures compliance with quality, safety, environmental impact, and hygiene standards. Additionally ensures participation in and development of other quality control–related activities or projects as needed. **WHO YOU ARE** * Education: Bachelor’s degree * Profession: Related to the pharmaceutical field (medicines/APIs) * Work experience: Minimum 1 year in the pharmaceutical industry * Knowledge of regulations related to Good Manufacturing Practices (GMP), national and international Good Laboratory Practices (GLP), analytical safety regulations, physicochemical and microbiological analytical testing, pharmacopoeia handling, analytical methodologies, reagent preparation, among others. * Languages: Basic to intermediate English * Competencies: Customer orientation, observant, analytical thinking, complexity management, results-driven, teamwork, planning, self-learning, decision-making, high level of commitment. At Bayer, we believe in diversity, equity, and inclusion. Our goal is to create a workplace where everyone can feel authentic, respected, and equally valued. Every day, we strive to reflect our values through the unique capabilities, experiences, and aspirations of our people. We intentionally seek diversity—and thereby empower our people to reach their full potential and encourage others to do the same. Candidates who meet the requirements outlined in the job profile will be considered for employment regardless of disability, race, color, religion, sex, age, sexual orientation, gender identity, and will not be disadvantaged if unemployed. **Application Period:** 12/05/2026 \- 25/05/2026 **Reference Code:** 868480 **Division:** Pharmaceuticals **Location:** Costa Rica : Heredia : Heredia \|\| Mexico : Veracruz : Orizaba **Functional Area:** Quality **Work Time:** Full-Time **Employment Type:** Regular **Location** Orizaba