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Job Summary: Professional responsible for developing and validating analytical methods for pharmaceuticals, ensuring quality and collaborating within multidisciplinary teams. Key Highlights: 1. Collaborate with multidisciplinary teams in product development 2. Study legislation and regulations for continuous updates 3. Analyze complex data and communicate results effectively We are a Brazilian pharmaceutical company dedicated to life for over 65 years. Guided by our purpose "transforming knowledge into health for your life", we have built our history with boldness, innovation, and visionary spirit. **Our reason for existence** is to promote high-quality health so people can enjoy every moment. We offer a broad portfolio of medications across multiple specialties—including gynecology, oncology, and cardiology—to comprehensively and individually serve patients with efficient and innovative formulations. We market over 100 brands across more than 200 presentations. **We want you to find your place here!** According to GPTW, we are recognized as an excellent workplace. We foster transparent and trusting relationships with our 3,000+ employees and encourage professional mobility as a key development tool. Health and well-being guide our decisions. **\#BecauseLifeIsTreated** **Responsibilities and Duties** **On a day-to-day basis, you will:** * Develop and propose stability-indicating analytical methods supporting drug development, through literature research, evaluation of reference/comparator drugs, and prior experience. * Challenge analytical methods and propose specifications for the finished product. * Develop and execute physicochemical assays according to project scope, preparing related documentation. * Collaborate with multidisciplinary teams in product development by proposing analytical solutions. * Jointly conduct product risk analysis targeting critical material attributes and critical process parameters that may impact critical quality attributes. * Continuously study current legislation and regulations to remain updated and contribute effectively to assigned projects. * Analyze complex datasets generated during development, interpret results to identify risks across the product lifecycle, and effectively communicate conclusions to stakeholders. * Perform analytical review, critically evaluating all generated documents and records, the rationale applied, calculations performed, and conclusions drawn. * Support responses to ANVISA requirements by providing technical information and conducting supplementary tests to formulate technical justifications. **Requirements and Qualifications** **To participate in our selection process:** * Bachelor’s degree in Chemistry or Pharmacy. * Experience with chromatographic techniques; * Experience in developing stability-indicating methods; * Experience with degradation profile studies per RDC 964\. * Experience with identification and qualification of organic impurities. * Knowledge of applied statistics for data analysis and stability trend evaluation. * Knowledge of risk analysis, AqbD, QbD, and DoE. * Knowledge of applied statistics for data analysis. * Intermediate to advanced English proficiency for reading, writing, and technical discussions with external partners. **You’ll stand out if you have:** * Postgraduate degree (Master’s and/or PhD) in Chemistry or Pharmacy, or related fields. * Knowledge of spectroscopic techniques; * Familiarity with chromatography software — OpenLab CDS. * Familiarity with statistical analysis software — Action Stat (Modules RDC 658, RDC 166, and RDC 318\). * Knowledge of risk analysis, statistical tools, and experimental design (AqbD, QbD, and DoE). * Knowledge of problem-solving tools. * Knowledge of degradation product modeling/simulation software. **Additional Information** **\+ Details** Work Location (Base): Embu das Artes Schedule: Monday to Friday – Flexible second shift (Start time between 11:00–14:00; end time between 20:00–22:30\). **For Libbs Employees** * Applications accepted until **03/26/2026\.** * Preferred qualifications may be prioritized during candidate selection for the next stage; * Simultaneous participation in different internal selection processes is not permitted. **Benefits for You!** * Meal Voucher; * Food Voucher; * Libbs Medications — 100%; * Pharmacy Benefit — Vidalink; * PPR — Profit and Results Sharing Program; * Parking, transportation voucher, or shuttle service (applicable only for shift-based roles); * USE Program: subsidy for purchasing work equipment, usable for personal purposes; * Flexible benefits (TotalPass, life insurance, private pension, medical and dental assistance, food allowance). We are a Brazilian pharmaceutical company dedicated to life for over 67 years. Guided by our purpose "transforming knowledge into health", we have built our history with boldness, innovation, and visionary spirit. Here, we believe **diversity** strengthens our purpose and relationships. All positions are evaluated with inclusion in mind, focusing on competency-based assessment. **Our reason for existence** is to promote high-quality health so people can enjoy every moment. We offer a broad portfolio of medications across multiple specialties—including gynecology, oncology, and cardiology—to comprehensively and individually serve patients with efficient and innovative formulations. We market over 100 brands across more than 240 presentations. **We want you to find your place here!** According to GPTW, we are recognized as an excellent workplace. We foster transparent and trusting relationships with our 3,900+ employees and encourage professional mobility as a key development tool. Health and well-being guide our decisions. We operate a manufacturing unit in Embu das Artes, logistics centers in Embu and Varginha, and our administrative team works fully remotely, with access to coworking spaces worldwide.
