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Job Summary: The professional will operate machines with different technologies, perform setups and adjustments, monitor production, and inspect products, ensuring quality and compliance with Good Manufacturing Practices. Key Highlights: 1. Opportunity to operate diverse and specialized machinery. 2. Focus on production quality and Good Manufacturing Practices (GMP). 3. Encouragement of mobility and professional development. We are a Brazilian pharmaceutical company dedicated to life for over 65 years. With the purpose of "transforming knowledge into health for your life", we have built our history with boldness, innovation, and visionary spirit. **Our reason for being** is to promote high-quality health so people can enjoy every moment. We offer a broad portfolio of medications across various specialties—such as gynecology, oncology, and cardiology—to comprehensively and individually serve patients, with efficient and innovative formulations. We have 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 place to work. We foster transparent and trusting relationships with our 3,000+ employees and encourage mobility as a tool for professional development. Health and well-being guide our decisions. **\#BecauseLifeIsTreated** **Responsibilities and Duties** **On a daily basis, you will:** * Operate all machines with different technologies, master setup and adjustment procedures, and be capable of sharing knowledge; supply required materials, monitor production, ensure proper equipment operation, detect issues, and collaborate with maintenance when necessary to support interventions and root cause analysis, thereby ensuring product manufacturing quality and line performance expectations; * Be responsible for cleaning and operating the production line—including machines, equipment, and utensils—during SETUP and operation phases; perform hygiene procedures on equipment, production machines, utensils, and the environment using specific cleaning agents; verify their integrity and working conditions; mark verified items on the checklist form and complete the document for line release, ensuring adherence to the production plan and compliance with GMP standards; * Be responsible for inspecting products on production lines at the start, during, and upon completion of the production process; conduct physical tests and record information to ensure product quality and forward samples to the Quality Control department for required analyses; * Be responsible for the production process, ensuring original conditions and physical attributes, product quality, and verifying damages or modifications to guarantee that the production process phase meets required specifications; * Support validation testing and development of new product manufacturing processes through pilot batch production; monitor preventive maintenance on area equipment; and execute tests of new materials and tooling by documenting performed tests, ensuring test history and reliability; * Provide support to immediate supervisors regarding production scheduling control, document closure, and investigation of production deviations, when necessary; * Ensure counting and reconciliation of material rejects generated during production, properly handle production rejects by completing all relevant documentation, transporting them to the production waste department, and informing cleaning staff to take appropriate action—thus preventing mixing of approved products with rejects; * Perform distinct production processes and possess the ability to detect issues and collaborate with maintenance when necessary to support interventions and root cause analysis; fully handle productive inputs according to manufacturing techniques to obtain bulk material for the next stage. **Requirements and Qualifications** **To participate in our process:** * Completed high school education; * Experience handling solid dosage forms; * Experience with compression and coating machine operations and related processes; * Knowledge of Good Manufacturing Practices (GMP); * Preferred experience in a pharmaceutical environment, preferably with oncology products; * Experience with process documentation and recordkeeping; * Experience in bulk product packaging. **Additional Information** **\+ Information** Work Location: Embu das Artes \- São Paulo Schedule: **6x1 rotating shift – 1st shift (6:00 AM–2:20 PM) and 2nd shift (2:00 PM–10:17 PM)** **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 for shift work and subject to availability of routes serving regions within a straight-line radius of up to 40 km from the facility); * Flexible benefits (life insurance, private pension, medical and dental assistance, food allowance). We are a Brazilian pharmaceutical company dedicated to life for over 67 years. With the purpose of "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 an inclusion focus, respecting competency-based assessment. **Our reason for being** is to promote high-quality health so people can enjoy every moment. We offer a broad portfolio of medications across various specialties—such as gynecology, oncology, and cardiology—to comprehensively and individually serve patients, with efficient and innovative formulations. We have 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 place to work. We foster transparent and trusting relationships with our 3,900+ employees and encourage mobility as a tool for professional development. 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 100% remotely, with access to coworking spaces worldwide.
