Novo Oriente Trades Services Job Listings

Bio Ritmo | Junior Sales Consultant | Santander65178116413825120

Indeed

Bio Ritmo | Junior Sales Consultant | Santander

Job Summary: We are looking for someone to handle reception and customer service, access control, and problem resolution in a collaborative and constantly evolving environment. Key Highlights: 1. Relaxed and collaborative work environment 2. Focus on customer service and problem resolution 3. Opportunity at a leading company in the fitness sector Brazil **What is the work environment like?** We strive to maintain a relaxed environment where everyone’s opinion influences team decisions. We work collaboratively and creatively. We are constantly evolving and always open to new trends. **Responsibilities of the Role** * Reception and Customer Service: Greet customers and visitors, provide information about gym services, and address inquiries. * Access Control: Monitor member and visitor access, ensuring courteous and efficient service. * Problem Resolution: Handle customer issues efficiently and professionally. * Support sales service as needed **Requirements** Completed high school education. Preference given to candidates currently pursuing higher education (physical education or related fields). **Benefits** * Gym / Sports Activities * Medical Assistance * Dental Assistance * Product Discounts * Life Insurance * Corporate University * Commuter Allowance **About the Organization** The Smart Fit Group owns full-service gym brands Smart Fit & Bio Ritmo, studio gym brands Race Bootcamp, Vidya Body & Mind, Tonus Muscle Lab, Jab House and Nós, as well as digital products Total Pass and Queima Diária. Together, our brands operate over 800 locations and serve more than 2.5 million active customers. We are present in Brazil, Mexico, Chile, Peru, Colombia, Dominican Republic, Ecuador, Argentina, Panama, Guatemala, Paraguay, El Salvador and Honduras. We are the largest fitness company in Latin America and the third largest worldwide.

Brazil

Pharmaceutical Process Consultant64843290036867121

Indeed

Pharmaceutical Process Consultant

**Your mission will be:** ---------------------- This position is part of the MSAT (Manufacturing Sciences and Technology) team, which is responsible for ensuring process robustness throughout the entire product lifecycle for paste technologies. You will be responsible for evaluating process data, identifying opportunities, and implementing improvements to pharmaceutical manufacturing processes, with the objectives of: reducing process losses, decreasing the number of deviations, increasing process robustness and reliability, and reducing industrial, regulatory, and recall risks. **Roles and Responsibilities:** ------------------------------- * Lead implementation of improvement projects at the Paulínia manufacturing site for Semi-Solid/Paste technologies; * Lead Scale-Down/Quality-by-Design projects for semi-solid/paste products; * Deliver project progress reports and presentations; * Collaborate with Global/Local teams to execute parallel projects, ensuring the sustainability of semi-solid/paste products at the PLN site; * Define QTTP, CQA, and CMA for newly developed products; * Collect and analyze process data (using statistical tools) starting from the definition phase; * Implement MSAT-defined projects related to semi-solid/paste products; * Provide technical assessments and process validation strategies for material and supplier change projects; * Analyze historical data when resolving issues and proactively support the application of Design of Experiments (DoE) to identify risks and enhance current process robustness or productivity; * Reduce industrial risks, conduct process risk analyses, and proactively propose improvements to process robustness, reliability, and safety; * Respond to regulatory audits such as MAPA, FDA, and ANSES. **And what do you need to fulfill your mission? (Requirements)** ------------------------------------------------------------------ **Required:** --------------- * Bachelor’s degree in Pharmacy, Chemical Engineering, Food Engineering, Production Engineering, Materials Engineering, or related fields; * Experience in Semi-Solid Development; * Strong knowledge of industrial processes; * Extensive experience in manufacturing/filling of semi-solid/paste products; * Advanced English proficiency. **Desirable:** * Experience working in companies regulated by FDA, ANSES, and MAPA; * Green Belt or Black Belt certification (preferred); * Postgraduate degree in Industrial Process Management, Engineering, Pharmacy, or Project Management.

GWX2+X2 Alívio, São Miguel do Tapuio - PI, Brazil

Quality Control Technician - Affirmative position for professionals with disabilities64365234319745122

Indeed

Quality Control Technician - Affirmative position for professionals with disabilities

**Your mission will be:** ---------------------- This is an affirmative recruitment position for **professionals with disabilities.** At Boehringer Ingelheim, we are driven by our people. That is why we are committed to cultivating a diverse, collaborative, open, and inclusive environment where everyone feels safe, heard, and valued. This workplace culture that embraces differences is key to innovation, value creation, and sustainable growth both within and beyond our organization. The selection process for this position follows the same steps and evaluation methods as other Boehringer Ingelheim recruitment roles. Ensure the execution and guidance of sampling activities, laboratory analyses, quality inspections, and input management, guaranteeing compliance with technical and regulatory standards. Responsible for maintaining laboratory organization, calibrating equipment, preparing solutions, operating systems, training staff, and supporting monitoring programs (water, cleaning, and 5S), aiming for quality, safety, and efficiency in processes. **Roles and Responsibilities:** ------------------------------- * Perform sampling of Packaging Materials, Graphic Arts, Raw Materials, Stability, Intermediate Product, Finished Product, Water, and Cleaning according to release priorities established in TIER meetings, spreadsheets, SAP system, and alignment with Supervision; * Carry out receiving of Materials, technical stock, Stability, Finished Product, Water, and Cleaning; * Conduct analyses on packaging materials, graphic art, raw materials, finished and intermediate products, inspection of intermediate and finished products, quality inspections on production lines, reading and recording of activities, management of retention and reference samples; * Perform periodic cleaning of sampling rooms according to established procedures; * Operate software related to Sampling, Receiving, Technical Stock, Stability, and Glassware Cleaning activities; * Complete forms, reports, logbooks, and general documents related to Materials, Stability, Finished Product, Water, Cleaning, and glassware cleaning activities in the laboratory; * Verify the integrity of Materials received on site, identify and report damages; * Verify the integrity of inputs received on site, identify, report damages, and proceed with invoice forwarding; * Report any discrepancies, missing materials, or risks during processes; * Report team plan fulfillment at the end of the work shift in TIERS or to supervision; * Provide guidance and training to the team whenever necessary; * Carry out and/or contribute to procedure reviews when needed; * Seek, identify, and implement process improvements; * Complete training and follow procedures for each process to be executed; * Conduct training within established deadlines; * Verify labels, forms, and general documentation; * Ensure maintenance of stocks of all sampling and laboratory analysis supplies; * Check and organize stocks of all sampling and laboratory analysis supplies; * Support the shipment of outsourced samples; * Ensure compliance with Quality requirements; * Ensure compliance with HSE requirements; * Ensure compliance with data integrity requirements; * Support other colleagues in their activities when necessary due to emergencies, vacations, or absences; * Operate pallet jacks in warehouses according to current procedures; * Report analytical data accurately due to high volume of records; * Ensure proper cleaning of glassware as required; * Assist in maintaining equipment in use and under qualification in the laboratory; * Contribute to maintaining the stability program; * Prepare Mobile Phase Solutions, Reagents, Volumetrics in the Analytical Laboratory; * Perform Verification/Calibration of Analytical Laboratory equipment; * Accurately complete documentation, labels, bench sheets, logbooks, or analytical documentation in general in the Quality Control laboratory; * Perform correct disposal of Reagents, solutions, and Materials in the Laboratory as indicated in laboratory procedures; * Conduct inventory checks of analytical supplies and prepared reagents to keep the laboratory stocked; * Organize materials and reagents, remove expired items, label cabinets, contribute to overall laboratory organization; * Follow analysis scheduling according to standard work. **And what do you need to accomplish your mission?** --------------------------------------------------- **Required:** --------------- * Technician in Chemistry, Biochemistry, Pharmacy, or related fields; * Experience in raw material sampling; * Analysis of raw materials; * Experience in the pharmaceutical industry; * Good Laboratory Practices; * Basic knowledge of Office suite; * Good writing skills; * Communication skills; * Initiative; * Organization; * Teamwork; * Good interpersonal relationships; Basic English. * **Desirable:** --------------- * Experience with RAMAN sampling equipment; * Experience in bench analysis (Karl Fisher), pharmacopoeial tests (pH, Density, Melting Point, Titration, Loss on Drying); * Experience in chromatographic analysis (HPLC and GC).

GWX2+X2 Alívio, São Miguel do Tapuio - PI, Brazil

Quality Control Technician - Fixed Term64365234335617123

Indeed

Quality Control Technician - Fixed Term

**Your mission will be:** ---------------------- Ensure the execution and guidance of sampling, laboratory analyses, quality inspections, and input management activities, guaranteeing compliance with technical and regulatory standards. Responsible for maintaining laboratory organization, calibrating equipment, preparing solutions, operating systems, training staff, and supporting monitoring programs (water, cleaning, and 5S), aiming at quality, safety, and process efficiency. **Roles and Responsibilities:** ------------------------------- * Perform sampling of Packaging Materials, Graphic Arts, Raw Materials, Stability, Intermediate Product, Finished Product, Water, and Cleaning according to release priorities established in TIER meetings, spreadsheets, SAP system, and alignment with Supervision; * Perform receipt of Materials, technical inventory, Stability, Finished Product, Water, and Cleaning; * Conduct analyses on packaging materials, graphic art, raw materials, finished and intermediate products, inspection of intermediate and finished products, quality inspections on production lines, reading and recording of activities, management of retention and reference samples; * Perform periodic cleaning of sampling rooms as per established procedures; * Operate software related to Sampling, Receipt, Technical Inventory, Stability, and Glassware Cleaning activities; * Complete forms, reports, logbooks, and general documents related to Materials, Stability, Finished Product, Water, Cleaning, and glassware cleaning activities in the laboratory; * Verify the integrity of Materials received on site, identify and report damages; * Verify the integrity of inputs received on site, identify, report damages, and proceed with invoice routing; * Report any discrepancies, material shortages, or risks during processes; * Report team plan compliance at the end of the work shift in TIERS or to supervision; * Provide guidance and training to the team whenever necessary; * Perform and/or contribute to procedure revisions when needed; * Seek, identify, and implement process improvements; * Complete training and follow procedures for each process to be executed; * Conduct trainings within established deadlines; * Verify labels, forms, and general documentation; * Ensure maintenance of all sampling and laboratory analysis input inventories; * Check and organize all sampling and laboratory analysis input inventories; * Support the shipment of outsourced samples; * Ensure compliance with Quality requirements; * Ensure compliance with HSE requirements; * Ensure compliance with data integrity requirements; * Support other colleagues in their activities when necessary due to urgencies, vacations, or absences; * Operate pallet jacks in warehouses according to current procedures; * Report analytical data accurately due to high volume of records; * Ensure glassware cleaning as required; * Assist in maintaining equipment in use and under qualification in the laboratory; * Support the stability program maintenance; * Prepare Mobile Phase Solutions, Reagents, and Volumetric solutions in the Analytical Laboratory; * Perform Verification/Calibration of Analytical Laboratory equipment; * Accurately complete documentation, labels, bench sheets, logbooks, or analytical documentation in general in the Quality Control laboratory; * Perform proper disposal of Reagents, solutions, and Materials in the Laboratory as indicated in laboratory procedures; * Conduct assessments of analytical inputs and prepared reagents to keep the laboratory supplied; * Organize materials and reagents, remove expired items, perform cabinet labeling, contribute to overall laboratory organization; Follow analysis scheduling according to standard work. * **And what do you need to accomplish your mission?** --------------------------------------------------- **Required:** --------------- * Technician in Chemistry, Biochemistry, Pharmacy, or related fields; * Experience in raw material sampling; * Analysis of raw materials; * Experience in pharmaceutical industry; * Good Laboratory Practices; * Basic knowledge of Office suite; * Good writing skills; * Communication skills; * Initiative; * Organization; * Teamwork; * Good interpersonal relationships; * Basic English. **Desirable:** --------------- * Experience with RAMAN sampling equipment; * Experience in bench analysis (Karl Fisher), pharmacopoeial tests (pH, Density, Melting Point, Titration, Loss on Drying); * Experience in chromatographic analyses (HPLC and GC).

GWX2+X2 Alívio, São Miguel do Tapuio - PI, Brazil

Senior Quality Control Operator (Temporary for 1 year)64365234351235124

Indeed

Senior Quality Control Operator (Temporary for 1 year)

**Your mission will be:** ---------------------- Be a technical reference in the aseptic process area, working on process flow improvements and supporting the operational team. Perform and support microbiological quality control activities, including material preparation, analyses, and environmental monitoring. Conduct microbiological tests, record data in systems, and maintain laboratory organization. Contribute to document reviews, corrective actions, and training. Interact with related areas, ensuring compliance and efficiency. **Roles and Responsibilities:** ------------------------------- * Follow described work procedures/instructions to achieve quality and safety results within the Quality Control department in Paulínia. * Participate in More Green and Be Safe Transformation program initiatives, report EHS events (accidents, near\-misses, and environmental impacts), collaborate in inspections and investigations when requested, and attend mandatory EHS trainings. * Ensure compliance with data integrity requirements – Data Integrity / ALCOA\+. * Ensure traceability and integrity of data through records of sample in/out (products, raw materials, process controls), inputs/reagents/analytical materials, using an appropriate sample management tool/system and status tracking. * Collaborate in maintaining inventories of all inputs, reagents, and analytical materials. * Assist in maintaining laboratory equipment (in use/qualification), operating instruments and equipment used in analyses under your responsibility according to current procedures. * Support the preparation of materials, solutions, and culture media for analyses, as well as routines for cleaning/washing materials, sterilization, and waste disposal. * Perform sampling for environmental, personnel, process (e.g.: bioburden), and cleaning monitoring, adhering to schedules, frequency, and collection plans. * Perform sampling for environmental, personnel, process (e.g.: bioburden), and cleaning monitoring in aseptic processing areas (clean room), according to schedule. * Perform water, bioburden, and incubation analyses according to procedures, reporting analytical data in compliance with ALCOA\+, meeting analysis planning and defined work instructions. * Perform incubation and reading of environmental monitoring, as well as reading of performed analyses. * Contribute to the creation and review of documents (procedures, forms, etc.), investigation of analytical failures, incidents, discrepancies, and provide training and coaching for Junior Operators, ensuring adherence to current procedures, as well as contributing to operational improvements. * Collaborate with the implementation of preventive and corrective actions arising from discrepancies, events, OOX, internal or external audits. * Contribute to and participate in Housekeeping activities. * Support internal site customers. **What do you need to accomplish your mission?** --------------------------------------------------- **Required:** --------------- * High school diploma. * Proficiency in microbiological laboratory techniques. * Aseptic technique and ability to read pharmacopoeial compendia. * Knowledge of GMP (Good Manufacturing Practices) and aseptic practices. **Desired:** --------------- * Technical degree in Chemistry, Biochemistry, or Pharmacy. * Courses in Good Laboratory Practices (GLP) or specialization in Microbiology, Quality Control, or related fields. * Experience in regulated environments such as pharmaceutical or cosmetic industries. * Knowledge of compendia (USP, EP, etc.). * Internal training in sampling and validation. * Experience in technical investigations.

GWX2+X2 Alívio, São Miguel do Tapuio - PI, Brazil

Indeed

Electrician

Company hires Electrician in Crateús. **Responsibilities:** Install electrical systems, such as wiring, circuit breakers, outlets, and switches. Perform preventive and corrective maintenance on electrical systems, identifying and fixing issues. Conduct tests and measurements on electrical systems to ensure proper operation. Interpret electrical designs and follow technical and safety standards. Identify and correct faults in electrical systems, such as short\-circuits and overloads. Perform grounding and protection against electrical surges. **Compensation:*** Salary: To be negotiated. * Benefits: To be negotiated. **Additional Information:*** Contract: Permanent * Period: Full time * Schedule: To be negotiated. ***Work Location:*** *On\-site in Crateús / CE* ***Application Deadline:*** *11/11/2025* ***Expected Start Date*** *19/11/2025* ***JobId.:*** *29380296505* *✔ Follow:* ***@jobbol.empregos*** *on Instagram and get the best of the 2025 job market\.*

R. Bento Vieira Lima, 72 - Fatima I, Crateús - CE, 63703-075, Brazil