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Laboratory & Technical Services in San Martin Hidalgo
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Location:San Martin Hidalgo
Category:Laboratory & Technical Services
Water Treatment Analyst64241508333313120
Indeed
Water Treatment Analyst
**JOIN OUR TEAM AS A WATER TREATMENT ANALYST!** This is your opportunity! A leading agribusiness company specializing in sugar production is looking for your skills and expertise. **What is your main responsibility?** * Hourly sampling of pure, vegetable, and ammoniacal condensates. * Analysis of hourly parameters of condensates. * Interpretation of boiler water analysis for the application of chemical water treatment. **What we are looking for in you:** * **Education:** Chemical Technician or related field. * **Knowledge:** Excel, Office suite, Basic chemical analysis. **What we offer?** * **Competitive salary** based on your experience. * **Benefits exceeding legal requirements** and opportunities for growth. **Are you interested in developing your career at one of Mexico's top companies?** Apply now through this platform and we will contact you.
Frambollan 32, Gamboa, 45308 Tala, Jal., Mexico
Negotiable Salary
LABORATORY MANAGER64155948834945121
Indeed
LABORATORY MANAGER
Live your purpose and make a difference with Grupo PiSA. With over 80 years of history, Grupo PiSA is a 100% Mexican company committed to the health and well-being of millions of people, both in Mexico and internationally. Our growth reflects the effort, passion, and dedication of a team focused on excellence. Join us and become part of a company where every day is an opportunity to live "A Life in Service of Life". Together we can transform the future of healthcare and leave a positive mark on the world! Ensure regulatory compliance for activities related to purchasing, production, packaging, analysis, validation, storage, and distribution of products carried out at the plant, in accordance with the master documents of the Quality Management System, and define the strategy for executing activities within the Compliance, Operations, and Quality Control departments. **1\.** **Main job responsibilities:** * Ensure that authorized operating procedures under their responsibility are aligned with applicable regulatory requirements, corporate policies and directives, as well as Good Manufacturing Practices, and ensure these remain current during operations. * Establish controls and verify the integrity of information and data generated in the documentary chain of systems that are part of their responsibilities. * Ensure proper retention of documents related to drug manufacturing in accordance with current regulations and, when applicable, international regulations (manufacturing records, analytical records, raw material records, logbooks). * Ensure that all areas of the quality control laboratory involved in the analysis of raw materials (active and excipients), bulk products, and finished products perform testing using previously validated or verified (when applicable) analytical methods, current reagents, certified or suitable laboratory supplies, qualified and/or calibrated equipment, specifications aligned with the authorized conditions of the health registration for each product, and using approved monographs aligned with relevant Pharmacopoeias. * Lead appropriate investigations within their laboratory units for Out-of-Specification (OOS) results to identify root causes, conducting investigations requiring expanded sampling plans. 2\. **Education level:** * Bachelor's degree in chemical sciences: Pharmacy & Biochemistry, Chemical Engineering, Food Science or related field (Degree and professional license) 3\. **Experience:** * Pharmaceutical industry (Mandatory) 4\. **Knowledge:** * FDA: 12 CFR 21, 210 and 211 * Investigating Out-of-Specification (OOS) * Test Results for Pharmaceutical Production Guidance for Industry Guideline * ICH: Q1A-Q1F, Q2, Q3A-Q3E, Q6, Q10, Q14 * EMA At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE of charge; report any irregularities at lineaeticagrupopisa@letica.email Job type: Full-time Benefits: * Company car * Discounts and preferential prices * Company parking * Medical expense insurance * Cafeteria service * Company phone * Grocery vouchers Workplace: On-site
FG26+G5 La Teja, Jal., Mexico
Negotiable Salary
ANALYST FOR DEVELOPMENT AND VALIDATION OF METHODS63843585861891122
Indeed
ANALYST FOR DEVELOPMENT AND VALIDATION OF METHODS
For over 80 years, we have been providing medications, products, and services to public and private sectors in the most important healthcare markets in Mexico and Latin America. We have more than 15,000 professionals and employees committed to contributing to the preservation of the most valuable asset for everyone, our life! OBJECTIVE: Perform development, validation, and transfer analysis of analytical methods in compliance with regulatory requirements and established programs, to ensure the quality of New Products (NP), Reformulations (RF), products and materials, properly documenting results in order to meet the objectives set by the Business Unit. ACTIVITIES: · Carry out activities related to the Quality System under a code of compliance with Good Manufacturing Practices (GMP) · Develop and/or validate analytical methods ensuring compliance with current regulations, both for active ingredients, excipients, products, New Products (NP), and Reformulations (RF). · Perform analytical transfer of validated and/or verified methods to comply with current regulations for active ingredients, excipients, development products for New Products (NP), and Reformulations (RF). REQUIREMENTS: · Bachelor's degree (Bachelor's degrees in chemical areas QFB\-Pharmacy, Chemical Engineering, Food Engineering or related fields.) · Certificate of completion of studies EXPERIENCE: · Pharmaceutical industry · Validation and transfer of analytical methods · Gas chromatography KNOWLEDGE: · NOM 059 (Good documentation practices, storage, etc.) · NOM\-059, NOM\-073, good laboratory practices · Statistical process analysis WE OFFER: · Direct hiring · Permanent position based on performance · Benefits exceeding legal requirements Recruitment, evaluation, interview, selection, and hiring processes are completely FREE of charge at Grupo PiSA; no one should request any payment from you to participate in our Recruitment and Selection processes Job type: Full-time Salary: $1\.00 \- $2\.00 per month Benefits: * Savings fund * Free parking * Life insurance * Cafeteria service * Free uniforms * Grocery vouchers Work schedule: * Rotating * 12-hour shift Application question(s): * Have you used trace methodologies? * What experience do you have in developing and/or validating methodologies? Work location: On-site job
FG26+G5 La Teja, Jal., Mexico
MXN 1-2/hour
ANALYST DEVELOPMENT AND METHODS VALIDATION63843583781123123
Indeed
ANALYST DEVELOPMENT AND METHODS VALIDATION
Live your purpose and make a difference with Grupo PiSA. With more than 80 years of history, Grupo PiSA is a 100% Mexican company committed to the health and well-being of millions of people, both in Mexico and internationally. Our growth reflects the effort, passion, and dedication of a team focused on excellence. Join us and become part of a company where every day is an opportunity to live "A Life in Service of Life". Together we can transform the future of health and leave a positive mark on the world! **Position Objective** Execute the Validation and maintenance of the Validated State of physicochemical analytical methods that need to be implemented and/or used for the evaluation of inputs and products, at any of their stages: Design, Qualification, and Maintenance **Responsibilities and activities** * Conduct activities associated with the Quality System under a compliance code to GMP. * Carry out the design of analytical methods (stage 1\). * Carry out the performance qualification of analytical methods (stage 2\). * Carry out the maintenance of the validated state of analytical methods (stage 3\). **Experience** * Chromatographic analysis (liquids and gases) * Mass spectrometry analysis * Dissolution analysis and dissolution profiles * Handling of analytical instruments in the pharmaceutical sector * Development and validation of analytical methods **Knowledge** National and international pharmacopoeias Good Laboratory Practices (GLP), Good Documentation Practices (GDP) Regulatory standards (COFEPRIS, FDA, ICH, EMA or NOMs) **Education** Bachelor's degree in Pharmaceutical Chemistry, Chemistry, Chemical Engineering or related field **Complementary Profile** Proof of completion of studies (Carta Pasante) required. Availability to work rotating shifts. At Grupo PiSA, we prohibit violence and discrimination, promoting equal opportunities, inclusion, and diversity. Our selection processes are FREE; report any irregularities at lineaeticagrupopisa@letica.email Job type: Full-time, Indefinite term Salary: $15,000.00 \- $23,000.00 per month Benefits: * Savings fund * Employee discounts * Discounts and preferential prices * Life insurance * Subsidized cafeteria service * Grocery vouchers Application question(s): * Do you have experience in HPLC? Work location: On-site
G99J+6Q San Isidro Mazatepec, Jal., Mexico
MXN 15,000-23,000/year
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