Position Summary: Coordinate, organize, and verify the work of personnel under supervision in projects involving the development, validation, and execution of analytical techniques for quantifying analytes in dissolution profile samples. Key Highlights: 1. Leadership and team management in pharmaceutical scientific research. 2. Ensuring compliance with Good Laboratory Practices and Documentation. 3. Implementation of improvements in analytical development. *Do you enjoy rigorously analyzing scientific evidence while also communicating clearly and ethically?* At Grupo CINASI–UNEBI, a company specialized in pharmaceutical scientific research, we conduct bioequivalence, bioavailability, and biopharmaceutical evaluation studies adhering to high regulatory and scientific standards. ***Position: Chemist for Dissolution Profiles*** ***Location:*** *C. 9 171, Residencial La Soledad, 45525 San Pedro Tlaquepaque* **Position Purpose** Coordinate, organize, and verify the work of personnel under supervision in projects involving the development, validation, and execution of analytical techniques for quantifying analytes in dissolution profile samples. **Main Responsibilities** * **Project Management:** Collaborate with the Laboratory Head to establish strategies ensuring timely and effective achievement of objectives; develop detailed scheduling for area projects. * **Technical Supervision:** Review validation reports, study protocols, and analytical procedures. Approve results obtained from drug quantification. * **Regulatory Compliance:** Ensure all processes are conducted under **Good Laboratory Practices and Documentation**, maintaining data integrity (Data Integrity). * **Process Optimization:** Implement new conditions representing improvements to analytical development and issue work plans for method validation. * **Talent Management:** Lead, advise, and evaluate supervised personnel (analytical chemists and technicians); coordinate onboarding training and propose career development plans. * **Quality Maintenance:** Update quality management system procedures based on current regulations and international accreditation bodies. **Required Profile** * **Academic Qualification:** Completed bachelor’s degree (degree certificate mandatory) in Chemical-Biological or Pharmaceutical Chemistry fields. * **Experience:** 2 to 5 years in similar roles within the pharmaceutical sector or research laboratories. * **Essential Technical Knowledge:** * Proficiency in **HPLC and LCMS** chromatography. * Development of bioanalytical methods and validation statistics. * Knowledge of **NOM-177-SSA1-2013**, ICH Q2, OECD, and FDA guidelines. * Compliance with **CFR 21 Part 11**, pharmacokinetics, and bioequivalence. * Familiarity with NMX-EC-17025-IMNC and Audit Trail processes. * **Digital Tools:** Microsoft Office and specialized software for chromatographic equipment. **Competencies and Skills** * Leadership and team management. * Results-oriented mindset and continuous improvement focus. * Strong analytical ability and risk prevention capacity. * Effective communication and autonomous work under guidance. **We Offer** * Salary negotiable based on experience and profile. * Monthly food vouchers. * Biweekly payroll. * Statutory benefits from day one. * Birthday leave. * Financial support for psychological consultations. * Scheduled vacations. * Continuous training, development plans, and growth opportunities. ***Why Join Grupo CINASI–UNEBI?*** *Because we believe scientific excellence is measured not only in data but also in the responsibility with which we impact public health. Here, technical rigor, professional ethics, and human experience go hand-in-hand to ensure safe, effective, and high-quality medicines.* Employment Type: Full-time Salary: $17,000.00 \- $20,000.00 per month Benefits: * Discounts and preferential pricing * Option for indefinite-term contract * Additional vacation days or paid leave * Food vouchers Workplace: On-site employment