Piramal Pharma Solutions
Héctor Almanza has extensive experience in quality and regulatory affairs in the pharmaceutical industry. Héctor Almanza currently serves as the Director of Quality and Regulatory Affairs at Piramal Pharma Solutions, where they oversee departments such as Quality Assurance, Quality Control, Analytical Services, and Regulatory Affairs. Héctor Almanza specializes in data integrity and has dealt with regulatory inspections from various agencies such as FDA, EMA, and EDQM.
Prior to their current role, Almanza worked as the Quality Director and Qualified Person at Dr. Reddy's Laboratories, where they were responsible for the Quality Assurance and Quality Control departments. Héctor Almanza also gained experience in regulatory inspections and data integrity during their time at this company.
Before joining Dr. Reddy's Laboratories, Almanza worked at Laboratorios Liomont as a Quality Assurance Manager, focusing on the implementation and maintenance of the Quality Management System based on ISO 9001. Héctor Almanza had responsibilities in product release, documentation, process inspection, approval of raw materials, customer complaints, and audits.
Almanza's earlier experience includes working as a Quality Assurance Manager at Teva Active Pharmaceutical Ingredients, where they held the same position for Baxter International Inc. In these roles, they were involved in managing pharmaceutical critical systems, continuous improvement, documentation systems, operational quality supervision, audits supervision, and quality auditing.
Overall, Almanza's work experience demonstrates their expertise in quality assurance, quality control, regulatory affairs, and data integrity, making him a reliable professional in the pharmaceutical industry.
Héctor Almanza Quality and Regulatory Affairs Director completed their education at Universidad Nacional Autónoma de México from 2019 to 2021, where they obtained a specialization in Industrial Pharmacy, focusing on pharmacy, pharmaceutical sciences, pharmacology, and administration. Prior to that, they obtained a Bachelor's degree in Chemical Engineering from the Universidad de Guanajuato from 1989 to 1994.
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Piramal Pharma Solutions
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Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug product. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovator and generic companies worldwide.