Pharmaprogress is a reliable Contract Research Organization part of the Kymos Group, a fast-growing company with a strong commitment to quality and a dedication to innovation. Our customers have access to a wide range of GMP/GLP-certified and GCP-compliant services and obtain a tailor-made, personalized, genuinely flexible service into a unique selection of services for innovative small and large molecules, generics, biosimilars, antibodies, biomarkers, ADA (anti-drug antibodies), ADC (antibody-drug conjugates), hormones, enzymes and nucleic acids.
We are looking for a Team Coordinator in the area of testing and certification of raw materials to oversee the correct development of assigned clients, projects, and staff.
ResponsibilitiesDesign and supervise analytical projects for quality control testing of raw materials.Manage and empower assigned personnel.Carry out project reports and personnel evaluations.Direct and supervise the work of the personnel in charge.Ensure compliance with GMP regulations.RequirementsProfile of the required person: Bachelor's degree in Chemical Sciences (Analytical Orientation). A Master's or Ph.D. is highly valued.Advanced knowledge of laboratory analysis techniques and quality control.Previous experience in leadership roles within the pharmaceutical industry and self-control skills.Extensive knowledge and experience in GMP environments.Demonstrated project management skills.Experience in leading work teams.Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic. Sector: Pharmaceutical and biopharmaceutical
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