PpPharmaprogress is a reliable Contract Research Organization part of the Kymos Group, a fast growig company with a strong commitment to quality and a dedication to innovation. Our customers have acceess 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. /p pWe are looking for a bFinished Products Testing /b bScientist /b to ensure the correct development of assigned analytical projects. /p pbThe responsibilities of the position include: /b /p ul liDesign, supervise, and execute quality control testing of finished products /li liManage assigned projects, keeping deadlines and establishing direct communication with clients. /li liWrite technical documents associated with studies (protocols, reports, standard procedures, certificates of analysis). /li liDirect and supervise the experimental work of technical staff. /li liPerform the work in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). /li /ul pbKymos 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. /b /p h3Requirements /h3 ul liBachelor’s degree in chemical or Biochemical Sciences. /li liKnowledge of HPLC and GC techniques, with an understanding of analytical development departments. /li liGood knowledge of method development with liquid chromatography coupled to mass spectrometry techniques /li liExperience in managing technical documents associated with studies (standard procedures, certificates of analysis, deviations, OOSs, CAPAs, etc.). /li liExperience working in GMP environments is required. /li liExperience in similar roles in the pharmaceutical industry. /li liDetail-oriented and able to achieve objectives. /li /ul pbSector: /b Pharmaceutical and biopharmaceutical /p /p #J-18808-Ljbffr