Quality Control and Technology Transfer Expert

Quality Control and Technology Transfer Expert

Devire

Lokalizacja
Warszawa
HPLC
GC
TLC
walidacja metod analitycznych
GMP

Hexjobs Insights

Zatrudniony na stanowisku Eksperta ds. Kontroli Jakości i Transferu Technologii będzie wspierał projekty rozwojowe w międzynarodowej firmie farmaceutycznej z Warszawy.

Słowa kluczowe

HPLC
GC
TLC
walidacja metod analitycznych
GMP

Benefity

  • Prywatna opieka medyczna i stomatologiczna
  • Ubezpieczenie na życie
  • Współfinansowanie karty sportowej
  • Szkolenia wewnętrzne i zewnętrzne

Your future companyWe are partnering with a leading pharmaceutical company that specializes in drug manufacturing, wholesale distribution, and provides transportation as well as research and development services.As part of their continued growth, we are seeking a Quality Control and Technology Transfer Expert to join their team. This is an exciting opportunity to work in a dynamic environment focused on innovation and excellence in the pharmaceutical sector.RequirementsAt least 2 years of experience in quality control (HPLC, GC, TLC) within the pharmaceutical industry,Ability to communicate clearly and respectfully at all levels, consistently advocate for your objectives, and drive topics forward with commitment and determination,University degree in pharmaceutical sciences, chemistry, or a related scientific discipline,Experience in technology transfers and analytical method validation,Creative mindset with the ability to think outside the box and challenge current CMC development strategies,Ability to identify and solve critical problems,Strong team player with excellent interpersonal and communication skills,Willingness to travel and work within a remote, international team environment,Knowledge of GMP requirements,Very good knowledge of English.ResponsibilitiesSupport current and new development projects at the CMO,Assist in implementing and maintaining production processes and quality control testing,Perform quality control testing (HPLC, GC, TLC),Prepare, write, and update GMP documentation,Track and report the progress of projects,Participate in regular internal project meetings to discuss and plan activities,Participate in regular meetings with contract organizations to provide project updates via teleconference or on-site visits, as appropriate,Maintain records documenting all relevant communications related to projects,Monitor project timelines and contracts for accuracy and follow up on any discrepancies with stakeholders,Collaborate closely with other departments within the organization to ensure alignment and effective communication across all project areas.The offerAn interesting opportunity for further development within international company,Private medical and dental care,Life insurance,Co-financing of sport card,Internal and external training.

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Opublikowanadzień temu
Wygasaza około 22 godziny
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