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Teuta Gashi

Experienced scientist in the pharmaceutical industry. (10+ years)

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ZugMitglied seit 1. Juni 2026
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Über

Experienced scientist in the pharmaceutical industry with 10+ years of experience. Management experience as Project Manager, Project leader, Order Manager, SPOC. Currently pursuing Master of Science in Sustainable Chemistry (4th Semester).

Berufserfahrung

Project Manager Planning - Carbogen Amcis AG

(2025-05)

  • Responsible for Proposals (Production and Analytical part)
  • Resource Planning at all Sites by using MS Projects and customized internal tool
  • Process Improvement
  • Planning customer Visiting

Analytical project coordinator - Carbogen Amcis AG

(2023-04 - 2025-04)

  • Analytical project management and leading a project team on behalf of internal and external global clients
  • Responsibility for the coordination of analytical project activities at various locations
  • SPOC to internal and external clients
  • Strategic coordination of sub-projects within a client program
  • Project controlling and budget responsibility to ensure economic viability
  • Technical decisions, prioritization and support of employees in the group in method development, optimization, validation, identification and tracking of secondary components and impurities as well as technical troubleshooting

Senior Quality Control specialist und LIMS Administrator - B. Braun Medical AG

(2021-04 - 2023-03)

  • Batch Record Review, Preparation/adaption of SOPs, Changes, Deviations, OOS/OOT/OOE, Complaints
  • Project Manager

Project leader and SPOC - Solvias AG/Kaiseraugst

(2014-10 - 2021-03)

  • Designs, plans, performs, interprets and reports results of scientific experiments for the preparation and timely delivery of drug substances (DS) and drug products (DP)
  • Recruitment of new scientists and project leaders
  • Analytical support, order manager and supervision of process validation, verification, method transfer, in-use studies, stability studies
  • Support of global key accounts, relationship management of international clients
  • Project leader and single point of contact (SPOC)
  • Close collaboration with other sections within Solvias, sample management team, sales department and quality assurance
  • Development of quotations
  • Plan and coordinate the laboratory resources under GMP-guidelines
  • Review of raw data (generated in 8 labs)
  • Author and reviewer of validation and stability plans and reports
  • Release of analytical reports and CoA's
  • Analytical support and supervision of method transfer, verification, stability studies
  • Handling of OOS, OOE and OOT-cases
  • LIMS power user (issuing and modifying LIMS tests), Product specifications
  • Responsible for JARE (Jahresrechnung), and applications of import authorizations at Swissmedic for narcotic substances, including audits
  • Handling Deviations (CAPAs, risk assessments), Changes and customer complaints
  • Deputy of team leaders

Ausbildung

College - Technical, mathematical and scientific studies - University of Johannes Gutenberg in Mainz, Germany (2001 - 2002)

Chemistry - Biomedical Chemistry - University (2002 - 2009)

PhD - Analytics and Inorganic Chemistry - University (2010 - 2013)

Master of Science - Sustainable Chemistry - Leuphana University in Lüneburg (2024)

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