Analytical Development Senior Scientist Mass Spectrometry

Posted 13 Hours Ago
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Athens
Senior level
Software • Pharmaceutical
The Role
The Analytical Development Senior Scientist is responsible for conducting protein analysis using Mass Spectrometry and chromatography methods. Duties include method development, data interpretation, regulatory documentation, and collaborating with Quality Assurance. The role also involves facilitating internal training and maintaining analytical infrastructure in line with EU and US regulations for biotech product development.
Summary Generated by Built In

Description

At DEMO SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are excited to kick-off our Biotechnology project in Athens.

The field of Biotechnology is bringing about fascinating developments in medicine, treatments, and healthcare, as new, effective medicines are being produced from extremely complex natural compounds, with a biological origin. Demo leads the way in the Greek pharmaceutical market with major investments in Biotechnology

  • We are building a prototype unit for the development of monoclonal antibodies
  • We are creating a contemporary Research and Development Center for biotechnology
  • We are starting research for three finished pharmaceutical products with monoclonal antibodies
  • We are establishing a Biotechnology Academy to train young scientists. Biotechnology is becoming part of our lives.

As a result, we are currently looking for a high caliber Analytical Development Senior Scientist Mass Spectrometry:

Main duties and responsibilities:

  • Conduct protein analysis with use of Mass Spectrometry based methods, e.g peptide mapping, disulphide bridges mapping, post translational modifications, intact mass profiling etc.; and chromatography methods
    • Analytical methods development and qualification,
    • Data interpretation and reports writing,
    • Trouble shooting,
    • Regulatory documentation writing, review and editing.
    • Support of Process development by providing the analytical data,
    • Document writing such as SOP, Protocols and reports
    • Analytical methods transfer to QC
  • Facilitate internal trainings to Bio-team colleagues
  • Contribute to development projects by:

-Follow and implement EU and US regulations regarding all aspects related to the quality and analytical characterisation of biological medicinal products with an emphasis on biosimilars development

-Setup and maintenance of the analytical infrastructure required for AD with emphasis to Mass Spectrometry

  • Collaboration with Quality Assurance dept. to set up and supervision the quality system required to run Analytical Development and QC depts
Requirements

Experience, skills and qualifications required:

  • Bachelor’s Degree in Biology, Biotechnology, Chemistry or related with post graduate studies (MSc / PhD) in a field related to biotechnology, biochemistry or molecular biology
  • Minimum 5 years of experience in biotech/biosimilar or pharmaceutical company in the field of biotech
  • Good understanding of regulations required for analytical development of biotech products, preferably in biosimilars development
  • Working experience in method development and validation of common pharmaceutical analytical techniques such as : Mass Spectrometers, UPLC, FTIR, CD, Capillary Electrophoresis
  • Very good knowledge of software like: Empower, Data visualization and statistics like: Graph Pad Prism, JASP, JMP or similar
  • Working experience in analytical techniques for protein analysis regarding their physical-chemical structure with emphasis to mass spectrometry and chromatography
  • Strong problem solving attitude, critical thinking
  • Resilience & ability to work independently
  • Excellent communication skills both verbal and written
  • Team player & fast learners
Benefits

The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.

All applications will be considered as strictly confidential.

Top Skills

Mass Spectrometry
The Company
HQ: Krioneri
849 Employees
On-site Workplace

What We Do

DEMO is a dynamic Greek industrial and commercial organization, specializing in the development, production and supply of pharmaceutical products.
The company is the largest supplier of injectables for public hospitals in Greece, exports 80% of its annual production and is recognized as one of the official suppliers of the United Nations, UNICEF, the World Health Organization (WHO), Doctors Without Borders and the International Committee of the Red Cross. With over 3,300 circulation licenses in 86 countries worldwide, the largest factory in SE Europe and over 1,400 employees, DEMO paves the way for pharmaceutical self-sufficiency for Greece and Europe.
Today, DEMO implements investments of €356 million, strengthening production and R&D, while entering the development and production of active ingredients and Biotechnology.
At the same time, the company is committed to ensuring equality, diversity and inclusion in the working environment and has adopted -within this context- the Diversity Charter for Greece.
DEMO moves "Always Forward" driven by its corporate philosophy of providing quality and reliable pharmaceutical products, for everyone.

Learn more at www.demo.gr

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