QC Chemistry Analyst – Biotech GMP Quality & Growth

GRIFOLS, S.A.

Dublin

Presencial

EUR 45.000 - 65.000

Jornada completa

Hace 4 días
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Ventajas ofrecidas por este puesto de trabajo

Competitive salary package
Group pension scheme
Private medical insurance
Career development opportunities
Succession planning

Descripción de la vacante

Grifols Worldwide Operations (GWWO) is seeking a QC Chemistry Analyst to support purification and aseptic manufacturing in a state-of-the-art facility. You will report to the QC Chemistry Supervisor and enjoy strong career development opportunities within a global biotechnology company.

You will perform raw material, in-process and finished product analyses using HPLC, spectrophotometry and related techniques, participate in method transfer and validation, and ensure compliance with cGMP.

Formación

  • Bachelor’s degree in Chemistry or Biochemistry.
  • Minimum of 2 years of related experience.
  • Knowledge of analytical techniques/instruments including HPLC and spectrophotometry.
  • Experience with biologics or protein-based therapeutics is desirable.

Responsabilidades

  • Carry out raw material, in-process and finished product chemistry and immunochemistry analysis.
  • In-process and finished product QC including protein and excipient analysis using analytical techniques (HPLC, Spectrophotometry, etc.).
  • Raw material QC including Karl-Fischer, FT-IR and NIR techniques.
  • Ensure laboratory processes, equipment and services are installed, qualified and maintained appropriately.
  • Participate in verification, validation and technical transfer of analytical testing procedures.
  • Ensure adherence to cGMP and company specifications.

Conocimientos

Chemistry
Biochemistry
Analytical thinking
Verbal communication
Team collaboration
Problem-solving

Educación

Bachelor’s degree in Chemistry/Biochemistry

Herramientas

HPLC
Spectrophotometry
Electrophoresis
Karl-Fischer
FT-IR
NIR
GC
Flame-photometry
AA

Descripción del empleo

Grifols Worldwide Operations (GWWO) is seeking a QC Chemistry Analyst to support purification and aseptic manufacturing in a state-of-the-art facility. You will report to the QC Chemistry Supervisor and enjoy strong career development opportunities within a global biotechnology company.

You will perform raw material, in-process and finished product analyses using HPLC, spectrophotometry and related techniques, participate in method transfer and validation, and ensure compliance with cGMP.

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