QC Chemical Analyst — Impactful GMP Lab Roles (Shifts)

BSP Pharmaceuticals S.r.l.; Mostacciano; Hybrid; EUR 35,000 - 52,000; Full time

Job summary

BSP Pharmaceuticals S.p.A. is a CDMO providing development and manufacturing for cytotoxic and non-cytotoxic therapies.

We are currently looking for a QC Chemical Analyst who will mainly ensure chemical analysis of materials and products, and daily use of main laboratory equipment like HPLC, UPLC, UV, KF and IR. You will draft GMP documentation, handle reagents and data software such as Empower, Totalchrom, UV WinLab ES, Excel and LIMS, and work on shifts with GMP knowledge and English

Qualifications

• MA degree in Chemistry or equivalent.
• At least 2 years in similar analytical roles in complex organizations.
• Knowledge of GMP and working in shifts.
• English working knowledge.

Responsibilities

• Chemical analysis of raw materials, semi-finished and finished products.
• Daily use and control of lab equipment (HPLC, UPLC, UV, KF, IR).
• Manage capillary electrophoresis and evaluate results.
• Draft GMP documentation and handle reagents and standards.
• Use Empower, Totalchrom, UV WinLab ES, Excel and LIMS for data.

Skills

Analytical chemistry

Quality control

English proficiency

Education

MA degree in Chemistry

Tools

HPLC

UPLC

UV

KF

IR

Capillary electrophoresis

Empower

Totalchrom

UV WinLab ES

Excel

LIMS

Job description

BSP Pharmaceuticals S.p.A. is a CDMO providing development and manufacturing for cytotoxic and non-cytotoxic therapies.

We are currently looking for a QC Chemical Analyst who will mainly ensure chemical analysis of materials and products, and daily use of main laboratory equipment like HPLC, UPLC, UV, KF and IR. You will draft GMP documentation, handle reagents and data software such as Empower, Totalchrom, UV WinLab ES, Excel and LIMS, and work on shifts with GMP knowledge and English