QC Chemical Analyst — HPLC/UPLC Expert, GMP, Shift Work

BSP Pharmaceuticals S.p.A.; Lazio; On-site; EUR 32,000 - 52,000; Full time

Job summary

BSP Pharmaceuticals S.p.A is a CDMO dedicated to development and manufacturing for cytotoxic and non-cytotoxic products. The QC Chemical Analyst will perform chemical analysis, operate HPLC/UPLC/U V instruments, and contribute to documentation and data integrity in a cGMP setting.

The role requires a Master’s in Chemistry, 2+ years in a similar environment, GMP knowledge, and English working proficiency. Availability for shifts is essential to support multi-site operations.

Qualifications

• Master's degree in Chemistry or related field.
• At least 2 years in a similar role within complex organizations.
• Working knowledge of GMP and English language.
• Willingness to work in shifts.

Responsibilities

• Perform chemical analysis of raw materials, intermediates and finished products per methods.
• Operate and monitor main laboratory instruments (HPLC, UPLC, UV, SoloVPE, KF, IR).
• Manage capillary electrophoresis and evaluate analytical results.
• Draft GMP documentation and maintain lab records.

Skills

Shift work

GMP knowledge

English (working)

Education

Master's 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 dedicated to development and manufacturing for cytotoxic and non-cytotoxic products. The QC Chemical Analyst will perform chemical analysis, operate HPLC/UPLC/U V instruments, and contribute to documentation and data integrity in a cGMP setting.

The role requires a Master’s in Chemistry, 2+ years in a similar environment, GMP knowledge, and English working proficiency. Availability for shifts is essential to support multi-site operations.