Pharma QC Production Operator - Evening Shift (GMP Lab)

Laboratorios Medicamentos Internacionales S.A; Madrid; On-site; EUR 20,000 - 32,000; Full time

Benefits offered by this job

Company pension scheme

Home office and flexible working hours

Support for charitable projects

Health and well-being

Discounts for employees

Job summary

Aristo Pharma Group is seeking a full-time laboratory analyst to join our quality control team in Madrid. You will operate Waters and Agilent HPLC systems, perform chromatography analysis, and support stability and method validation under GMP conditions.

The ideal candidate has a Higher Degree in Laboratory Analysis and Control, intermediate English, and at least 6 months' experience in pharma QC labs. The role offers shift options and a benefits package.

Qualifications

• Higher Degree (FP II or equivalent) in Laboratory Analysis and Control.
• Proficiency in office automation and statistical analysis systems.
• Intermediate level of English.

Responsibilities

• Handling Waters and Agilent HPLC systems and UPLC with Empower software.
• Theoretical and practical knowledge of chromatographic techniques including liquid/gas chromatography, ion chromatography, spectrophotometry and potentiometric tests.
• Performing analyses for stability studies and process validation.
• Collaborating in evaluation of OOS and OOT.

Skills

HPLC

UPLC

Empower software

Waters/Agilent systems

English (Intermediate)

Education

Higher Degree in Laboratory Analysis and Control

Tools

Waters HPLC

Agilent HPLC

UPLC

Empower

Job description

Aristo Pharma Group is seeking a full-time laboratory analyst to join our quality control team in Madrid. You will operate Waters and Agilent HPLC systems, perform chromatography analysis, and support stability and method validation under GMP conditions.

The ideal candidate has a Higher Degree in Laboratory Analysis and Control, intermediate English, and at least 6 months' experience in pharma QC labs. The role offers shift options and a benefits package.