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Physicochemical Laboratory Analyst

On-site in Parets del Vallès·Added 2 days ago

Manpower España

816 open roles

Overview

Job details

  • €14.52 an hour

    Gross, as stated in the ad.

Requirements

  • Have the right to work in Spain

    Manpower España doesn't mention sponsorship in the ad.

  • Work on-site in Parets del Vallès

    No relocation package mentioned.

  • Higher vocational training (FP Grado Superior)

    “Ciclo formativo de Grado superior en Análisis y Control, Laboratorio de Análisis y de Control de Calidad, o formación profesional equivalente relacionada con el ámbito de laboratorio.” — per the ad.

This job was automatically translated to English.

The role

At Manpower, we are looking for a Laboratory Analyst for an important global pharmaceutical company dedicated to manufacturing product development (CDMO), located in Parets del Vallés.

Your functions:
Register the entry of samples in Quality Control
Experience with HPLC, Spectrometry, and Chromatography analytical techniques.
Execute, register, and document the tasks performed in the Quality Control laboratories.
Investigate and document quality deviations together with the Technical staff.
Document, through the correct documentation standards (GMP), the analytical and review tasks performed.

Requirements:
- Higher Degree Vocational Training in Analysis and Control, Analysis Laboratory and Quality Control, or equivalent professional training related to the laboratory field.
- Knowledge of SAP and Office suites.
- Proficiency in analytical techniques such as HPLC, gas or liquid chromatography, Karl Fischer, UV, solutions, pH.
- Previous experience in the pharmaceutical industry is essential

We offer:
Immediate start
Schedule: Monday to Friday on a rotating shift. Morning and Afternoon (From 06:15 to 14:15 and from 13:45 to 21:45 hours)
Salary: 14.52 € gross/hour
Initial 3-month contract + possibility of continuity
At Manpower, we are looking for a Laboratory Analyst for an important global pharmaceutical company dedicated to manufacturing product development (CDMO), located in Parets del Vallés.

Your functions:
Register the entry of samples in Quality Control
Experience with HPLC, Spectrometry, and Chromatography analytical techniques.
Execute, register, and document the tasks performed in the Quality Control laboratories.
Investigate and document quality deviations together with the Technical staff.
Document, through the correct documentation standards (GMP), the analytical and review tasks performed.

Requirements:
- Higher Degree Vocational Training in Analysis and Control, Analysis Laboratory and Quality Control, or equivalent professional training related to the laboratory field.
- Knowledge of SAP and Office suites.
- Proficiency in analytical techniques such as HPLC, gas or liquid chromatography, Karl Fischer, UV, solutions, pH.
- Previous experience in the pharmaceutical industry is essential

We offer:
Immediate start
Schedule: Monday to Friday on a rotating shift. Morning and Afternoon (From 06:15 to 14:15 and from 13:45 to 21:45 hours)
Salary: 14.52 € gross/hour
Initial 3-month contract + possibility of continuity

About Manpower España

Manpower is a global workforce solutions company and a pioneer in the staffing industry, operating in over 70 countries and connecting millions of people with meaningful work each year. The company provides a wide range of services including recruitment, workforce management, and career development, serving clients across various sectors from industrial to administrative.

In Spain, Manpower has a strong presence with offices in major cities, offering local and international professionals access to a broad network of employers. The company is known for its inclusive hiring practices and support for international candidates, making it a relevant option for professionals relocating to Spain.

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