Validación Métodos Analitíco

buscojobs Argentina; Chubut; Presencial; ARS 66.470.000 - 93.060.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking an Analytical Method Validation Specialist. The ideal candidate will perform method validation analyses, execute tests according to established protocols, and ensure compliance with GMP standards. Join a multicultural company focused on collaboration and innovation, offering opportunities in international projects and personal development.

Formación

• Experience in the pharmaceutical industry, specifically in method validation.
• Ability to execute validation tests and document all analyses.
• Familiarity with GMP standards and laboratory equipment.

Responsabilidades

• Perform analytical method validation analyses.
• Execute validation tests as required by the protocol.
• Document all analyses performed, in compliance with GMP standards.

Conocimientos

Physicochemical analysis of finished products

Physicochemical Analytical Method Validations

Laboratory equipment handling (HPLC, UPLC, UV, IR, KF)

Knowledge of GMP standards

Descripción del empleo

Get AI-powered advice on this job and more exclusive features.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.

Due to our continuous growth, PQE Group is seeking an Analytical Method Validation Specialist with experience in the pharmaceutical industry.

Required Profile

General Responsibilities:

Perform analytical method validation analyses in accordance with established validation protocols, following current SOPs and company policies.

Tasks:

• Execute validation tests as required by the protocol
• Issue documentation, including validation protocols and reports
• Receive and properly store samples for analysis
• Fully document all analyses performed, in compliance with GMP standards and regulatory requirements
• Maintain proper organization and cleanliness in the laboratory
• Properly use laboratory equipment and keep equipment logs up to date

Knowledge:

• Experience in physicochemical analysis of finished products (tablets and suspensions)
• Experience in Physicochemical Analytical Method Validations
• Experience handling laboratory equipment: HPLC, UPLC, UV, IR, KF
• Knowledge of GMP standards, processes, and continuous improvement

Next Steps

Upon receiving your application, the recruiting department will contact you for an initial HR interview if your profile matches. Successful candidates will proceed to a technical interview with the Hiring Manager. Final steps include further discussions or feedback based on interview outcomes.

Working at PQE Group

As part of PQE, you will join a challenging, multicultural company that values collaboration and innovation. PQE offers opportunities to work on international projects, develop your skills, and collaborate with colleagues worldwide.

If you seek a rewarding and exciting career, PQE Group is the ideal place for you.

Apply now and take the first step towards an amazing future with us.

Seniority level

Associate

Employment type

Full-time

Job function

Consulting

Industries

Pharmaceutical Manufacturing