quality assurance gmp (good manufacturing practice) specialist

☞ Randstad

Ver: 135

Dia de atualização: 26-11-2025

Localização: Braine-l’Alleud Walloon Brabant

Categoria: Marketing / PR

Indústria:

Tipo de empregos: Freelance

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Conteúdo do emprego

job details

summary

  • braine-l’alleud
  • contract
  • 40 hours per week
  • group function
    technics
  • reference
    CXRSP-108545
job details

We are looking for a Quality Assurance GMP (Good Manufacturing Practice) Specialist for one of our clients based in Braine-l’Alleud.

Don’t hesitate to contact me: siham.haddouchi@professionals.randstad.be

...

We are looking for a Quality Assurance GMP (Good Manufacturing Practice) Specialist for one of our clients based in Braine-l’Alleud.

Don’t hesitate to contact me: siham.haddouchi@professionals.randstad.be

  • key responsibilities

    The QA/QP:

    • Ensures that operations in relation to imported or manufactured raw materials and bulk pharmaceutical products comply with national and/or international regulations and guidelines (cGMP) as well as the company’s quality policies.

    • Ensures that products comply with the relevant marketing dossiers.

    • Takes decisions on the release, rejection or re-working of these products.

    • Proactively assists operations in identifying, developing and implementing quality and operational excellence improvements in response to business, technical and regulatory requirements.

    As a QA/QP, your main responsibilities will include:

    • Release and certification of the above mentioned product batches, management of legal samples.

    • Management of quality deviations, investigations, CAPAs, market/customer complaints, recalls, temporary and permanent change controls.

    • Drafting, review and approval of Product Quality Reviews.

    • Drafting, review and approval of procedures related to the field of activity.

    • Follow-up and QA support to projects defined by the QA management, and more specifically in relation to the release and production activities of dry forms.

    • Carrying out internal audits, participating in customer audits and inspections in relation to the field of activity.

  • qualifications

    For this assignment we are looking for the following qualifications and skills:

    • Degree in Industrial Pharmacy with Qualified Person (QP) number.

    • Experience in the pharmaceutical GMP environment in a similar position, and/or experience in Quality Assurance, Production or Quality Control

    • Knowledge of international regulations related to GMP activities.

    • Very good knowledge of French and English (spoken and written).

    Soft skills :

    • Able to take decisions based on facts and to take responsibility for them.

    • Sense of discretion and ethics.

    • Highly developed team spirit, excellent interpersonal skills, including oral and written communication.

    • Resistant to stress.

    • Ability to solve problems and provide constructive and innovative solutions.

  • key benefits

    Consultancy

    We offer an attractive salary with extra-legal advantages:

    • Group insurance

    • Hospitalisation insurance

    • Meal vouchers of 7 euros gross per working day

    • Reimbursement km or company car

    • Monthly allowance (80 euros net per month)

    • A 13th month

    • Training

    • Etc.

    A rate as a freelancer is also possible.

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Data limite: 10-01-2026

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