Opis pracovnej ponuky

We are looking for a motivated Industrial Pharmacist / Qualified Person to ensure the release of batches of pharmaceutical products. The ideal candidate will be responsible for quality assurance and regulatory compliance, ensuring that products meet the highest standards of quality and safety before they are released to the market.

As an ALTEN consultant, you will have the opportunity to be part of the following activities:

  • Ensure the release of batches of pharmaceutical products in accordance with local and international regulations
  • Act as the quality assurance representative to approve production activities and associated documentation
  • Perform critical reviews of batch records, including certificates of analysis, manufacturing and control protocols, and test reports
  • Work closely with production, quality control, and pharmaceutical development teams to ensure the quality of pharmaceutical products
  • Ensure that facilities, equipment, processes, and procedures are in compliance with quality and safety standards
  • Participate in incident, deviation, and change management, and conduct quality investigations
  • Maintain a thorough knowledge of local and international regulations related to batch release and regulatory compliance

If you see yourself in this position, then you are the one we are looking for! Do not hesitate to send your CV to our recruitment team on apply@alten.be

Požiadavky na pracovné miesto
  • Master’s degree in pharmacy or a related field
  • Qualified Person (QP) certification in compliance with local and international requirements, or in the process of obtaining it
  • No minimum professional experience requirement outside of the internship for obtaining the QP number
  • Excellent written and verbal communication skills to interact with team members, customers, and business partners
  • Ability to work independently and as part of a team to solve problems and achieve quality and regulatory compliance goals
  • Strong analytical and problem-solving skills, with particular attention to detail
  • Thorough knowledge of local and international regulations related to batch release and regulatory compliance
  • Knowledge of quality standards and regulatory compliance procedures for pharmaceutical product manufacturing
Pracovné obmedzenia

mandatory GMP experience under FDA or EMA norms 

Podrobné informácie o pracovnom mieste
Odvetvie:
Other service activities
Oblasť zamestnania:
Engineering professionals (excluding electrotechnology)
Ponúka:
Engineering and engineering trades, Life sciences, Manufacturing and processing
Pracovné skúsenosti:
Work experience is required
Oblasť vzdelania:
Between 2 and 5 years
Jazykové zručnosti:
  • Dutch
  • Fluent
  • English
  • Fluent
  • French
  • Fluent
Required skills:
apply GMP, apply knowledge of science, technology and engineering, evaluate pharmaceutical manufacturing process
Platové rozpätie (Mesačne):
2500 - 5000 EUR (Gross pay)
Date of expiry:

About organisation

ALTEN Belgium is a leading consultancy company in the fields of Engineering, Life Sciences and IT in which our people and clients are central. In our open and adaptable organization, we get the best out of our ambitious employees enabling them to perform optimally. We do this by offering them the most challenging projects, but also to continuously acquire new expertise to boost their careers… Find out more

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