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German-Speaking Pharmaceutical Industry Engineer - Casablanca

Company sector : Other services

Published today on ReKrute.com
  • 1 job(s) in Casablanca and region - Morocco
  • COMPANY :

    Capgemini Engineering is the brand of the Capgemini group that brings together the engineering and R&D services of Altran, a world leader in the sector that Capgemini finalized the acquisition of in 2020, and Capgemini's expertise in digital manufacturing. Thanks to in-depth sector knowledge and mastery of cutting-edge digital and software technologies, Capgemini Engineering supports the convergence of the physical and digital worlds. Combined with the Group's full capabilities, it helps companies accelerate their transformation towards Intelligent Industry. Capgemini Engineering has more than 52,000 engineers and scientists in over 30 countries, in sectors such as aerospace, automotive, rail, communications, energy, life sciences, semiconductors, software and the Internet, space and defense, and consumer goods.

    Capgemini Engineering is part of the Capgemini Group, a global, responsible, and multicultural leader, bringing together 300,000 people in nearly 50 countries. A strategic partner for companies in transforming their business by leveraging the full power of technology, the Group is guided daily by its purpose: to unleash human energy through technology for an inclusive and sustainable future. With over 50 years of experience and strong expertise in various business sectors, Capgemini is recognized by its clients for meeting all their needs, from strategy and design to operations management, by leveraging innovations in the ever-evolving fields of cloud, data, Artificial Intelligence, connectivity, software, digital engineering, and platforms. The Group generated revenue of 16 billion euros in 2020.

    Get the Future You Want* - www.capgemini.com.


    Company culture :

    Capgemini Engineering is characterized by a strong collaborative culture, placing people, trust and teamwork at the core of its operations. A close management approach supports guidance, empowerment and talent development within a caring environment. This dynamic is reinforced by a significant innovation dimension, encouraging creativity, initiative and experimentation to deliver high-value solutions. It is also supported by a structured organizational foundation ensuring rigor and reliability, while a more moderate competitive component sustains a balanced performance mindset.

    Job :

    As part of strengthening our Quality activities, we are looking for a CQR Engineer with 3 to 5 years of experience in a pharmaceutical environment. You will play a key role in implementing and monitoring Commissioning, Qualification, and Validation (CQV) activities to ensure that equipment, processes, and documentation comply with regulatory requirements and current quality standards.
    You will work with multidisciplinary teams and actively participate in the continuous improvement of quality systems in a demanding and regulated environment.

    Daily tasks involve various technical missions aimed at operational excellence:

    • Plan, coordinate, and carry out Commissioning, Qualification, and Validation (IQ/OQ/PQ) activities for laboratory and production equipment.
    • Write, review, and approve qualification/validation protocols and reports in accordance with GMP, FDA, ICH requirements, and other applicable standards.
    • Ensure document management related to qualification and validation activities.
    • Evaluate and handle deviations, change controls, and impact analyses, ensuring regulatory compliance is maintained.

    Required profile :

    The ideal candidate holds a Master's degree / Engineer's degree, preferably in Quality, Pharmacy, Biology, Chemistry, Process Engineering, or equivalent.

    Mastery of highly regulated environments is key to success. Expected skills include:

    • 3 to 5 years of experience in the pharmaceutical industry, preferably specializing in Qualification & Validation (CQV).
    • Good command of GMP, GLP, FDA, ICH standards and the sector's regulatory requirements.
    • Knowledge of sterile environments and processes is a major asset.
    • Excellent analytical, organizational, and document management skills.
    • Ability to work in a team and communicate with various stakeholders.
    • Fluent English and German, both written and spoken.

    If this challenge matches your professional aspirations, send your CV to the recruiter now to join a demanding and stimulating organization.

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