Qualification lab coordinator (pharma)

☞ Eurofins Belgium Digital Testing

見る: 195

更新日: 16-11-2025

場所: Lessines Hainaut

カテゴリー: IT-ソフトウェア IT-ハードウェア/ネットワーキング 情報技術 生産/操作

業界: Farmaceutisch biotechnologie

ジョブタイプ: Voltijds, Tijdelijk

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仕事内容

    Lessines, Belgium
    Full-time

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

As Qualification Lab Coordinator you are responsible to lead, support and participate to qualification and validation for new equipment to be installed in Pilot R&D area including Engineering, Maintenance & Validation tasks in compliance with Corporate and local legal requirements to support the production of Stability batches to be used in Regulatory submission file.

You have following responsibilities

  • Guarantee a state-of-the art facility in order to successfully pass various audits (QA, EHS, Corporate, etc …)
  • Independently plan, execute and direct commissioning, qualification and validation activities related to new equipment
  • Write appropriate documentation (protocols, reports, calibration and maintenance plan) in compliance with global and local requirements and procedures
  • Provide statistical relevant approach and data analysis to support validation within design space and associated risk analysis approach
  • Provide guidance for equipment validation
  • Execute validation with support of technician/operator
  • Compile reports and analysis in written and graphic form, describing observations and results
  • Directs the completion of complex projects or programs within boundaries of quality, time and budget
  • Lead and execute validation project on a cross functional basis. Using broad knowledge and experience in cross-functional activities, coordinate and direct activities of teams and individual contributors
  • Maximize the work and effectiveness of internal and external technical resources
  • Communicate adequately with other support services (IT, EHS, Facility Services, QA, Finances…)
  • Follow & improve Site Maintenance Master Plan to include new equipment needs. Create new equipment documentation such as Operating Procedure covering user procedure and maintenance plan definition
  • Propose & implement sustainability initiatives (energy reduction)
  • If needed due to lack of technical resource, support qualification operational activities

Qualifications

  • You have a Master Degree in relevant engineering discipline
  • At least 7 years of relevant work experience
  • Understanding of R&D environment, engineering and qualification-validation environment
  • Excellent knowledge of Quality Systems, GMP and GDPs requirements
  • Good project management skills
  • Demonstrated team working skills and excellent interpersonal skills
  • Stress resistant, dynamic and results driven
  • Demonstrates flexibility and can shift gears comfortably
  • Analytical mindset, sense of details
  • Fluent in French and English

Additional Information

  • Competitive salary and benefit packages
  • Training opportunities
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締切: 31-12-2025

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