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Analytical Methods Transfers Engineer (M-F)

On Friday, July 31,

Offer criteria

  • Ingénieur (H/F)
  • Waterloo (WBR)
  • CDI
  • Temps Plein
  • Industry: Industries Cosmétique, Pharma et Biotech
  • Required experience: 1-2 ans
  • Fields of expertise: Technical Writing , Laboratoire , Approach , Protocole , Scope See more , AUDIENCE , Quality systems , Corporate , Sciences de la la vie , Consulting , Leader , Legal , Playback , Audit , Biotechnologie , Design , Régulation , Assistance , Appareil médical , ADOPTION , Interpretation , Career management , LAB , Support , Pharmaceutique , Echéance , cosmétique , Regulatory Requirements , Multiples , Investigation , Health , Android , Gxp , Milieu industriel , Food & Beverage Show less
  • Preferred languages: Anglais


A Life Sciences specialist for over 20 years, CVO-EUROPE offers consulting, audit, and training services that are compliant with the regulatory requirements of the Chemical, Pharmaceutical, Biotechnology, Cosmetics, Food & Beverage, and Medical Devices industries.
With more than 350 consultants, CVO-EUROPE provides expertise in every activity that may affect patient health, product quality or data integrity.
CVO-EUROPE is an international group with business divisions in France, Belgium, Switzerland, and the USA.

Job description

Analytical Methods Transfers Engineer (M-F)

To support our development, we are looking for :

Analytical Methods Transfers Engineer (M-F)

Permanent contrac


- Contribute to technical feasibility analysis of complex research and design concepts.
- Independently plan and execute a series of design and/or technical tasks that may not be well-defined, have multiple variables and require advanced techniques within negotiated deadlines.
- Play a lead role in the evaluation, selection and adaptation of various techniques, which accomplish business objectives such as quality and cycle-time. - Write protocols and reports for scientific studies.
- Routinely provide advice and assistance to team members regarding unique problems.
- Propose new approaches to complex problems through adaptations and modifications of standard technical principles.
- Prepare activity schedule within area of competence.
- Play in active role whenever member of team whether Project Core team, Investigation team, Harmonization team, …
- In addition to having an in-depth knowledge and understanding of GxP and related regulations and guidance, is able to provide expert insights into such regulations so as to facilitate efficient product registration and/or is an active participant in the generation, review, adoption and interpretation of such regulations.
- Adhere to the Quality System, understand and apply applicable corporate, divisional and departmental procedures as relevant.

Profile description


- Possess relevant laboratory/technical/writing and computer skills.
- Ability to organize and communicate complex information that engages a large audience.
- Utilize a logical and methodological approach to help solving problems, developing solutions and making recommendations.
- Ability to make decisions even if provided with limited information.
- Ability to articulate customer needs and incorporate into work.
- Ability to make routine decisions independently.
- Ability to design experiments and draw meaningful conclusions from lab data.
- Contribute to efforts beyond own scope of responsibility to ensure project milestones are met.
- Ability to communicate effectively.

* An international Leader Company in the Engineering, Validation and Quality sector, which offers you interesting project.
* A strong corporate culture ensuring a personal and professional blooming and selffulfillment.
* Overall trainings and a personal career management.
* A good salary package with lot of extra legal advantages.

Reference: CVO/BE/ING/1_998940

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