Analytical Development Analyst
Brabant Wallon – Contracting
What are your responsibilities?
This team’s primary responsibility is to develop, validate and transfer to internal and external partners, robust and efficient physico-chemical methods, according to the required regulatory requirement standards. The team also provides analytical support and expertise to process understanding and process validation of biological and chemical processes and is responsible for transferring methodology, technology, data and preparing regulatory submissions with business partners.
Scope of the mission:
The primary goal of the mission is to provide scientific expertise to contribute to contribute to manage physics-chemical method development activities from early clinical phases to commercial.
The main techniques used are Liquid chromatography (Size-exclusion, Reverse-phase, affinity, Ion exchange, HILIC or HIC) or electrophoresis capillary (CzE).
Major accountabilities:
The main activities of this position will be:
- Design experiments
- Autonomously manage and perform daily laboratory activities related to method development, validation, transfers
- Contribute to release and stability testing related to the project as appropriate.
- Prepare and review/approve documentation (procedures, protocols, reports)
- Analyze results.
- Verify data.
- Present/discuss results in project team meetings.
All these activities will be performed in compliance with the GMP/HSE rules and with the regulatory requirements for each development phase of the product.
Who are you?
- Master’s or bachelor’s degree in biochemistry or in analytical chemistry
- At least 5 years of experience in the pharmaceutical industry
- Strong and proven laboratory skills
- Good knowledge of protein chemistry and techniques for separating polymers in a protein matrix
- A good practical experience and expertise in at least one of the analytical techniques used in the laboratory: chromatography (Size-exclusion, Reverse-phase, affinity, Ion exchange, HILIC or HIC) or electrophoresis capillary (CzE)
- Expertise in analytical method development and validation
- Ability to author and review comprehensive and accurate procedures, protocols, and reports.
- A good knowledge of GLP/GMP rules.
- A good level of English is recommended for reports and oral communication.
- Ability to handle multiple priorities and/or prioritization.
- Interpersonal skills to communicate and maintain good working relationships within the team and with internal/external customers/partners.
- Ability to work in a matrix and customer-oriented environment.
Our Offer?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.