Requirements: English
Company: ALTEN Belgium
Region: Ghent , Flanders
ALTEN Belgium is a leading consultancy company in the fields of Life Sciences, Engineering 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. This can be done with the help of our ALTEN Academy, but also through our knowledge sharing events.
All employees together form a large network of expertise, even at an international level. In this way we offer optimal growth to our consultants and the best solutions for our customers.
We are currently looking for an Analytical Development (AD) Lab Specialist at one of our clients.
We are seeking a skilled and detail-oriented Analytical Development Lab Specialist to support method development and validation for small molecules drug products. This role plays a crucial part in ensuring the quality and compliance of pharmaceutical compounds by developing and validating robust analytical techniques in line with ICH and GMP standards.
Main responsibilities
1. Method Development & Validation
- Develop and validate analytical methods using HPLC, UPLC, and GC.
- Troubleshoot and optimize analytical methods to improve reliability and performance.
2. Documentation & Reporting
- Draft validation protocols for review by research chemists and QA.
- Compile validation reports summarizing procedures, parameters, results, chromatograms, and conclusions on method suitability.
- Ensure documentation complies with GMP standards.
3. Support for QC & In-Process Controls (IPC)
- Collaborate closely with research chemists and serve as a link between analytical development, QC, and R&D teams.
- Conduct experimental tests to support method development and validation.
4. Method Testing & Optimization
- Assess and refine analytical methods based on internal and client-defined acceptance criteria.
- Work in partnership with clients to meet specific project requirements.
Your profile
- Educational background in chemistry, pharmaceutical sciences, or a related field (Masters or equivalent preferred).
- Experience in analytical method development and validation in a GMP-regulated environment.
- Hands-on experience with chromatographic techniques and software.
- Strong documentation, organizational, and communication skills.
- Ability to troubleshoot technical issues and optimize methods effectively.
- A team player with a proactive mindset and attention to detail.
What ALTEN has to offer
- A permanent contract
- A salary package in line with your experience and extra benefits (company car, meal vouchers, recovery days, insurances)
- The possibility to join a great team and be part of the success story of an international group
Apply now and be a part of our amazing journey. We believe in growing together!
We are looking forward to getting to know you and your ambitions!