We are looking for a highly motivated Contractor who is inspired by the unmatched opportunity to help transforming patients’ lives.In this laboratory-based position, you will work together with proficient experts in Gas Chromatography (GC), Good Manufacturing Practices (GMP) and analytical development to deliver robust and reliable test methods for purity determination in Raw Materials, Starting Materials, Intermediates, Active Pharmaceutical Ingredients and Drug Products. As such, you will contribute to ensuring the safety of our patients when launching the next “hope-in-a-box”.
Key Responsibilities:
* Coordinate and execute analytical gas chromatographic work, including method development, validation and transfer, to endorse the necessary quality attributes for the projects in scope
* Contribute to the expansion of the team’s analytical expertise towards new modalities
* Actively participate in assessing and implementing newly marketed GC methodologies and equipment
* Independently manage assigned projects in line with the project and team deliverables
* Apply state-of-the-art knowledge to ensure quality of the delivered results during investigations and troubleshooting efforts
* Ensure compliance with regulatory requirements, GMP and safety
* Guarantee accurate GMP documentation and review of generated data, along with protocol and report writing
Qualifications
Education:
* Bachelor’s or Master’s Degree in chemistry, analytical chemistry, biomedical laboratory technology or any related fields is required. A minimum of 2 years of academic or industry experience is preferred
Experience and Skills:
Required:
* Ability to work independently as well as in a team environment
* Excellent communication skills, both verbally and written
* Results and performance driven
Preferred:
* Technical knowledge of gas chromatographic systems
* Expertise in gas chromatography associated method development, validation and transfer in support of API process research, in-process control and GMP investigational testing
* Working understanding of laboratory operations and practices
* General awareness of cGMP regulations and practical experience in the implementation of those regulations
* Proficient in English, both oral and written
* Ability to work in a dynamic environment