Description

In this role, you will engage in method development and optimization for pharmaceutical processes, collaborating with teams to ensure quality and efficiency. Your work will blend laboratory experiments with documentation, making a significant impact on healthcare advancements.

Requirements

• •University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
• •At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
• •Advanced knowledge within the area of Analytical Development
• •Expertise in Biologics DS and DP process development applying QbD principles
• •Excellent collaboration skills
• •Proficiency in oral and written English; German is beneficial
• •Strong proficiency in digital technologies
• •Comfortable working in a hybrid environment

Tasks

• •Plan and document physical chemical method development, such as HPLC and CE
• •Ensure compliance with internal quality standards and HSE requirements
• •Utilize software tools to enhance efficiency in analytical processes
• •Support the implementation and transfer of analytical methods to teams and partners
• •Collaborate with internal laboratories and cross-functional teams for analytical workflows
• •Design and execute physicochemical analytical approaches for DS, DP, and process intermediates
• •Interpret analytical results and apply data solutions to improve efficiency
• •Lead root cause investigations and resolve complex issues
• •Author and review scientific reports and support regulatory submissions
• •Act as an analytical expert during audits and inspections
• •Manage multiple priorities and communicate challenges proactively
• •Promote knowledge sharing and present results internally
• •Contribute to publications, presentations, and patents
• •Evaluate new analytical technologies and develop innovative methods
• •Align methods with scientific standards and contribute to digitalization efforts

Benefits