Associate Scientist at Nijmegen, Gelderland

Associate Scientist

For our client in biopharma, we are looking for an Associate Scientist to support laboratory activities focused on new product development, improvement of existing products, and troubleshooting in a regulated environment. You will work in a team-oriented setting where safety, quality (GLP/GMP) and continuous improvement are key.

The role

As an Associate Scientist, you execute lab work based on general guidelines and instructions, while taking ownership where possible. You document results accurately, spot deviations early, and contribute to improving methods, processes and daily lab operations.

Key responsibilities

Project-based work

• Discuss assignments and planning with Project Leader(s)
• Design and perform experiments using existing methods where applicable
• Set up test designs and coordinate supporting activities (materials, prep work, planning)
• Execute standard lab preparations and tests
• Identify deviations, investigate root cause and propose improvements to experimental design
• Record, interpret and discuss results with the project team
• Write clear documentation such as Subject Memos, Subject Reports, and Protocols/Regulations (sometimes in English)
• Perform operational activities under GxP, e.g. support of:
• pilot and consistency batches
• small-scale batches for animal studies
• seed productions
• Propose and help introduce new methods and techniques
• Support transfer of processes and QC tests to Production and QC (when applicable)

Daily lab / department activities

• Support day-to-day lab operations, including GxP and EHS requirements
• Maintain a strong safety-first mindset
• Contribute to continuous improvement initiatives
• Support introduction, qualification and maintenance of new equipment
• Help onboard and train new employees and/or trainees (if needed)

Requirements

• Relevant HBO education and/or equivalent experience
• Knowledge of laboratory setup and operations (standards, rules, good documentation practices)
• Hands-on experience working according to GxP guidelines (GLP/GMP)
• Knowledge of and experience with MPS methods
• Comfortable working in a structured, regulated environment with strong attention to detail

Klaar voor de volgende stap?

Solliciteer direct via “Solliciteren” of stuur je cv en motivatiebrief naar:

Audrey Poluakan - Recruitment Consultant Life Sciences

E: audrey.poluakan@gigroup.com

M: 0658069570