Description

In this role, you will evaluate and validate analytical test methods while ensuring compliance and effective communication with stakeholders. Your daily responsibilities will include troubleshooting, managing risks, and driving continuous improvement initiatives.

Requirements

• •BSc/MSc in analytical chemistry, biochemistry, or related field
• •Extensive working experience in research/technical role in pharmaceutical or chemical industry
• •Proven track record in applying analytical methods in QC or GMP regulated laboratory
• •Advanced scientific knowledge of physico-chemical analytical methods
• •Expert experience with laboratory specific software (e.g. CDS Empower)
• •Advanced knowledge in reporting, interpretation, and documentation of scientific results
• •Good communication and interpersonal skills
• •Ability to work independently and in a team
• •Good knowledge of written and spoken English

Tasks

• •Evaluate new analytical test methods during pre-validation activities
• •Transcribe test methods according to Lonza requirements
• •Support laboratory setup by ordering necessary materials
• •Conclude validation, transfer, or verification independently
• •Plan and document protocols and reports
• •Communicate efficiently to align with internal and external stakeholders
• •Manage stakeholder relationships and communicate validation risks
• •Ensure compliance and maintain up-to-date training status
• •Assist in investigations and propose mitigation measures
• •Initiate and participate in improvement initiatives

Tools & Technologies

Benefits