Phys-chem Lab Analytical Scientist
12 month contract with possible extension
Fully on site in Visp
Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a Phys-chem Lab Analytical Scientist for an initial 12 month contract (Maternity cover) with possible extension due to the high workload, based in the Valais area, Switzerland.
The Phys-chem Lab Analytical Scientist plays a critical role:
* Support the analytical activities required for producing information and documentation suitable for clinical development up to Process Validation stage products with particular focus on method suitability assessment/validation/verification/transfer in accordance with GMP, ICH guidelines and quality system.
* Build up a strong scientific knowledge on physical and chemical technologies with particular focus on pharmacopeia requirements and global alignment.
Main Responsibilities:
* Promote the technical innovation, scientific understanding and best practices
* Design and perform experiments, interpret results and review data for physical and chemical techniques to support method implementation/validation/verification/transfer.
* Prepare validation/transfer protocols/reports and procedures related to physical and chemical test methods. Collect and evaluate scientific data to take conclusions based on them.
* Summarize and communicate high quality information to customers and team members
* Provide troubleshooting and training support for analytical method and instruments
* Collaborate in the optimization of laboratory processes and corrective measures
* Collaborate and lead laboratory investigations, Change request and CAPA implementation
* Serves as Subject Matter Expert for the physical and chemical techniques
* Coordinate projects tasks correlated to Analytical science team
Qualifications and Experience:
* Relevant working/residency permit or Swiss/EU-Citizenship required
* Bachelor’s or Masters in relevant field.
* 5+ years of experience in Pharma industry /GMP/ transfer and validation.
* Proven experience working on GMP-compliant projects, including change management and qualification activities.
* Excellent soft skills: Flexibility, critical thinking, customer service, communication
* LIMS, Trackwise, DMS
* Business Fluent English, German is a plus
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