Phys-chem Lab Analytical Scientist (6994)
Phys-chem Lab Analytical Scientist
12 months 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, interpretate 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